6pfs: Difference between revisions
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<StructureSection load='6pfs' size='340' side='right'caption='[[6pfs]], [[Resolution|resolution]] 1.76Å' scene=''> | <StructureSection load='6pfs' size='340' side='right'caption='[[6pfs]], [[Resolution|resolution]] 1.76Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[6pfs]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6PFS OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6PFS FirstGlance]. <br> | <table><tr><td colspan='2'>[[6pfs]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Aeqvi Aeqvi]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6PFS OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6PFS FirstGlance]. <br> | ||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | ||
<tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=OHD:'>OHD</scene></td></tr> | <tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=OHD:'>OHD</scene></td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6pfs FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6pfs OCA], [http://pdbe.org/6pfs PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6pfs RCSB], [http://www.ebi.ac.uk/pdbsum/6pfs PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6pfs ProSAT]</span></td></tr> | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6pfs FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6pfs OCA], [http://pdbe.org/6pfs PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6pfs RCSB], [http://www.ebi.ac.uk/pdbsum/6pfs PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6pfs ProSAT]</span></td></tr> | ||
</table> | </table> | ||
<div style="background-color:#fffaf0;"> | |||
== Publication Abstract from PubMed == | |||
Double-bond photoisomerization in molecules such as the green fluorescent protein (GFP) chromophore can occur either via a volume-demanding one-bond-flip pathway or via a volume-conserving hula-twist pathway. Understanding the factors that determine the pathway of photoisomerization would inform the rational design of photoswitchable GFPs as improved tools for super-resolution microscopy. In this communication, we reveal the photoisomerization pathway of a photoswitchable GFP, rsEGFP2, by solving crystal structures of cis and trans rsEGFP2 containing a monochlorinated chromophore. The position of the chlorine substituent in the trans state breaks the symmetry of the phenolate ring of the chromophore and allows us to distinguish the two pathways. Surprisingly, we find that the pathway depends on the arrangement of protein monomers within the crystal lattice: in a looser packing, the one-bond-flip occurs, whereas, in a tighter packing (7% smaller unit cell size), the hula-twist occurs. | |||
Structural Evidence of Photoisomerization Pathways in Fluorescent Proteins.,Chang J, Romei MG, Boxer SG J Am Chem Soc. 2019 Oct 2;141(39):15504-15508. doi: 10.1021/jacs.9b08356. Epub, 2019 Sep 24. PMID:31533429<ref>PMID:31533429</ref> | |||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |||
</div> | |||
<div class="pdbe-citations 6pfs" style="background-color:#fffaf0;"></div> | |||
== References == | |||
<references/> | |||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Aeqvi]] | |||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Boxer, S G]] | [[Category: Boxer, S G]] | ||
Revision as of 10:29, 16 October 2019
rsEGFP2 with a chlorinated chromophore in the fluorescent on-state in a contracted unit cellrsEGFP2 with a chlorinated chromophore in the fluorescent on-state in a contracted unit cell
Structural highlights
Publication Abstract from PubMedDouble-bond photoisomerization in molecules such as the green fluorescent protein (GFP) chromophore can occur either via a volume-demanding one-bond-flip pathway or via a volume-conserving hula-twist pathway. Understanding the factors that determine the pathway of photoisomerization would inform the rational design of photoswitchable GFPs as improved tools for super-resolution microscopy. In this communication, we reveal the photoisomerization pathway of a photoswitchable GFP, rsEGFP2, by solving crystal structures of cis and trans rsEGFP2 containing a monochlorinated chromophore. The position of the chlorine substituent in the trans state breaks the symmetry of the phenolate ring of the chromophore and allows us to distinguish the two pathways. Surprisingly, we find that the pathway depends on the arrangement of protein monomers within the crystal lattice: in a looser packing, the one-bond-flip occurs, whereas, in a tighter packing (7% smaller unit cell size), the hula-twist occurs. Structural Evidence of Photoisomerization Pathways in Fluorescent Proteins.,Chang J, Romei MG, Boxer SG J Am Chem Soc. 2019 Oct 2;141(39):15504-15508. doi: 10.1021/jacs.9b08356. Epub, 2019 Sep 24. PMID:31533429[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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