2q57

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(New page: 200px<br /><applet load="2q57" size="350" color="white" frame="true" align="right" spinBox="true" caption="2q57, resolution 2.00&Aring;" /> '''X-ray structure of C...)
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[[Image:2q57.jpg|left|200px]]<br /><applet load="2q57" size="350" color="white" frame="true" align="right" spinBox="true"
 
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caption="2q57, resolution 2.00&Aring;" />
 
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'''X-ray structure of Cerulean GFP: A tryptophan-based chromophore useful for fluorescence lifetime imaging'''<br />
 
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==Overview==
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==X-ray structure of Cerulean GFP: A tryptophan-based chromophore useful for fluorescence lifetime imaging==
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The crystal structure of the cyan-fluorescent Cerulean green fluorescent, protein (GFP), a variant of enhanced cyan fluorescent protein (ECFP), has, been determined to 2.0 A. Cerulean bears an internal fluorophore composed, of an indole moiety derived from Y66W, conjugated to the GFP-like, imidazolinone ring via a methylene bridge. Cerulean undergoes highly, efficient fluorescence resonance energy transfer (FRET) to yellow acceptor, molecules and exhibits significantly reduced excited-state heterogeneity., This feature was rationally engineered in ECFP by substituting His148 with, an aspartic acid [Rizzo et al. (2004) Nat. Biotechnol. 22, 445], rendering, Cerulean useful for fluorescence lifetime imaging microscopy (FLIM). The, X-ray structure is consistent with a single conformation of the, chromophore and surrounding residues and may therefore provide a, structural rationale for the previously described monoexponential, fluorescence decay. Unexpectedly, the carboxyl group of H148D is found in, a buried position, directly contacting the indole nitrogen of the, chromophore via a bifurcated hydrogen bond. Compared to the similarly, constructed ECFP chromophore, the indole group of Cerulean is rotated, around the methylene bridge to adopt a cis-coplanar conformation with, respect to the imidazolinone ring, resulting in a close edge-to-edge, contact of the two ring systems. The double-humped absorbance spectrum, persists in single-crystal absorbance measurements, casting doubt on the, idea that ground state conformational heterogeneity forms the basis of the, two overlapping transitions. At low pH, a blue shift in absorbance of, 10-15 nm suggests a pH-induced structural transition that proceeds with a, time constant of 47 (+/-2) min and is reversible. Possible interpretations, in terms of chromophore isomerization are presented.
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<StructureSection load='2q57' size='340' side='right'caption='[[2q57]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[2q57]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Aequorea_victoria Aequorea victoria]. The June 2014 RCSB PDB [https://pdb.rcsb.org/pdb/static.do?p=education_discussion/molecule_of_the_month/index.html Molecule of the Month] feature on ''GFP-like Proteins'' by David Goodsell is [https://dx.doi.org/10.2210/rcsb_pdb/mom_2014_6 10.2210/rcsb_pdb/mom_2014_6]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2Q57 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2Q57 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CRF:[(4Z)-2-[(1R,2R)-1-AMINO-2-HYDROXYPROPYL]-4-(1H-INDOL-3-YLMETHYLIDENE)-5-OXO-4,5-DIHYDRO-1H-IMIDAZOL-1-YL]ACETIC+ACID'>CRF</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2q57 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2q57 OCA], [https://pdbe.org/2q57 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2q57 RCSB], [https://www.ebi.ac.uk/pdbsum/2q57 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2q57 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/GFP_AEQVI GFP_AEQVI] Energy-transfer acceptor. Its role is to transduce the blue chemiluminescence of the protein aequorin into green fluorescent light by energy transfer. Fluoresces in vivo upon receiving energy from the Ca(2+)-activated photoprotein aequorin.
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== Evolutionary Conservation ==
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[[Image:Consurf_key_small.gif|200px|right]]
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Check<jmol>
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<jmolCheckbox>
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<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/q5/2q57_consurf.spt"</scriptWhenChecked>
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<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview03.spt</scriptWhenUnchecked>
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<text>to colour the structure by Evolutionary Conservation</text>
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</jmolCheckbox>
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</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=2q57 ConSurf].
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<div style="clear:both"></div>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The crystal structure of the cyan-fluorescent Cerulean green fluorescent protein (GFP), a variant of enhanced cyan fluorescent protein (ECFP), has been determined to 2.0 A. Cerulean bears an internal fluorophore composed of an indole moiety derived from Y66W, conjugated to the GFP-like imidazolinone ring via a methylene bridge. Cerulean undergoes highly efficient fluorescence resonance energy transfer (FRET) to yellow acceptor molecules and exhibits significantly reduced excited-state heterogeneity. This feature was rationally engineered in ECFP by substituting His148 with an aspartic acid [Rizzo et al. (2004) Nat. Biotechnol. 22, 445], rendering Cerulean useful for fluorescence lifetime imaging microscopy (FLIM). The X-ray structure is consistent with a single conformation of the chromophore and surrounding residues and may therefore provide a structural rationale for the previously described monoexponential fluorescence decay. Unexpectedly, the carboxyl group of H148D is found in a buried position, directly contacting the indole nitrogen of the chromophore via a bifurcated hydrogen bond. Compared to the similarly constructed ECFP chromophore, the indole group of Cerulean is rotated around the methylene bridge to adopt a cis-coplanar conformation with respect to the imidazolinone ring, resulting in a close edge-to-edge contact of the two ring systems. The double-humped absorbance spectrum persists in single-crystal absorbance measurements, casting doubt on the idea that ground state conformational heterogeneity forms the basis of the two overlapping transitions. At low pH, a blue shift in absorbance of 10-15 nm suggests a pH-induced structural transition that proceeds with a time constant of 47 (+/-2) min and is reversible. Possible interpretations in terms of chromophore isomerization are presented.
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==About this Structure==
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X-ray structure of Cerulean GFP: a tryptophan-based chromophore useful for fluorescence lifetime imaging.,Malo GD, Pouwels LJ, Wang M, Weichsel A, Montfort WR, Rizzo MA, Piston DW, Wachter RM Biochemistry. 2007 Sep 4;46(35):9865-73. Epub 2007 Aug 8. PMID:17685554<ref>PMID:17685554</ref>
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2Q57 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Aequorea_victoria Aequorea victoria]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2Q57 OCA].
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==Reference==
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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X-ray structure of Cerulean GFP: a tryptophan-based chromophore useful for fluorescence lifetime imaging., Malo GD, Pouwels LJ, Wang M, Weichsel A, Montfort WR, Rizzo MA, Piston DW, Wachter RM, Biochemistry. 2007 Sep 4;46(35):9865-73. Epub 2007 Aug 8. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=17685554 17685554]
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</div>
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[[Category: Aequorea victoria]]
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<div class="pdbe-citations 2q57" style="background-color:#fffaf0;"></div>
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[[Category: Single protein]]
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[[Category: Malo, G.D.]]
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[[Category: beta barrel]]
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[[Category: fluorescent protein]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 11:59:08 2008''
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==See Also==
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*[[Green Fluorescent Protein 3D structures|Green Fluorescent Protein 3D structures]]
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Aequorea victoria]]
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[[Category: GFP-like Proteins]]
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[[Category: Large Structures]]
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[[Category: RCSB PDB Molecule of the Month]]
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[[Category: Malo GD]]

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X-ray structure of Cerulean GFP: A tryptophan-based chromophore useful for fluorescence lifetime imaging

PDB ID 2q57

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