1gzl

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:1gzl.jpg|left|200px]]
+
{{Seed}}
 +
[[Image:1gzl.png|left|200px]]
<!--
<!--
Line 9: Line 10:
{{STRUCTURE_1gzl| PDB=1gzl | SCENE= }}
{{STRUCTURE_1gzl| PDB=1gzl | SCENE= }}
-
'''CRYSTAL STRUCTURE OF C14LINKMID/IQN17: A CROSS-LINKED INHIBITOR OF HIV-1 ENTRY BOUND TO THE GP41 HYDROPHOBIC POCKET'''
+
===CRYSTAL STRUCTURE OF C14LINKMID/IQN17: A CROSS-LINKED INHIBITOR OF HIV-1 ENTRY BOUND TO THE GP41 HYDROPHOBIC POCKET===
-
==Overview==
+
<!--
-
Peptides corresponding to the C-terminal heptad repeat of HIV-1 gp41 (C-peptides) are potent inhibitors of HIV-1 entry into cells. Their mechanism of inhibition involves binding in a helical conformation to the central coiled coil of HIV-1 gp41 in a dominant-negative manner. Short C-peptides, however, have low binding affinity for gp41 and poor inhibitory activity, which creates an obstacle to the development of small drug-like C-peptides. To improve the inhibitory potency of short C-peptides that target the hydrophobic pocket region of gp41, we use two strategies to stabilize the C-peptide helix: chemical crosslinking and substitution with unnatural helix-favoring amino acids. In this study, the short linear peptide shows no significant inhibitory activity, but a constrained peptide (C14linkmid) inhibits cell-cell fusion at micromolar potency. Structural studies confirm that the constrained peptides bind to the gp41 hydrophobic pocket. Calorimetry reveals that, of the peptides analyzed, the most potent are those that best balance the changes in binding enthalpy and entropy, and surprisingly not those with the highest helical propensity as measured by circular dichroism spectroscopy. Our study reveals the thermodynamic basis of inhibition of an HIV C-peptide, demonstrates the utility of constraining methods for a short antiviral peptide inhibitor, and has implications for the future design of constrained peptides.
+
The line below this paragraph, {{ABSTRACT_PUBMED_12417739}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 12417739 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_12417739}}
==About this Structure==
==About this Structure==
Line 31: Line 35:
[[Category: Hiv entry]]
[[Category: Hiv entry]]
[[Category: Inhibitor]]
[[Category: Inhibitor]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 18:13:22 2008''
+
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 1 06:22:31 2008''

Revision as of 03:22, 1 July 2008

Template:STRUCTURE 1gzl

CRYSTAL STRUCTURE OF C14LINKMID/IQN17: A CROSS-LINKED INHIBITOR OF HIV-1 ENTRY BOUND TO THE GP41 HYDROPHOBIC POCKET

Template:ABSTRACT PUBMED 12417739

About this Structure

1GZL is a Single protein structure. Full crystallographic information is available from OCA.

Reference

Short constrained peptides that inhibit HIV-1 entry., Sia SK, Carr PA, Cochran AG, Malashkevich VN, Kim PS, Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):14664-9. Epub 2002 Nov 4. PMID:12417739

Page seeded by OCA on Tue Jul 1 06:22:31 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools