We apologize for Proteopedia being slow to respond. For the past two years, a new implementation of Proteopedia has been being built. Soon, it will replace this 18-year old system. All existing content will be moved to the new system at a date that will be announced here.

1emg

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:1emg.gif|left|200px]]
+
{{Seed}}
 +
[[Image:1emg.png|left|200px]]
<!--
<!--
Line 9: Line 10:
{{STRUCTURE_1emg| PDB=1emg | SCENE= }}
{{STRUCTURE_1emg| PDB=1emg | SCENE= }}
-
'''GREEN FLUORESCENT PROTEIN (65-67 REPLACED BY CRO, S65T SUBSTITUTION, Q80R)'''
+
===GREEN FLUORESCENT PROTEIN (65-67 REPLACED BY CRO, S65T SUBSTITUTION, Q80R)===
-
==Overview==
+
<!--
-
The green fluorescent protein (GFP) from the jellyfish Aequorea victoria has become a useful tool in molecular and cell biology. Recently, it has been found that the fluorescence spectra of most mutants of GFP respond rapidly and reversibly to pH variations, making them useful as probes of intracellular pH. To explore the structural basis for the titration behavior of the popular GFP S65T variant, we determined high-resolution crystal structures at pH 8.0 and 4.6. The structures revealed changes in the hydrogen bond pattern with the chromophore, suggesting that the pH sensitivity derives from protonation of the chromophore phenolate. Mutations were designed in yellow fluorescent protein (S65G/V68L/S72A/T203Y) to change the solvent accessibility (H148G) and to modify polar groups (H148Q, E222Q) near the chromophore. pH titrations of these variants indicate that the chromophore pKa can be modulated over a broad range from 6 to 8, allowing for pH determination from pH 5 to pH 9. Finally, mutagenesis was used to raise the pKa from 6.0 (S65T) to 7.8 (S65T/H148D). Unlike other variants, S65T/H148D exhibits two pH-dependent excitation peaks for green fluorescence with a clean isosbestic point. This raises the interesting possibility of using fluorescence at this isosbestic point as an internal reference. Practical real time in vivo applications in cell and developmental biology are proposed.
+
The line below this paragraph, {{ABSTRACT_PUBMED_10220315}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 10220315 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_10220315}}
==About this Structure==
==About this Structure==
Line 32: Line 36:
[[Category: Ph titration]]
[[Category: Ph titration]]
[[Category: Photoactive protein]]
[[Category: Photoactive protein]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 15:16:43 2008''
+
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 1 00:59:05 2008''

Revision as of 21:59, 30 June 2008

Image:1emg.png

Template:STRUCTURE 1emg

GREEN FLUORESCENT PROTEIN (65-67 REPLACED BY CRO, S65T SUBSTITUTION, Q80R)

Template:ABSTRACT PUBMED 10220315

About this Structure

1EMG is a Single protein structure of sequence from Aequorea victoria. Full crystallographic information is available from OCA.

Reference

Structural and spectral response of green fluorescent protein variants to changes in pH., Elsliger MA, Wachter RM, Hanson GT, Kallio K, Remington SJ, Biochemistry. 1999 Apr 27;38(17):5296-301. PMID:10220315

Page seeded by OCA on Tue Jul 1 00:59:05 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/1emg"
Personal tools