| Literature DB >> 25477243 |
Susanne N Walker1, Rachel L Tennyson, Alex M Chapman, Alan J Kennan, Brian R McNaughton.
Abstract
Methods for the stabilization of well-defined helical peptide drugs and basic research tools have received considerable attention in the last decade. Here, we report the stable and functional display of an HIV gp41 C-peptide helix mimic on a GRAM-Like Ubiquitin-binding in EAP45 (GLUE) protein. C-peptide helix-grafted GLUE selectively binds a mimic of the N-terminal helical region of gp41, a well-established HIV drug target, in a complex cellular environment. Additionally, the helix-grafted GLUE is folded in solution, stable in human serum, and soluble in aqueous solutions, and thus overcomes challenges faced by a multitude of peptide drugs, including those derived from HIV gp41 C-peptide.Entities:
Keywords: HIV/AIDS; gp41; helix grafting; protein engineering; protein-protein interactions
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Year: 2014 PMID: 25477243 PMCID: PMC4470567 DOI: 10.1002/cbic.201402531
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164