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New page: left|200px<br /> <applet load="2h3f" size="450" color="white" frame="true" align="right" spinBox="true" caption="2h3f" /> '''Solution structure of the HIV-1 MA protein'...
 
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[[Image:2h3f.gif|left|200px]]<br />
[[Image:2h3f.gif|left|200px]]<br /><applet load="2h3f" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="2h3f" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="2h3f" />
caption="2h3f" />
'''Solution structure of the HIV-1 MA protein'''<br />
'''Solution structure of the HIV-1 MA protein'''<br />


==Overview==
==Overview==
During the late phase of HIV type 1 (HIV-1) replication, newly synthesized, retroviral Gag proteins are targeted to the plasma membrane of most, hematopoietic cell types, where they colocalize at lipid rafts and, assemble into immature virions. Membrane binding is mediated by the matrix, (MA) domain of Gag, a 132-residue polypeptide containing an N-terminal, myristyl group that can adopt sequestered and exposed conformations., Although exposure is known to promote membrane binding, the mechanism by, which Gag is targeted to specific membranes has yet to be established., Recent studies have shown that phosphatidylinositol (PI) 4,5-bisphosphate, [PI(4,5)P(2)], a factor that regulates localization of cellular proteins, to the plasma membrane, also regulates Gag localization and assembly. Here, we show that PI(4,5)P(2) binds directly to HIV-1 MA, inducing a, conformational change that triggers myristate exposure. Related, phosphatidylinositides PI, PI(3)P, PI(4)P, PI(5)P, and PI(3,5)P(2) do not, bind MA with significant affinity or trigger myristate exposure., Structural studies reveal that PI(4,5)P(2) adopts an "extended lipid", conformation, in which the inositol head group and 2'-fatty acid chain, bind to a hydrophobic cleft, and the 1'-fatty acid and exposed myristyl, group bracket a conserved basic surface patch previously implicated in, membrane binding. Our findings indicate that PI(4,5)P(2) acts as both a, trigger of the myristyl switch and a membrane anchor and suggest a, potential mechanism for targeting Gag to membrane rafts.
During the late phase of HIV type 1 (HIV-1) replication, newly synthesized retroviral Gag proteins are targeted to the plasma membrane of most hematopoietic cell types, where they colocalize at lipid rafts and assemble into immature virions. Membrane binding is mediated by the matrix (MA) domain of Gag, a 132-residue polypeptide containing an N-terminal myristyl group that can adopt sequestered and exposed conformations. Although exposure is known to promote membrane binding, the mechanism by which Gag is targeted to specific membranes has yet to be established. Recent studies have shown that phosphatidylinositol (PI) 4,5-bisphosphate [PI(4,5)P(2)], a factor that regulates localization of cellular proteins to the plasma membrane, also regulates Gag localization and assembly. Here we show that PI(4,5)P(2) binds directly to HIV-1 MA, inducing a conformational change that triggers myristate exposure. Related phosphatidylinositides PI, PI(3)P, PI(4)P, PI(5)P, and PI(3,5)P(2) do not bind MA with significant affinity or trigger myristate exposure. Structural studies reveal that PI(4,5)P(2) adopts an "extended lipid" conformation, in which the inositol head group and 2'-fatty acid chain bind to a hydrophobic cleft, and the 1'-fatty acid and exposed myristyl group bracket a conserved basic surface patch previously implicated in membrane binding. Our findings indicate that PI(4,5)P(2) acts as both a trigger of the myristyl switch and a membrane anchor and suggest a potential mechanism for targeting Gag to membrane rafts.


==About this Structure==
==About this Structure==
2H3F is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2H3F OCA].  
2H3F is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2H3F OCA].  


==Reference==
==Reference==
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[[Category: Human immunodeficiency virus 1]]
[[Category: Human immunodeficiency virus 1]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Ghanam, R.H.]]
[[Category: Ghanam, R H.]]
[[Category: Kim, A.]]
[[Category: Kim, A.]]
[[Category: Miller, J.]]
[[Category: Miller, J.]]
[[Category: Saad, J.S.]]
[[Category: Saad, J S.]]
[[Category: Summers, M.F.]]
[[Category: Summers, M F.]]
[[Category: Tai, J.]]
[[Category: Tai, J.]]
[[Category: hiv-1 unmyristoylated ma protein]]
[[Category: hiv-1 unmyristoylated ma protein]]


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