Team:Cambridge/Project

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Bact<b>iridescence</b> was based around the properties of [[Team:Cambridge/Project/Background | reflectin]], a squid protein with the highest refractive index of any known proteinaceous substance. In squid this protein forms complex platelets which act as [http://en.wikipedia.org/wiki/Bragg_reflector Bragg reflectors] to provide camouflage.
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===Project Goals===
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''Bact'''iridescence''''' is a project based around the unique properties of reflectin, a squid protein with the highest refractive index of any known proteinaceous substance.  In squid this protein forms complex platelets which act as [http://en.wikipedia.org/wiki/Distributed_Bragg_reflector Bragg reflectors] to provide camouflage. We aim to express reflectin in E. coli and optimise the optical properties in order to build the groundwork for the manipulation of living structural colour.
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We aimed to [[Team:Cambridge/Project/In_Vivo | express reflectin in ''E. coli'']] and to investigate its optical properties in order to build the groundwork for the manipulation of living structural colour. We also looked at the [[Team:Cambridge/Project/In_Vitro | over-expression of reflectin in ''E. coli'']], in order to obtain relatively pure samples of the protein for making thin films.
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=Background to our project=
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Much of our work (particularly the in vivo work) simply hadn't been tried before, so, while we had high hopes, we could not be sure as to what would happen.
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==How to Disappear Completely - Reflectins in cephalopods==
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==Achievements==
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In one short summer the [[Team:Cambridge/Team | 2011 Cambridge team]] has produced a set of [[Team:Cambridge/Parts | BioBrick parts]] to allow future researchers to explore synthetic biology applications for structural colour.
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The beautiful optical properties which reflectins make possible are used for a multitude of purposed within nature. Manipulation of reflectance allows squids to communicate through polarised light whilst altering the refractive index to match that of the water column allows cephalopods to hide from their predators, the very replication of a living invisibility cloak.  
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===[[Team:Cambridge/Project/In_Vivo | In Vivo]]===
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Working with living cells we have;
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*[[Team:Cambridge/Project/Microscopy | Imaged squid tissue using novel techniques]] to explore the in vivo properties of reflectins.
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*Succesfully produced reflectins in ''E. coli''.
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*Characterised best practices for in vivo reflectin production.
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Reflectin was first identified as such in the Hawaiian bobtail squid [http://en.wikipedia.org/wiki/Euprymna_scolopes ''Euprymna scolopes''] as the protein responsible for a reflective layer in the "light organ". This layer reflects light emitted by symbiotic bacteria to be reflected downwards away from the squid for camouflage, like a [http://en.wikipedia.org/wiki/Headlamp#Reflector_lamps car headlamp].
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===[[Team:Cambridge/Project/In_Vitro | In Vitro]]===
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[[File:Cam_Multilayer_drop_1.jpg | right | thumb | 150px | A multilayer thin film]]
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By engineering ''E. coli'' to overexpress reflectins we have;
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*[[Team:Cambridge/Experiments/Protein_Purification | Purified reflectin]] and documented best practice for high purity yields.
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*Made [[Team:Cambridge/Project/Microscopy#Reflectin_Thin_Films | thin films]] which show structural colours.
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*Demonstrated the rapid colour changes possible with reflectin.
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**Videos of our thin films are available on [http://www.youtube.com/user/cambridgeigem2011 youtube].
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Whereas the effect is static in E.scolopes, the Longfin inshore squid [http://en.wikipedia.org/wiki/Longfin_Inshore_Squid ''Loligo pealei''] demonstrates dynamic iridescence which are controlled by the nervous system<sup>[[#Izumi|[5]]]</sup>. The neural-signals switches a [http://en.wikipedia.org/wiki/Kinase protein kinase], an enzyme which adds negatively charged phosphate groups to the positively charged protein. Within the squid reflectin is structured hierarchially, the structure of the reflectin protein itself, the complex platelets which form and the final multi-layer 'Bragg stack' of platelets contained within reflective cells called iridophores<sup>[[#Morse|[3]]]</sup>. The negatively charged phosphate groups alters the spacing between the protein layers and therefore the colour by changing the attraction/repulsion between the reflectin platelets.(Read more about structural colour)
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===[[Team:Cambridge/Project/Gibthon | Software]]===
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[[File:Gibthon2.0beta.png | left | thumb | 100px | The Gibthon logo]]
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We contributed to [http://www.gibthon.org/ Gibthon], an open-source collection of web-based tools for construct design, fully compatible with both BioBrick standards and newer assembly techniques.
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*Greatly improved import and display of fragments (including support for [http://partsregistry.org/Main_Page partsregistry.org]).
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*Added tools to allow management of uploaded parts.
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<center>
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<html><div style='clear:both'></div></html>
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<gallery>
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File:CAM_LOLIGO_IRIDOCYTES.jpg | EM of reflectin ultrastructure (dark bands) in cells from ''Loligo opalescens''<sup>[[#Octopus|[6]]]</sup>
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File:CAM_OCTOPUS_IRIDOCYTES.jpg | EM of reflectin ultrastructure (dark bands) in reflector cells from ''Octopus dofleini''<sup>[[#Octopus|[6]]]</sup>
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File:CAM_CLAM.jpg | Structural colour in the mantle of a giant clam creates beautiful blue-green hues
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</gallery>
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</center>
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Iridophores are not merely confined in cephalopods but can also be found in other members of mollusc phylum e.g. giant clams<sup>[[#Clams|[4]]]</sup>where they are responsible for the stunning iridescent colours of the mantle, and they may play a role in protecting against harmful UV and maximising capture of sunlight for the photosynthetic symbionts.
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==[[Team:Cambridge/Project/Future | Future work]]==
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==Light and interference - The physics behind structural colour==
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By creating the first BioBrick parts for production of structural colour, we hope to facilitate further research. Although time did not allow us to explore the full potential of our project, we have some ideas for what could be done next.
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[[File:Cam_ThinFilmInterference.jpg | thumb | Diagram showing how light reflects from a thin film]]
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Structural colour is a common occurrence in nature - butterfly wings, fish scales and even [http://en.wikipedia.org/wiki/Tapetum_lucidum cats's eyes] contain light reflecting components rather than pigments. It occurs due to the phenomenon of [http://en.wikipedia.org/wiki/Thin-film_interference '''thin film interference'''].
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The difference in [http://en.wikipedia.org/wiki/Refractive_index refractive index] between the alternating layers leads to reflection (bouncing off) and transmission of light. This process is repeated at each layer. When the two reflected light waves meet, they sum together but are no longer in sync (due to differences in the optical paths they have taken) leading to the phenomenon known as interference. [[File:Cam-2D_interference.png | thumb | Examples of 2D interference patterns]] Some wavelengths will destructively interfere more than others. The result is that not all colours are reflected with the same intensity, creating rainbow-like effects like those of oil droplets on the surface of water or the surface of shimmering soap bubbles.
 
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The observed colour changes with viewing angle, angle of incidence of light and alterations in the spacing of the layers or refractive indices which alters the mechanism of interference. In fact, if you use layers of materials with matching refractive indices, total transparency and hence invisibility of the material can be achieved.
 
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This principle of interference is believed to be the primary mechanism by which colour is controlled in the skin of squid. Experimental observations of changes in the thickness and spacing between reflectin layers ''in-vivo'' has been observed following post translational modification.
 
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==Reflectins as Novel Polymers==
 
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Reflectins unique properties partly stem from their unique amino acid composition; residues normally common in proteins (alanine, isoleucine, leucine and lysine) are nowhere to be found in any reflectins identified thus far. Meanwhile typically rare residues (arginine, methionine, tryptophan and tyrosine) make up almost 57% of the protein! The family of reflectin proteins also share a repeated domain which could also possess some unique optical characteristics.
 
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[[File:Cam-beta_barrel.png | thumb |A typical example of a beta-barrel structure]]
 
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The 3D protein structure of reflectin has not yet been documented.  It may be natively unstructured, Weiss ''et al'' hypothesised that it may form a [http://en.wikipedia.org/wiki/Beta_barrel beta barrel] like structure when interacting with membranes, as recombinant reflectin-like proteins associates strongly with artificial membrane structures after cell-free expression.
 
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Kramer ''et al'' and Tao and DeMartini ''et al'' have demonstrated the remarkable capability of reflectin proteins to self assemble in vitro to create complex structures.  Recombinant reflectin, refolded ''in vitro'', can be carefully spread along a silicon slide to make thin films with intense structural colours which showed iridescence. Measurement of the refractive index revealed reflectin possessing the highest refractive index of any natural known protein. In addition Kramer ''et al'' demonstrated the ability of reflectin to form a diffraction grating when ionic solvents used to dissolve it, were diffused away in a water bath. 
 
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[[File:CAM_THIN_FILM.jpg | thumb | Thin films cast from different concentrations of reflectin<sup>[[#Kramer|[1]]]</sup>]]
 
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=Objective One - Express reflectin in E. coli=
 
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Our first objective was to try to express reflectin, in any shape or form, in E. coli. Ideally, we'd be able to express reflectin in the bacteria at a range of levels using a single construct, so we can both overexpress (for ''in vitro'' studies) or underexpress (to promote ''in vivo'' folding) straightforwardly. In order to do this, we had to create an expression plasmid for reflectin with which we could transform the bacterial cells. Hence, we had to isolate a reflectin gene sequence, choose a suitable promotor and join them on an appropriate backbone in order to engineer what we wanted. These steps are outlined below.
 
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[[File:camflow_1.jpg | 600px | Objective One]]
 
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==Isolating the reflectin gene==
 
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This was
 
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==Selecting the promotor==
 
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==Selecting the backbone==
 
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==Creating the expression plasmid==
 
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Hopefully coming soon!
 
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==Expression in E. coli==
 
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Hopefully coming soon!
 
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=='''References'''==
 
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<div id="Kramer"></div>[http://www.nature.com/nmat/journal/v6/n7/abs/nmat1930.html] Kramer ''et al.'' '''The self-organizing properties of squid reflectin protein''' Nature Materials 533-538 VOL6 JULY 2007
 
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<div id="Crookes"></div>[http://www.sciencemag.org/content/303/5655/235.short] Crookes ''et al.'' '''Reflectins: The Unusual Proteins of Squid Reflective Tissues''' SCIENCE 235-238 VOL303 9 JANUARY 2004
 
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<div id="Morse"></div>[http://www.sciencedirect.com/science/article/pii/S0142961209011442] Morse ''et al.'' '''The role of protein assembly in dynamically tunable bio-optical tissues''' Biomaterials 793-801 VOL31 FEBRUARY 2010
 
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<div id="Clams"></div>[http://www.publish.csiro.au/paper/ZO9920319.html] Griffiths ''et al''. '''Iridophores in the mantle of giant clams.''' Australian Journal of Zoology (1992) Volume: 40, Issue: 3 Pages: 319-326
 
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<div id="Izumi"></div>[http://www.ncbi.nlm.nih.gov/pubmed/19776150] Izumi ''et al''. '''Changes in reflectin protein phosphorylation are associated with dynamic iridescence in squid.''' J. R. Soc. Interface 6 March 2010 vol. 7 no. 44 549-560
 
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<div id="Octopus"></div>[http://www.springerlink.com/content/bba14b73ad35f495/]Brocco ''et al''. '''Reflector cells in the skin of ''Octopus dofleini''''' Cell and Tissue Research, Volume 205, Number 2, 167-186, 1980
 
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Latest revision as of 02:52, 22 September 2011

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OVERVIEW
home
Bactiridescence was based around the properties of reflectin, a squid protein with the highest refractive index of any known proteinaceous substance. In squid this protein forms complex platelets which act as [http://en.wikipedia.org/wiki/Bragg_reflector Bragg reflectors] to provide camouflage.

Contents

Project Goals

We aimed to express reflectin in E. coli and to investigate its optical properties in order to build the groundwork for the manipulation of living structural colour. We also looked at the over-expression of reflectin in E. coli, in order to obtain relatively pure samples of the protein for making thin films.

Much of our work (particularly the in vivo work) simply hadn't been tried before, so, while we had high hopes, we could not be sure as to what would happen.

Achievements

In one short summer the 2011 Cambridge team has produced a set of BioBrick parts to allow future researchers to explore synthetic biology applications for structural colour.

In Vivo

Working with living cells we have;

In Vitro

A multilayer thin film

By engineering E. coli to overexpress reflectins we have;

  • Purified reflectin and documented best practice for high purity yields.
  • Made thin films which show structural colours.
  • Demonstrated the rapid colour changes possible with reflectin.
    • Videos of our thin films are available on [http://www.youtube.com/user/cambridgeigem2011 youtube].

Software

The Gibthon logo

We contributed to [http://www.gibthon.org/ Gibthon], an open-source collection of web-based tools for construct design, fully compatible with both BioBrick standards and newer assembly techniques.

  • Greatly improved import and display of fragments (including support for [http://partsregistry.org/Main_Page partsregistry.org]).
  • Added tools to allow management of uploaded parts.

Future work

By creating the first BioBrick parts for production of structural colour, we hope to facilitate further research. Although time did not allow us to explore the full potential of our project, we have some ideas for what could be done next.