2ote: Difference between revisions

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[[Image:2ote.jpg|left|200px]]
[[Image:2ote.jpg|left|200px]]


{{Structure
<!--
|PDB= 2ote |SIZE=350|CAPTION= <scene name='initialview01'>2ote</scene>, resolution 1.47&Aring;
The line below this paragraph, containing "STRUCTURE_2ote", creates the "Structure Box" on the page.
|SITE=
You may change the PDB parameter (which sets the PDB file loaded into the applet)  
|LIGAND= <scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene>, <scene name='pdbligand=AYG:[(4E)-2-[(1S)-1-AMINOETHYL]-4-(4-HYDROXYBENZYLIDENE)-5-OXO-4,5-DIHYDRO-1H-IMIDAZOL-1-YL]ACETIC+ACID'>AYG</scene>
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
|ACTIVITY=  
or leave the SCENE parameter empty for the default display.
|GENE= cFP484 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=86521 Clavularia sp.])
-->
|DOMAIN=
{{STRUCTURE_2ote| PDB=2ote  | SCENE= }}  
|RELATEDENTRY=[[2otb|2OTB]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2ote FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ote OCA], [http://www.ebi.ac.uk/pdbsum/2ote PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2ote RCSB]</span>
}}


'''Crystal structure of a monomeric cyan fluorescent protein in the photobleached state'''
'''Crystal structure of a monomeric cyan fluorescent protein in the photobleached state'''
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[[Category: Henderson, J N.]]
[[Category: Henderson, J N.]]
[[Category: Remington, S J.]]
[[Category: Remington, S J.]]
[[Category: beta can]]
[[Category: Beta can]]
[[Category: fluorescent protein]]
[[Category: Fluorescent protein]]
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May  4 11:37:11 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 04:22:49 2008''

Revision as of 08:37, 4 May 2008

File:2ote.jpg

Template:STRUCTURE 2ote

Crystal structure of a monomeric cyan fluorescent protein in the photobleached state


Overview

Fluorescent protein (FP) variants that can be reversibly converted between fluorescent and nonfluorescent states have proven to be a catalyst for innovation in the field of fluorescence microscopy. However, the structural basis of the process remains poorly understood. High-resolution structures of a FP derived from Clavularia in both the fluorescent and the light-induced nonfluorescent states reveal that the rapid and complete loss of fluorescence observed upon illumination with 450-nm light results from cis-trans isomerization of the chromophore. The photoinduced change in configuration from the well ordered cis isomer to the highly nonplanar and disordered trans isomer is accompanied by a dramatic rearrangement of internal side chains. Taken together, the structures provide an explanation for the loss of fluorescence upon illumination, the slow light-independent recovery, and the rapid light-induced recovery of fluorescence. The fundamental mechanism appears to be common to all of the photoactivatable and reversibly photoswitchable FPs reported to date.

About this Structure

2OTE is a Single protein structure of sequence from Clavularia sp.. Full crystallographic information is available from OCA.

Reference

Structural basis for reversible photobleaching of a green fluorescent protein homologue., Henderson JN, Ai HW, Campbell RE, Remington SJ, Proc Natl Acad Sci U S A. 2007 Apr 17;104(16):6672-7. Epub 2007 Apr 9. PMID:17420458 Page seeded by OCA on Sun May 4 11:37:11 2008

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