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| + | ==Reflectins in Cephalopods <br/><i style='margin-left:25px;font-size:70%;'>or</i><br/> How to Disappear Completely== | ||
| - | + | Reflectins are a family of proteins which self assemble into a multilayered structure in association with membranes. This multilayer interacts with light to give colours in cephalopods due to [[#Interference | thin film interference.]] | |
| - | + | The beautiful optical properties which reflectins make possible are used for a multitude of purposes within nature. Manipulation of reflectance allows squids to communicate through polarised light whilst altering the refractive index of their skin to match that of the water column allows cephalopods to hide from their predators, a living invisibility cloak. | |
| + | 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]. By controlling the light emitted from the light organ, Hawaiian bobtail squid reduce their shadow against the brighter sky, concealing them from predators below. | ||
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| - | + | Whilst the iridescent effect is static in ''E.scolopes'', the Longfin inshore squid [http://en.wikipedia.org/wiki/Longfin_Inshore_Squid ''Loligo pealei''] demonstrates dynamic iridescence, controlled by the nervous system<sup>[[#Izumi|[5]]]</sup>. Dynamic iridescence is controlled by the release of the neurotransmitter acetylcholine. Acetylcholine detection by reflectin containing cells is believed to activate 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 then the final multi-layer 'Bragg stack' of platelets which is contained within reflective cells called iridophores<sup>[[#Morse|[3]]]</sup>. The negatively charged phosphate groups alters the spacing between the protein layers and therefore modifies the colour by changing the attraction/repulsion between the reflectin platelets.(Read more about structural colour below.) | |
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| - | Iridophores are not merely confined | + | Iridophores are not merely confined to cephalopods but are suspected to be present in other members of the 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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=Light and interference - The physics behind structural colour= | =Light and interference - The physics behind structural colour= | ||
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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. | 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. | ||
| - | =Reflectins as Novel | + | =Reflectins as Novel Proteins= |
| - | Reflectins unique properties partly stem from their unique amino acid composition | + | 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. |
[[File:Cam-beta_barrel.png | thumb |A typical example of a beta-barrel structure]] | [[File:Cam-beta_barrel.png | thumb |A typical example of a beta-barrel structure]] | ||
| - | 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 | + | 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 associate strongly with artificial membrane structures after cell-free expression. |
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. | 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. | ||
Latest revision as of 10:47, 21 September 2011
Contents |
Reflectins in Cephalopods
or
How to Disappear Completely
Reflectins are a family of proteins which self assemble into a multilayered structure in association with membranes. This multilayer interacts with light to give colours in cephalopods due to thin film interference.
The beautiful optical properties which reflectins make possible are used for a multitude of purposes within nature. Manipulation of reflectance allows squids to communicate through polarised light whilst altering the refractive index of their skin to match that of the water column allows cephalopods to hide from their predators, a living invisibility cloak.
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]. By controlling the light emitted from the light organ, Hawaiian bobtail squid reduce their shadow against the brighter sky, concealing them from predators below.
Whilst the iridescent effect is static in E.scolopes, the Longfin inshore squid [http://en.wikipedia.org/wiki/Longfin_Inshore_Squid Loligo pealei] demonstrates dynamic iridescence, controlled by the nervous system[5]. Dynamic iridescence is controlled by the release of the neurotransmitter acetylcholine. Acetylcholine detection by reflectin containing cells is believed to activate 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 then the final multi-layer 'Bragg stack' of platelets which is contained within reflective cells called iridophores[3]. The negatively charged phosphate groups alters the spacing between the protein layers and therefore modifies the colour by changing the attraction/repulsion between the reflectin platelets.(Read more about structural colour below.)
 EM of reflectin ultrastructure (dark bands) in cells from Loligo opalescens[6] |
 EM of reflectin ultrastructure (dark bands) in reflector cells from Octopus dofleini[6] |
 Structural colour in the mantle of a giant clam creates beautiful blue-green hues |
Iridophores are not merely confined to cephalopods but are suspected to be present in other members of the mollusc phylum e.g. giant clams[4]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.
Light and interference - The physics behind structural colour
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].
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.
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.
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.
Reflectins as Novel Proteins
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.
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 associate strongly with artificial membrane structures after cell-free expression.
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.
References
[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 [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 [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 [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 [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 [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
