1bx3: Difference between revisions

New page: left|200px<br /><applet load="1bx3" size="450" color="white" frame="true" align="right" spinBox="true" caption="1bx3, resolution 2.30Å" /> '''EFFECTS OF COMMONLY ...
 
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caption="1bx3, resolution 2.30&Aring;" />
'''EFFECTS OF COMMONLY USED CRYOPROTECTANTS ON GLYCOGEN PHOSPHORYLASE ACTIVITY AND STRUCTURE'''<br />
'''EFFECTS OF COMMONLY USED CRYOPROTECTANTS ON GLYCOGEN PHOSPHORYLASE ACTIVITY AND STRUCTURE'''<br />


==Overview==
==Overview==
The effects of a number of cryoprotectants on the kinetic and structural, properties of glycogen phosphorylase b have been investigated. Kinetic, studies showed that glycerol, one of the most commonly used, cryoprotectants in X-ray crystallographic studies, is a competitive, inhibitor with respect to substrate glucose-1-P with an apparent Ki value, of 3.8% (v/v). Cryogenic experiments, with the enzyme, have shown that, glycerol binds at the catalytic site and competes with glucose analogues, that bind at the catalytic site, thus preventing the formation of, complexes. This necessitated a change in the conditions for cryoprotection, in crystallographic binding experiments with glycogen phosphorylase. It, was found that 2-methyl-2,4-pentanediol (MPD), polyethylene glycols (PEGs), of various molecular weights, and dimethyl sulfoxide (DMSO) activated, glycogen phosphorylase b to different extents, by stabilizing its most, active conformation, while sucrose acted as a noncompetitive inhibitor and, ethylene glycol as an uncompetitive inhibitor with respect to glucose-1-P., A parallel experimental investigation by X-ray crystallography showed, that, at 100 K, both MPD and DMSO do not bind at the catalytic site, do, not induce any significant conformational change on the enzyme molecule, and hence, are more suitable cryoprotectants than glycerol for binding, studies with glycogen phosphorylase.
The effects of a number of cryoprotectants on the kinetic and structural properties of glycogen phosphorylase b have been investigated. Kinetic studies showed that glycerol, one of the most commonly used cryoprotectants in X-ray crystallographic studies, is a competitive inhibitor with respect to substrate glucose-1-P with an apparent Ki value of 3.8% (v/v). Cryogenic experiments, with the enzyme, have shown that glycerol binds at the catalytic site and competes with glucose analogues that bind at the catalytic site, thus preventing the formation of complexes. This necessitated a change in the conditions for cryoprotection in crystallographic binding experiments with glycogen phosphorylase. It was found that 2-methyl-2,4-pentanediol (MPD), polyethylene glycols (PEGs) of various molecular weights, and dimethyl sulfoxide (DMSO) activated glycogen phosphorylase b to different extents, by stabilizing its most active conformation, while sucrose acted as a noncompetitive inhibitor and ethylene glycol as an uncompetitive inhibitor with respect to glucose-1-P. A parallel experimental investigation by X-ray crystallography showed that, at 100 K, both MPD and DMSO do not bind at the catalytic site, do not induce any significant conformational change on the enzyme molecule, and hence, are more suitable cryoprotectants than glycerol for binding studies with glycogen phosphorylase.


==About this Structure==
==About this Structure==
1BX3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Oryctolagus_cuniculus Oryctolagus cuniculus] with PLP as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Phosphorylase Phosphorylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.1.1 2.4.1.1] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1BX3 OCA].  
1BX3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Oryctolagus_cuniculus Oryctolagus cuniculus] with <scene name='pdbligand=PLP:'>PLP</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Phosphorylase Phosphorylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.1.1 2.4.1.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1BX3 OCA].  


==Reference==
==Reference==
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[[Category: Phosphorylase]]
[[Category: Phosphorylase]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Fleet, G.W.J.]]
[[Category: Fleet, G W.J.]]
[[Category: Gregoriou, M.]]
[[Category: Gregoriou, M.]]
[[Category: Johnson, L.N.]]
[[Category: Johnson, L N.]]
[[Category: Oikonomakos, N.G.]]
[[Category: Oikonomakos, N G.]]
[[Category: Skamnaki, V.T.]]
[[Category: Skamnaki, V T.]]
[[Category: Tsitsanou, K.E.]]
[[Category: Tsitsanou, K E.]]
[[Category: Watson, K.A.]]
[[Category: Watson, K A.]]
[[Category: Zographos, S.E.]]
[[Category: Zographos, S E.]]
[[Category: PLP]]
[[Category: PLP]]
[[Category: binding]]
[[Category: binding]]
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[[Category: phosphorylase]]
[[Category: phosphorylase]]


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