Team:Cambridge/Project/Future
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- | == | + | =Future ideas= |
+ | ==Reflectins as optical materials== | ||
- | == | + | As a proteinaceous substance which self assembles into nanoscale structures, reflectins could be the future of nanophotonic devices. |
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+ | -Flexible substrates - did we have ideas for this? | ||
+ | -Different methods for controlling colour change | ||
+ | -Pixel | ||
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+ | ==Reflectins as novel biosensors== | ||
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+ | Spectrum spanning colour changes in ''Loligo pealeii'' tissue samples [http://rsif.royalsocietypublishing.org/content/7/44/549.long#F2 can occur in a few minutes]. This could provide a real-time response exceeding that of [http://www.plosone.org/article/info:doi%2F10.1371%2Fjournal.pone.0002351 superfast GFP] or previous attempts to create [https://2010.igem.org/Team:Imperial_College_London/Modules/Fast_Response fast pigment production] - a highly attractive feature in a biosensor. | ||
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+ | In ''L. pealeii'' this is thought to be [[Team:Cambridge/Project/Background | controlled by a tyrosine kinase]], so a screen of predicted tyrosine kinases from a squid cDNA library or protein engineering to create kinase recognition sites could recreate this rapid colour change in vivo in responses to changes in a signal cascade. | ||
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+ | =Groundwork needed= | ||
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+ | ==Living structural colour with recombinant reflectins== | ||
As of the time of writing we were unable to produce convincing evidence of a [[Team:Cambridge/Project/Microscopy | change in the optical | As of the time of writing we were unable to produce convincing evidence of a [[Team:Cambridge/Project/Microscopy | change in the optical | ||
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We made the decision to focus on expression in ''E. coli'' due to their short replication time and because our [[Team:Cambridge/Team/Advisors | advisors]] have a great deal of experience working with bacteria. However, reflectin is a eukaryotic protein and may require chaperones or a specialised lipid composition to associate with membranes. In addition, the iridophore platelets in squid cells are considerably longer than a bacterial cell - size constraints may be limiting the assembly process. Synthetic biology is developing toolkits for many eukaryotic systems including [http://partsregistry.org/Yeast yeast] and [[Team:UEA-JIC_Norwich | plant cells]] - these may hold the key for living structural colour. | We made the decision to focus on expression in ''E. coli'' due to their short replication time and because our [[Team:Cambridge/Team/Advisors | advisors]] have a great deal of experience working with bacteria. However, reflectin is a eukaryotic protein and may require chaperones or a specialised lipid composition to associate with membranes. In addition, the iridophore platelets in squid cells are considerably longer than a bacterial cell - size constraints may be limiting the assembly process. Synthetic biology is developing toolkits for many eukaryotic systems including [http://partsregistry.org/Yeast yeast] and [[Team:UEA-JIC_Norwich | plant cells]] - these may hold the key for living structural colour. | ||
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==Further Work== | ==Further Work== |
Revision as of 10:06, 20 September 2011
Contents |
Future ideas
Reflectins as optical materials
As a proteinaceous substance which self assembles into nanoscale structures, reflectins could be the future of nanophotonic devices.
-Flexible substrates - did we have ideas for this? -Different methods for controlling colour change -Pixel
Reflectins as novel biosensors
Spectrum spanning colour changes in Loligo pealeii tissue samples [http://rsif.royalsocietypublishing.org/content/7/44/549.long#F2 can occur in a few minutes]. This could provide a real-time response exceeding that of [http://www.plosone.org/article/info:doi%2F10.1371%2Fjournal.pone.0002351 superfast GFP] or previous attempts to create fast pigment production - a highly attractive feature in a biosensor.
In L. pealeii this is thought to be controlled by a tyrosine kinase, so a screen of predicted tyrosine kinases from a squid cDNA library or protein engineering to create kinase recognition sites could recreate this rapid colour change in vivo in responses to changes in a signal cascade.
Groundwork needed
Living structural colour with recombinant reflectins
As of the time of writing we were unable to produce convincing evidence of a change in the optical properties of E. coli. However, we had a number of ideas to try and promote self-assembly of the reflectin ultrastructure to give thin film interference.
Export to the periplasm
We attempted to export both our reflectin and our reflectin-GFP fusion to the periplasm, in the hope that this environment would be more similar to the environment in which reflectin naturally folds and that the small space will promote reflectin's membrane-associating properties. As of writing we were unable to achieve succesful export, but we hope that this may result in reflectin membrane association.
Expressing multiple reflectins
Squid reflector cells contain more than just one reflectin - for example, [http://www.sciencemag.org/content/303/5655/235.full the original study] in E. scolopes identified at least 6 different genes for reflectins. Little is known about the interactions between these homologues - it may be possible to promote reflectin assembly by expressing a suite of different proteins.
Protein engineering
Rational engineering of reflectins to add membrane-binding domains may give an approximation of native reflectin membrane association.
Eukaryotic cells
We made the decision to focus on expression in E. coli due to their short replication time and because our advisors have a great deal of experience working with bacteria. However, reflectin is a eukaryotic protein and may require chaperones or a specialised lipid composition to associate with membranes. In addition, the iridophore platelets in squid cells are considerably longer than a bacterial cell - size constraints may be limiting the assembly process. Synthetic biology is developing toolkits for many eukaryotic systems including [http://partsregistry.org/Yeast yeast] and plant cells - these may hold the key for living structural colour.
Further Work
No research group has yet induced exogenously-introduced reflectin to give colour in-vivo. It is unlikely that it is folding correctly, whether over-expressed or induced at low levels. Aiding in-vivo folding, e.g. through protein engineering could restore some of the optical effects seen in the squid; it should be borne in mind however that there is excellent evidence that the protein requires an associated membrane complex for its optical function (Tao et al. Biomaterials 5, pp. 793-801).
A number of research groups are interested in developing reflectin as a novel bio-reporter. Within the squid the colour of the protein structure is dynamically altered through phosphorylation on specific residues. If this effect could be recreated in-vivo a coloured reporter could be made to result that continually reports on changes in signal.
The team have demonstrated that thin films of reflectin have interesting in-vitro properties, not least the ability to display colour from across the entire visible spectrum. Should the films be made to change colour reliably in response to e.g. an applied charge, novel displays could be formed without some of the disadvantages of current technology, such as the need for a continual backlight.