2c8q

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /> <applet load="2c8q" size="450" color="white" frame="true" align="right" spinBox="true" caption="2c8q, resolution 1.95&Aring;" /> '''INSULINE(1SEC) AND ...)
Line 1: Line 1:
-
[[Image:2c8q.gif|left|200px]]<br />
+
[[Image:2c8q.gif|left|200px]]<br /><applet load="2c8q" size="350" color="white" frame="true" align="right" spinBox="true"
-
<applet load="2c8q" size="450" color="white" frame="true" align="right" spinBox="true"
+
caption="2c8q, resolution 1.95&Aring;" />
caption="2c8q, resolution 1.95&Aring;" />
'''INSULINE(1SEC) AND UV LASER EXCITED FLUORESCENCE'''<br />
'''INSULINE(1SEC) AND UV LASER EXCITED FLUORESCENCE'''<br />
==Overview==
==Overview==
-
Structural proteomics has promoted the rapid development of automated, protein structure determination using X-ray crystallography. Robotics are, now routinely used along the pipeline from genes to protein structures., However, a bottleneck still remains. At synchrotron beamlines, the success, rate of automated sample alignment along the X-ray beam is limited by, difficulties in visualization of protein crystals, especially when they, are small and embedded in mother liquor. Despite considerable improvement, in optical microscopes, the use of visible light transmitted or reflected, by the sample may result in poor or misleading contrast. Here, the, endogenous fluorescence from aromatic amino acids has been used to, identify even tiny or weakly fluorescent crystals with a high success, rate. The use of a compact laser at 266 nm in combination with, non-fluorescent sample holders provides an efficient solution to collect, high-contrast fluorescence images in a few milliseconds and using standard, camera optics. The best image quality was obtained with direct, illumination through a viewing system coaxial with the UV beam., Crystallographic data suggest that the employed UV exposures do not, generate detectable structural damage.
+
Structural proteomics has promoted the rapid development of automated protein structure determination using X-ray crystallography. Robotics are now routinely used along the pipeline from genes to protein structures. However, a bottleneck still remains. At synchrotron beamlines, the success rate of automated sample alignment along the X-ray beam is limited by difficulties in visualization of protein crystals, especially when they are small and embedded in mother liquor. Despite considerable improvement in optical microscopes, the use of visible light transmitted or reflected by the sample may result in poor or misleading contrast. Here, the endogenous fluorescence from aromatic amino acids has been used to identify even tiny or weakly fluorescent crystals with a high success rate. The use of a compact laser at 266 nm in combination with non-fluorescent sample holders provides an efficient solution to collect high-contrast fluorescence images in a few milliseconds and using standard camera optics. The best image quality was obtained with direct illumination through a viewing system coaxial with the UV beam. Crystallographic data suggest that the employed UV exposures do not generate detectable structural damage.
==Disease==
==Disease==
Line 11: Line 10:
==About this Structure==
==About this Structure==
-
2C8Q is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2C8Q OCA].
+
2C8Q is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2C8Q OCA].
==Reference==
==Reference==
Line 33: Line 32:
[[Category: uv]]
[[Category: uv]]
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 21:12:35 2007''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:46:06 2008''

Revision as of 14:46, 21 February 2008


2c8q, resolution 1.95Å

Drag the structure with the mouse to rotate

INSULINE(1SEC) AND UV LASER EXCITED FLUORESCENCE

Contents

Overview

Structural proteomics has promoted the rapid development of automated protein structure determination using X-ray crystallography. Robotics are now routinely used along the pipeline from genes to protein structures. However, a bottleneck still remains. At synchrotron beamlines, the success rate of automated sample alignment along the X-ray beam is limited by difficulties in visualization of protein crystals, especially when they are small and embedded in mother liquor. Despite considerable improvement in optical microscopes, the use of visible light transmitted or reflected by the sample may result in poor or misleading contrast. Here, the endogenous fluorescence from aromatic amino acids has been used to identify even tiny or weakly fluorescent crystals with a high success rate. The use of a compact laser at 266 nm in combination with non-fluorescent sample holders provides an efficient solution to collect high-contrast fluorescence images in a few milliseconds and using standard camera optics. The best image quality was obtained with direct illumination through a viewing system coaxial with the UV beam. Crystallographic data suggest that the employed UV exposures do not generate detectable structural damage.

Disease

Known diseases associated with this structure: Diabetes mellitus, rare form OMIM:[176730], Hyperproinsulinemia, familial OMIM:[176730], MODY, one form OMIM:[176730]

About this Structure

2C8Q is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

UV laser-excited fluorescence as a tool for the visualization of protein crystals mounted in loops., Vernede X, Lavault B, Ohana J, Nurizzo D, Joly J, Jacquamet L, Felisaz F, Cipriani F, Bourgeois D, Acta Crystallogr D Biol Crystallogr. 2006 Mar;62(Pt 3):253-61. Epub 2006, Feb 22. PMID:16510972

Page seeded by OCA on Thu Feb 21 16:46:06 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools