Team:Harvard/Human Practices

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__NOTOC__
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=Intellectual Property and Open Source Technology=
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We have explored the <b>[[#The History of IP and Open Source in Zinc Finger Technology|history]]</b> and associated intellectual property (IP) issues that have surrounded zinc finger technology.
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==The History of Zinc Fingers: A Case Study in Intellectual Property==
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Because teams are trying to solve real-world problems, the vast majority of iGEM projects intersect with the IP landscape. Aside from its immediate relevance to our project, we argue that the story of zinc finger discovery, development, and commercialization presents a useful and enlightening <b>[[#No_.22Finger.22_Pointing|case study]]</b> of how IP affects the synthetic biology community.
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Discovered in 1985, zinc finger proteins have rapidly become a staple of gene therapy innovation. A cascade of research has transformed our understanding of the zinc finger domain from a natural transcription factor to a tool for highly specific genome alteration. As the zinc finger motif was domesticated and fused to DNA cleaving domains, its practical application to gene therapy through targeted gene alteration was realized. Seeking to harness zinc finger potential, researchers and entrepreneurs collaborated to form Sangamo Biosciences in 1995, which emerged as the sole commercial provider of the protein. Today, the Sangamo monopoly raises a variety difficult ethical and economic questions about intellectual property within the zinc finger field, and synthetic biology as a whole. As an open-source alternative to Sangamo’s proprietary system and commercial dominance, Keith Joung and others have published the OPEN system of zinc finger creation. However, while the OPEN system and subsequent improvements are promising for massive zinc finger production, the methods are difficult and time-consuming to implement, and gaps remain in the list of available DNA binding targets.  
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Additionally, we wrote and sent a '''[https://2011.igem.org/Team:Harvard/Human_Practices/Letter letter]''' to multiple representatives regarding the conflict between IP and open source technology.
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==The History of IP and Open Source in Zinc Finger Technology==
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Discovered in 1985, zinc finger proteins have rapidly become a staple of gene therapy innovation. A cascade of research has transformed our understanding of the zinc finger domain from a natural transcription factor to a tool for highly specific genome alteration. As the zinc finger motif was domesticated and fused to DNA cleaving domains, its practical application through targeted gene alteration rose to the forefront of gene therapy research.
 +
 
 +
Seeking to harness zinc finger potential, researchers and entrepreneurs collaborated to form Sangamo Biosciences in 1995, which emerged as the sole commercial provider of the protein. Today, the Sangamo monopoly raises a variety difficult ethical and economic questions about intellectual property within the zinc finger field, and synthetic biology as a whole. As an open-source alternative to Sangamo’s proprietary system and commercial dominance, Keith Joung and others have published the OPEN system[[#References|[5]]] of zinc finger creation. However, while the OPEN system and subsequent improvements are promising for massive zinc finger production, the methods are difficult and time-consuming to implement, and gaps remain in the list of available DNA binding targets.
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===Zinc Finger Historical Timeline===
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<li><a href="#" class="dateobject">1985</a></li>
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<li><a href="#" class="dateobject">1991</a></li>
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<li><a href="#" class="dateobject">1995</a></li>
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<img src="https://static.igem.org/mediawiki/2011/c/cb/HARV1985Miller_etal.png" width="256" height="256" />
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<div class="issuedate">Discovery of the zinc finger protein</div>
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<p>Jonathon Miller, A. D. McLachlan, and Sir Aaron Klug first identify the repeated binding motif in Transcription Factor IIIA and are the first to use the term ‘zinc finger.'</p>
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<li id="#1991">
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<img src="https://static.igem.org/mediawiki/2011/7/76/HARVzif268_256.png" width="256" height="256" />
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<div class="issuedate">First crystal structure of a zinc finger</div>
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<p>Carl Pabo and Nikola Pavletich of Johns Hopkins University solve the crystal structure of zif268, now the most-commonly studied zinc finger. This paved the way for construction of binding models to describe how zinc fingers bind to DNA, setting the foundation for future custom engineering of zinc finger proteins.</p>
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<li id="#1995">
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<img src="https://static.igem.org/mediawiki/2011/4/49/HARVSangamo.png" width="256" height="256" />
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<div class="issuedate">CEO Edward Lanphier founds Sangamo Biosciences</div>
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<p>Edward Lanphier leaves Somatix Therapy Corporation and makes a deal for exclusive rights to the work of Srinivan Chandrasegaran of Johns Hopkins University who combined the Fok I nuclease with zinc fingers.</p>
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<img src="https://static.igem.org/mediawiki/2011/7/73/HARVZFN_diagram_256.png" width="256" height="256" />
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<div class="issuedate">Srinivasan Chandrasegaran publishes work on fusing the Fok I nuclease to zinc fingers</div>
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<p>By attaching nuclease proteins to zinc fingers, a new genome editing tool was created. The DNA-binding specificity of zinc fingers combined with the DNA-cutting ability of nucleases opened up possibilities for future research in gene therapy by allowing researchers to directly modify the genome though use of zinc finger nucleases.</p>
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<img src="https://static.igem.org/mediawiki/2011/5/5e/HARVStockSGMO_256.PNG" width="256" height="256" />
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<div class="issuedate">Sangamo enters the public sector</div>
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<p>In April 2000, five years after its founding, Sangamo Biosciences goes public offering 3.5 million shares at a starting value of $15 per share.</p>
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<div class="issuedate">Sangamo patents zinc finger nuclease technology</div>
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<p>Sangamo's patent, titled "Nucleic acid binding proteins (zinc finger proteins design rules)", ensures that any use or production of zinc fingers with attached nucleases is the intellectual property of Sangamo.</p>
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<img src="https://static.igem.org/mediawiki/2011/6/67/HARVOpen_256.png" width="256" height="256" />
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<div class="issuedate">Rapid open source production of zinc finger nucleases becomes available</div>
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<p>Researcher Keith Joung of Harvard University and Mass. General Hospital develops a method for making zinc finger nuclease proteins that bind to custom target sequences, utilizing a bacterial two-hybrid screening system to identify specific zinc finger binders to a DNA sequence of interest.</p>
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<img src="https://static.igem.org/mediawiki/2011/8/87/HARVClinicaltrial_256.png" width="256" height="256" />
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<div class="issuedate">Zinc finger nuclease enters clinical trials</div>
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<p>Sangamo and University of Pennsylvania begin clinical trials with a zinc finger nuclease designed to target the CCR5 gene and inhibit HIV. Success of this therapeutic could prove a significant advance for gene therapy. </p>
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<div class="issuedate">Context-dependency improves open-source zinc finger engineering</div>
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<p>Keith Joung publishes tables of zinc finger binding sites that account for context-dependent effects and can be rearranged to form custom zinc finger proteins that bind to a variety of DNA sequences. This greatly increases the ease of engineering novel zinc fingers based on the structures of previously characterized zinc fingers.</p>
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<div class="issuedate">Harvard iGEM develops a novel method to engineer custom zinc fingers</div>
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<p>Using novel integration of existing technologies, we have developed a rapid, comparatively low-cost, <strong>open source</strong> method for making thousands of custom zinc fingers by integrating MAGE, lambda red, and chip-based synthesis technologies. Our work greatly increases the ease of access to zinc finger technology for researchers worldwide.</p>
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==Harvard iGEM and Human Practices==
==Harvard iGEM and Human Practices==
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Where does our project stand in this complex and contentious history? Through the novel application and integration of existing technologies, we seek to provide a streamlined method for zinc finger production which allows rapid creation of custom zinc fingers in a high-volume fashion for targeting novel binding sequences. This has allowed us to fill gaps of undiscovered zinc finger binders in the OPEN and CoDA database and other open-source zinc finger databases. Most importantly, our open-source BioBrick materials and protocols greatly increase the accessibility of zinc fingers: our foundational advance helps to overcome the prohibitively high prices of the present market. We aim to increase the accessibility of our method, which can in turn be applied to the generation of novel biological interactions beyond zinc fingers.
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===Where does our project stand in this complex and contentious history?===
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The objective of our project was to provide an open-source, "reduced-to-practice" method for zinc finger production through the novel application and integration of technologies. This method allows for the rapid creation of custom zinc fingers in a high-volume fashion for targeting novel binding sequences. This, in turn, has enabled us to fill gaps of undiscovered zinc finger binders in the OPEN and CoDA[[#References|[4]]] database and other open-source zinc finger databases. Most importantly, our open-source [https://2011.igem.org/Team:Harvard/Results/Biobricks BioBrick materials], [https://2011.igem.org/Team:Harvard/Protocols detailed protocols], and [https://2011.igem.org/Team:Harvard/Results/Tools software tools] greatly increase the accessibility of zinc finger technology and help to overcome the prohibitively high price tags of the present market.  
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We aim to increase the accessibility of our method, which can in turn be applied by others to the generation of novel biological interactions beyond zinc fingers. We wish to share our data and results with the community, highlighting our successes and failures to collectively advance our knowledge of designing novel biological interactions. In addition, we seek to openly address pertinent ethical and legal concerns surrounding the impact of intellectual property in synthetic biology, and to open a dialogue to raise awareness about these issues.
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==Safety==
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While ZF nucleases are highly promising tool for gene therapy, significant concerns about the safety of its usage on humans remain. The concerns primarily stem from the off-target effects of ZF nucleases. Even a modest off-target effect could result in multiple double strand breaks on the genome leading to high genomic instability, potentially causing effects worse than the original defect.
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=No "Finger" Pointing=
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==A Case Study in Intellectual Property and Open Source Alternatives==
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Two approaches that would help mitigate this:
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'''The Harvard iGEM team aims to open discussion and raise awareness of the future impacts of intellectual property rights on synthetic biology research. We seek to provide an objective view of the existing relationships between intellectual property and open-source content. Our concern is particularly for the necessity of balance in intellectual property rights and the promotion of open-source technology for optimal benefit to all.'''
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===iGEM & IP===
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The questions raised by this case study are of particular importance for synthetic biology, which has historically placed great emphasis on an open-source nature. iGEM in particular has placed great value on this history. The Registry of Standard Biological parts and the concept of BioBricks are fundamental examples: characterized, standardized parts are available to on the [http://partsregistry.org registry website] to anyone with Internet access. In fact, IP questions are relevant for many of the technologies developed and used in the competition.
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===Playing Monopoly===
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Zinc finger intellectual property is held predominantly by a single commercial research institution, unlike many other areas of research where intellectual property is distributed across a wide variety of interested parties. This institution, [http://www.sangamo.com/index.html Sangamo Biosciences Inc.], is a clinical stage biopharmaceutical company which focuses on zinc finger production for clinical applications. Sangamo has acquired most of the patent rights for the exclusive production and use of zinc finger proteins as DNA-modifying molecules. The result is an imbalance in the legal rights to research zinc fingers and their related medical applications which has notable consequences.
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<div id="ip_quote">"Scientists who purchase zinc fingers... must sign a license that imposes certain restrictions. To prevent scientists from selling or even sharing ZFNs, there’s a limit to how many animals can be produced [that express the zinc finger nuclease]. Nor can a scientist share anything made using the zinc fingers outside her organization."</div></html>
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[[File:HARVSangamo_Patent_Timeline.png| right|425px|Ownership (assignees) of US ZFP patents by institution, 1993–2007 [[#References|[2]]].]]
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===Implications of Monopoly===
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====Opposition====
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First, researchers outside of Sangamo may be less motivated to research zinc finger technology because there is less of a foreseeable reward with patent rights blocking any prospect of earning a profit from patenting new technology. Even if there is no profit motive involved, it is impossible to do open source research using purchased zinc fingers, as licensing and high costs inhibit effective research. [[#References|[3]]] The cost of purchasing a single zinc finger protein from Sigma® Life Science (licencing partner with Sangamo) is prohibitively high - up to $15,000 for a single functioning zinc finger nuclease, which only work as pairs [[#References|[3]]] - limiting the possibilities for significant outside research.
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====In Favor====
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Second, Sangamo is able to monopolize the zinc finger market and intellectual capital: this means that they become a powerful, specialized research institution with the ability to potentially achieve progress at a faster pace than multiple individual institutions. Specialization naturally allows Sangamo to make progress more efficiently than individual researchers. Centralization also brings specialized researchers together under one roof for effective collaboration without having to cross communication barriers that exist between multiple isolated institutions.
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====Forward====
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These two effects act in opposite directions from the perspective of making intellectual progress for humanity. Thus we arrive at the central question: Does the Sangamo zinc finger monopoly augment the positive effects of research benefits for humanity and profit for individual researchers? Is the Sangamo research monopoly more beneficial to all involved parties?
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===In Favor of Opening the Field===
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====Imbalance of Research Benefits====
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The economic consequences of monopoly have been posed by some as a clear negative consequence of the Sangamo phenomenon. In a single-actor monopoly, standard economic theory predicts that the rational market actor will sell at the profit-maximizing price. This price, however, does not necessarily maximize social benefit especially since monopolistic trade results in deadweight loss [[#References|[1]]]. In other words, this means that the collective world production of societal benefits - such as medical treatments - potentially decreases in order to maximize profit for Sangamo.
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====Technology Vacuum====
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Lack of transparency in the field inhibits outside research while promoting Sangamo’s internal research. Technology that otherwise would have been available for use by many researchers is concealed behind Sangamo's large patent portfolio. Therefore, Sangamo passively impedes outside research by removing the opportunities for advancement and dissemination of protocols.
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====Risk of Centralization and Failure====
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Another problem with the monopolistic model arises when the company fails: when it fails to make scientific progress, and the whole field suffers. Recently, Sangamo Biosciences’ lead drug candidate has flunked its biggest test yet in clinical trials, and the company said this morning [October 3 2011] that it’s time to move on to other programs.[Sangamo] said today that SB-509 failed in a study of 170 patients that randomly assigned patients with diabetic neuropathy to a new drug or a placebo." [[#References|[8]]] If concerns of IP violation discouraged other researchers from working on comparable zinc finger-based treatments for that disease, there is now nothing to show for years of work, and the disease remains untreatable from a gene therapy approach.
 +
[[File:HARVProtoMag Table.png| left| 350px |Making zinc fingers: monetary and time investments [[#References|[3]]].]]
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===Two Sides to Every Story: Benefits of IP===
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====Intellectual Property Security====
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However, others have argued that concentrating intellectual property in a single company has actually promoted innovation and progress in the field [[#References|[2]]]. Monetary incentive to conduct research is undoubtedly a key driving force for scientific progress. What scientist or institution would invest in research without at least a chance of returning profit? Lack of protection of intellectual property rights and thus profit would diminish the sense of security and equality that the U.S. patent system currently provides. In fact the U.S. patent system was first instated to encourage openness of knowledge. Sangamo's large patent share gives the impression that intellectual property rights block future research incentive. In fact without intellectual property rights zinc finger research (and Sangamo) may not even exist today.
 +
 
 +
====Centralization Boosts Efficiency====
 +
By bringing leaders in the field together, Sangamo might allow zinc finger researchers to be more productive through close collaboration than they otherwise would have been working individually. Furthermore, specialization in zinc finger technology minimizes costs of production that individual researchers would otherwise face. From the perspective of consumers purchasing zinc fingers, valuable time and negotiation costs may be saved by working with one company rather than many.
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 +
===Conclusion: Striking a Balance===
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The ultimate goal of both Sangamo and other researchers is to make progress in scientific innovation while gaining profit from intellectual property. Naturally both Sangamo and other science researchers will tend to maximize personal profit; however, we suggest that the optimal scenario would maximize both scientific progress and the collective profit gained by each research actor.
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===The Harvard iGEM Proposition===
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An optimal resolution can be achieved only by a proper balance between intellectual property right regulation and open source technology; therefore we propose that there be an investigation into the current status of the zinc finger intellectual market with respect to the social and private profit-maximizing values. Currently the market lies heavily in favor of maximizing the private profits for Sangamo and the chance that this is the overall profit-maximizing equilibrium is therefore lessened. Only by properly informing the scientific community of the implications of imbalance between intellectual property rights and open source technology can we hope to achieve the most efficient research conditions for the future of synthetic biology research.
 +
 
 +
One way to do this would be to follow the model of the European Union. In most European countries, patent laws "include a 'research exception' which permits use of  a patented invention for experimental purposes without infringing the rights of the holder. Additionally, there are further exceptions such as those in respect of private and non-commercial use." [[#References|[7]]] In the United Kingdom, specifically,  "those acts which do not constitute an infringement are set out in Section 60(5) of the Patents Act 1977."[[#References|[7]]] How can the United States remain competitive in the long-term with countries who allow for academic research without fear of infringement - and have done so for the past 30 years? 
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A research exception could provide the needed balance between IP and research: companies could maintain their profitability, while scientists could use the best methods and ideas in their academic research, without fear of litigation.
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[[File:HARVMegaphone2 GROUPED.png| left| 100px]]
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=<div style="text-align:center">For more information on Harvard iGEM's Human Practices activism,</div>=
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=<div style="text-align:center">visit http://harvardigem.org/</div>=
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1. Explicitly design against non-specific sequences:
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=References=
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As we design novel ZF proteins towards a sequence, it is essential to negatively design against all closely related sequences to reduce off-target effects. Further, it may be wise to compromise on binding affinity for higher
+
'''1.''' Mankiw, G. (2012). Principles of Economics. New York: South-Western Cengage Learning.
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specificity.
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2. Design zero nuclease activity of the monomer – obligate dimer requirement:
+
'''2.''' Chandrasekharan, S., Kumar, S., Valley, C., & Rai, A. (2009). Proprietary science, open science and the role of patent disclosure: the case of zinc-finger proteins. Nature Biotechnology, 140-144. [http://www.nature.com/nbt/journal/v27/n2/full/nbt0209-140.html#B36]
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In order to induce a double strand break, two ZF arrays each attached to a FokI domain bind to a dsDNA. The FokI domains need to homodimerize to perform nuclease activity. However, low levels of FokI monomer nuclease activity could result in double strand breaks at unintended locations wherever a single ZF array-FokI chimera transiently binds. To reduce such background effect, a FokI domain (or other nuclease domains) have to be designed with zero monomer  activity.
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==Ethics==
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'''3.''' Gorman, R. (2010, Fall). Zinc Fingers: Entry Fee. Proto: Massachusetts General Hospital, Dispatches from the Frontiers of Medicine, pp. 35-39. [http://protomag.com/assets/zinc-fingers-entry-fee]
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Important ethical issues surround therapeutic application of ZF nuclease based gene therapy. The efficacy of gene therapy could be offset by the poorly understood side effects of ZF nucleases. For instance, it is now known that deletion of CCR5 gene confers resistance to HIV. Therefore, efforts are underway to design ZF nucleases targeted to the CCR5 locus for deleting the gene. While this may certainly benefit fight against HIV, the side effects could cause a different, but just as fatal, illness. Enhanced oncogenicity could result from multiple off-target double strand
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'''4.''' Jeffry D Sander, Elizabeth J Dahlborg, Mathew J Goodwin, Lindsay Cade, Feng Zhang, Daniel Cifuentes, Shaun J Curtin, Jessica S Blackburn, Stacey Thibodeau-Beganny, Yiping Qi, Christopher J Pierick, Ellen Hoffman, Morgan L Maeder, Cyd Khayter, Deepak Reyon, Drena Dobbs, David M Langenau, Robert M Stupar, Antonio J Giraldez, Daniel F Voytas, Randall T Peterson,Jing-Ruey J Yeh, J Keith Joung. Selection-free zinc-finger-nuclease engineering by context-dependent assembly (CoDA)(2011). ''Nature Methods'' 8, 67–69. [http://www.nature.com/nmeth/journal/v8/n1/full/nmeth.1542.html]
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breaks caused by ZF nucleases. Should we deny HIV therapy because of unknown side effects of the therapy? Or, is it okay to knowingly administer the therapy at the patient’s behest after he/she has been sufficiently educated? Dialogue on such ethical issues needs to progress in parallel with development of the therapy itself.
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==Ownership and Sharing==
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'''5.''' Morgan L. Maeder, Stacey Thibodeau-Beganny, Anna Osiak, David A. Wright, Reshma M. Anthony, Magdalena Eichtinger, Tao Jiang, Jonathan E. Foley, Ronnie J. Winfrey, Jeffrey A. Townsend, Erica Unger-Wallace, Jeffry D. Sander, Felix Müller-Lerch, Fengli Fu, Joseph Pearlberg, Carl Göbel, Justin P. Dassie, Shondra M. Pruett-Miller, Matthew H. Porteus, Dennis C. Sgroi, A. John Iafrate, Drena Dobbs, Paul B. McCray Jr., Toni Cathomen, Daniel F. Voytas, J. Keith Joung. Rapid “Open-Source” Engineering of Customized Zinc-Finger Nucleases for Highly Efficient Gene Modification (2008). ''Molecular Cell'' Volume 31, Issue 2, 25 July 2008, Pages 294-301.[http://www.sciencedirect.com/science/article/pii/S1097276508004619]
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The objective of our project was to present an open-source technology for development of ZF proteins for any desired target sequence. Companies like Sangamo develop custom ZF proteins for your-favorite-gene at a price tag that is
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'''6.''' Christopher Thomas Scott. The zinc finger nuclease monopoly. ''Nature Biotechnology'' Vol23 Num8, 2005.[http://www.cambia.org/daisy/cambia/1186/version/default/part/AttachmentData/data/'The_zinc_finger_nuclease_monopoly'.pdf]
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unaffordable to most academic laboratories. Here we showcase a nearly “reduced-to-practice” method with detailed protocols for any academic laboratory to repeat our method for their target sequence of choice. We wish to share our data and results with the community, highlighting our successes and failures to collectively advance of our knowledge of designing novel
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ZF proteins.
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==Innovation==
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'''7.''' UK Intellectual Property Office. The Patent Research Exception: A Consultation. 2008.[http://www.ipo.gov.uk/consult-patresearch.pdf]
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Our innovation lies in bringing together many technologies to create a general open-source method for designing novel ZF proteins. The plasmid-based one-hybrid selection system was previously known; we applied lambda-red recombineering to
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'''8.''' Luke Timmerman. Sangamo Fails Diabetic Neuropathy Study, Falls Back on HIV, Other Programs. ''Xconomy'', 10/3/11. [http://www.xconomy.com/san-francisco/2011/10/03/sangamo-fails-diabetic-neuropathy-study-falls-back-on-hiv-other-programs/]
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integrate the selection system on the genome in order to reduce background due to copy number variation of the plasmids. Chip-based DNA synthesis was previously developed a cheap source of DNA; we applied it towards generating nearly 55,000 designed ZF proteins. Our bioinformatics pipeline combined structure-based information and experimental binding data to develop frequency distribution tables for forward engineering. MAGE technology enabled facile genome modification without the need for a selection marker and allowed us to disable E.coli hisB and pyrF genes by inserting a stop codon.  
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With the increasing promise of gene therapy, we have uniquely combined various technologies to fulfill the unmet need for an open-source method to modify human genomes.
 
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Latest revision as of 17:14, 12 April 2012

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IP and Open Source Technology | Letter to Representatives

Intellectual Property and Open Source Technology

We have explored the history and associated intellectual property (IP) issues that have surrounded zinc finger technology.

Because teams are trying to solve real-world problems, the vast majority of iGEM projects intersect with the IP landscape. Aside from its immediate relevance to our project, we argue that the story of zinc finger discovery, development, and commercialization presents a useful and enlightening case study of how IP affects the synthetic biology community.

Additionally, we wrote and sent a letter to multiple representatives regarding the conflict between IP and open source technology.

The History of IP and Open Source in Zinc Finger Technology

Discovered in 1985, zinc finger proteins have rapidly become a staple of gene therapy innovation. A cascade of research has transformed our understanding of the zinc finger domain from a natural transcription factor to a tool for highly specific genome alteration. As the zinc finger motif was domesticated and fused to DNA cleaving domains, its practical application through targeted gene alteration rose to the forefront of gene therapy research.

Seeking to harness zinc finger potential, researchers and entrepreneurs collaborated to form Sangamo Biosciences in 1995, which emerged as the sole commercial provider of the protein. Today, the Sangamo monopoly raises a variety difficult ethical and economic questions about intellectual property within the zinc finger field, and synthetic biology as a whole. As an open-source alternative to Sangamo’s proprietary system and commercial dominance, Keith Joung and others have published the OPEN system[5] of zinc finger creation. However, while the OPEN system and subsequent improvements are promising for massive zinc finger production, the methods are difficult and time-consuming to implement, and gaps remain in the list of available DNA binding targets.

Zinc Finger Historical Timeline

  • Discovery of the zinc finger protein

    Jonathon Miller, A. D. McLachlan, and Sir Aaron Klug first identify the repeated binding motif in Transcription Factor IIIA and are the first to use the term ‘zinc finger.'

  • First crystal structure of a zinc finger

    Carl Pabo and Nikola Pavletich of Johns Hopkins University solve the crystal structure of zif268, now the most-commonly studied zinc finger. This paved the way for construction of binding models to describe how zinc fingers bind to DNA, setting the foundation for future custom engineering of zinc finger proteins.

  • CEO Edward Lanphier founds Sangamo Biosciences

    Edward Lanphier leaves Somatix Therapy Corporation and makes a deal for exclusive rights to the work of Srinivan Chandrasegaran of Johns Hopkins University who combined the Fok I nuclease with zinc fingers.

  • Srinivasan Chandrasegaran publishes work on fusing the Fok I nuclease to zinc fingers

    By attaching nuclease proteins to zinc fingers, a new genome editing tool was created. The DNA-binding specificity of zinc fingers combined with the DNA-cutting ability of nucleases opened up possibilities for future research in gene therapy by allowing researchers to directly modify the genome though use of zinc finger nucleases.

  • Sangamo enters the public sector

    In April 2000, five years after its founding, Sangamo Biosciences goes public offering 3.5 million shares at a starting value of $15 per share.

  • Sangamo patents zinc finger nuclease technology

    Sangamo's patent, titled "Nucleic acid binding proteins (zinc finger proteins design rules)", ensures that any use or production of zinc fingers with attached nucleases is the intellectual property of Sangamo.

  • Rapid open source production of zinc finger nucleases becomes available

    Researcher Keith Joung of Harvard University and Mass. General Hospital develops a method for making zinc finger nuclease proteins that bind to custom target sequences, utilizing a bacterial two-hybrid screening system to identify specific zinc finger binders to a DNA sequence of interest.

  • Zinc finger nuclease enters clinical trials

    Sangamo and University of Pennsylvania begin clinical trials with a zinc finger nuclease designed to target the CCR5 gene and inhibit HIV. Success of this therapeutic could prove a significant advance for gene therapy.

  • Context-dependency improves open-source zinc finger engineering

    Keith Joung publishes tables of zinc finger binding sites that account for context-dependent effects and can be rearranged to form custom zinc finger proteins that bind to a variety of DNA sequences. This greatly increases the ease of engineering novel zinc fingers based on the structures of previously characterized zinc fingers.

  • Harvard iGEM develops a novel method to engineer custom zinc fingers

    Using novel integration of existing technologies, we have developed a rapid, comparatively low-cost, open source method for making thousands of custom zinc fingers by integrating MAGE, lambda red, and chip-based synthesis technologies. Our work greatly increases the ease of access to zinc finger technology for researchers worldwide.

Harvard iGEM and Human Practices

Where does our project stand in this complex and contentious history?

The objective of our project was to provide an open-source, "reduced-to-practice" method for zinc finger production through the novel application and integration of technologies. This method allows for the rapid creation of custom zinc fingers in a high-volume fashion for targeting novel binding sequences. This, in turn, has enabled us to fill gaps of undiscovered zinc finger binders in the OPEN and CoDA[4] database and other open-source zinc finger databases. Most importantly, our open-source BioBrick materials, detailed protocols, and software tools greatly increase the accessibility of zinc finger technology and help to overcome the prohibitively high price tags of the present market.

We aim to increase the accessibility of our method, which can in turn be applied by others to the generation of novel biological interactions beyond zinc fingers. We wish to share our data and results with the community, highlighting our successes and failures to collectively advance our knowledge of designing novel biological interactions. In addition, we seek to openly address pertinent ethical and legal concerns surrounding the impact of intellectual property in synthetic biology, and to open a dialogue to raise awareness about these issues.

No "Finger" Pointing

A Case Study in Intellectual Property and Open Source Alternatives

The Harvard iGEM team aims to open discussion and raise awareness of the future impacts of intellectual property rights on synthetic biology research. We seek to provide an objective view of the existing relationships between intellectual property and open-source content. Our concern is particularly for the necessity of balance in intellectual property rights and the promotion of open-source technology for optimal benefit to all.

iGEM & IP

The questions raised by this case study are of particular importance for synthetic biology, which has historically placed great emphasis on an open-source nature. iGEM in particular has placed great value on this history. The Registry of Standard Biological parts and the concept of BioBricks are fundamental examples: characterized, standardized parts are available to on the registry website to anyone with Internet access. In fact, IP questions are relevant for many of the technologies developed and used in the competition.

Playing Monopoly

Zinc finger intellectual property is held predominantly by a single commercial research institution, unlike many other areas of research where intellectual property is distributed across a wide variety of interested parties. This institution, Sangamo Biosciences Inc., is a clinical stage biopharmaceutical company which focuses on zinc finger production for clinical applications. Sangamo has acquired most of the patent rights for the exclusive production and use of zinc finger proteins as DNA-modifying molecules. The result is an imbalance in the legal rights to research zinc fingers and their related medical applications which has notable consequences.

"Scientists who purchase zinc fingers... must sign a license that imposes certain restrictions. To prevent scientists from selling or even sharing ZFNs, there’s a limit to how many animals can be produced [that express the zinc finger nuclease]. Nor can a scientist share anything made using the zinc fingers outside her organization."

Ownership (assignees) of US ZFP patents by institution, 1993–2007 [2].

Implications of Monopoly

Opposition

First, researchers outside of Sangamo may be less motivated to research zinc finger technology because there is less of a foreseeable reward with patent rights blocking any prospect of earning a profit from patenting new technology. Even if there is no profit motive involved, it is impossible to do open source research using purchased zinc fingers, as licensing and high costs inhibit effective research. [3] The cost of purchasing a single zinc finger protein from Sigma® Life Science (licencing partner with Sangamo) is prohibitively high - up to $15,000 for a single functioning zinc finger nuclease, which only work as pairs [3] - limiting the possibilities for significant outside research.

In Favor

Second, Sangamo is able to monopolize the zinc finger market and intellectual capital: this means that they become a powerful, specialized research institution with the ability to potentially achieve progress at a faster pace than multiple individual institutions. Specialization naturally allows Sangamo to make progress more efficiently than individual researchers. Centralization also brings specialized researchers together under one roof for effective collaboration without having to cross communication barriers that exist between multiple isolated institutions.

Forward

These two effects act in opposite directions from the perspective of making intellectual progress for humanity. Thus we arrive at the central question: Does the Sangamo zinc finger monopoly augment the positive effects of research benefits for humanity and profit for individual researchers? Is the Sangamo research monopoly more beneficial to all involved parties?

In Favor of Opening the Field

Imbalance of Research Benefits

The economic consequences of monopoly have been posed by some as a clear negative consequence of the Sangamo phenomenon. In a single-actor monopoly, standard economic theory predicts that the rational market actor will sell at the profit-maximizing price. This price, however, does not necessarily maximize social benefit especially since monopolistic trade results in deadweight loss [1]. In other words, this means that the collective world production of societal benefits - such as medical treatments - potentially decreases in order to maximize profit for Sangamo.

Technology Vacuum

Lack of transparency in the field inhibits outside research while promoting Sangamo’s internal research. Technology that otherwise would have been available for use by many researchers is concealed behind Sangamo's large patent portfolio. Therefore, Sangamo passively impedes outside research by removing the opportunities for advancement and dissemination of protocols.

Risk of Centralization and Failure

Another problem with the monopolistic model arises when the company fails: when it fails to make scientific progress, and the whole field suffers. Recently, Sangamo Biosciences’ lead drug candidate has flunked its biggest test yet in clinical trials, and the company said this morning [October 3 2011] that it’s time to move on to other programs.[Sangamo] said today that SB-509 failed in a study of 170 patients that randomly assigned patients with diabetic neuropathy to a new drug or a placebo." [8] If concerns of IP violation discouraged other researchers from working on comparable zinc finger-based treatments for that disease, there is now nothing to show for years of work, and the disease remains untreatable from a gene therapy approach.

Making zinc fingers: monetary and time investments [3].

Two Sides to Every Story: Benefits of IP

Intellectual Property Security

However, others have argued that concentrating intellectual property in a single company has actually promoted innovation and progress in the field [2]. Monetary incentive to conduct research is undoubtedly a key driving force for scientific progress. What scientist or institution would invest in research without at least a chance of returning profit? Lack of protection of intellectual property rights and thus profit would diminish the sense of security and equality that the U.S. patent system currently provides. In fact the U.S. patent system was first instated to encourage openness of knowledge. Sangamo's large patent share gives the impression that intellectual property rights block future research incentive. In fact without intellectual property rights zinc finger research (and Sangamo) may not even exist today.

Centralization Boosts Efficiency

By bringing leaders in the field together, Sangamo might allow zinc finger researchers to be more productive through close collaboration than they otherwise would have been working individually. Furthermore, specialization in zinc finger technology minimizes costs of production that individual researchers would otherwise face. From the perspective of consumers purchasing zinc fingers, valuable time and negotiation costs may be saved by working with one company rather than many.

Conclusion: Striking a Balance

The ultimate goal of both Sangamo and other researchers is to make progress in scientific innovation while gaining profit from intellectual property. Naturally both Sangamo and other science researchers will tend to maximize personal profit; however, we suggest that the optimal scenario would maximize both scientific progress and the collective profit gained by each research actor.

The Harvard iGEM Proposition

An optimal resolution can be achieved only by a proper balance between intellectual property right regulation and open source technology; therefore we propose that there be an investigation into the current status of the zinc finger intellectual market with respect to the social and private profit-maximizing values. Currently the market lies heavily in favor of maximizing the private profits for Sangamo and the chance that this is the overall profit-maximizing equilibrium is therefore lessened. Only by properly informing the scientific community of the implications of imbalance between intellectual property rights and open source technology can we hope to achieve the most efficient research conditions for the future of synthetic biology research.

One way to do this would be to follow the model of the European Union. In most European countries, patent laws "include a 'research exception' which permits use of a patented invention for experimental purposes without infringing the rights of the holder. Additionally, there are further exceptions such as those in respect of private and non-commercial use." [7] In the United Kingdom, specifically, "those acts which do not constitute an infringement are set out in Section 60(5) of the Patents Act 1977."[7] How can the United States remain competitive in the long-term with countries who allow for academic research without fear of infringement - and have done so for the past 30 years?

A research exception could provide the needed balance between IP and research: companies could maintain their profitability, while scientists could use the best methods and ideas in their academic research, without fear of litigation.

HARVMegaphone2 GROUPED.png

For more information on Harvard iGEM's Human Practices activism,

References

1. Mankiw, G. (2012). Principles of Economics. New York: South-Western Cengage Learning.

2. Chandrasekharan, S., Kumar, S., Valley, C., & Rai, A. (2009). Proprietary science, open science and the role of patent disclosure: the case of zinc-finger proteins. Nature Biotechnology, 140-144. [1]

3. Gorman, R. (2010, Fall). Zinc Fingers: Entry Fee. Proto: Massachusetts General Hospital, Dispatches from the Frontiers of Medicine, pp. 35-39. [2]

4. Jeffry D Sander, Elizabeth J Dahlborg, Mathew J Goodwin, Lindsay Cade, Feng Zhang, Daniel Cifuentes, Shaun J Curtin, Jessica S Blackburn, Stacey Thibodeau-Beganny, Yiping Qi, Christopher J Pierick, Ellen Hoffman, Morgan L Maeder, Cyd Khayter, Deepak Reyon, Drena Dobbs, David M Langenau, Robert M Stupar, Antonio J Giraldez, Daniel F Voytas, Randall T Peterson,Jing-Ruey J Yeh, J Keith Joung. Selection-free zinc-finger-nuclease engineering by context-dependent assembly (CoDA)(2011). Nature Methods 8, 67–69. [3]

5. Morgan L. Maeder, Stacey Thibodeau-Beganny, Anna Osiak, David A. Wright, Reshma M. Anthony, Magdalena Eichtinger, Tao Jiang, Jonathan E. Foley, Ronnie J. Winfrey, Jeffrey A. Townsend, Erica Unger-Wallace, Jeffry D. Sander, Felix Müller-Lerch, Fengli Fu, Joseph Pearlberg, Carl Göbel, Justin P. Dassie, Shondra M. Pruett-Miller, Matthew H. Porteus, Dennis C. Sgroi, A. John Iafrate, Drena Dobbs, Paul B. McCray Jr., Toni Cathomen, Daniel F. Voytas, J. Keith Joung. Rapid “Open-Source” Engineering of Customized Zinc-Finger Nucleases for Highly Efficient Gene Modification (2008). Molecular Cell Volume 31, Issue 2, 25 July 2008, Pages 294-301.[4]

6. Christopher Thomas Scott. The zinc finger nuclease monopoly. Nature Biotechnology Vol23 Num8, 2005.[5]

7. UK Intellectual Property Office. The Patent Research Exception: A Consultation. 2008.[6]

8. Luke Timmerman. Sangamo Fails Diabetic Neuropathy Study, Falls Back on HIV, Other Programs. Xconomy, 10/3/11. [7]