کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2510926 1117995 2010 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
A peptide derived from hepatitis C virus E2 envelope protein inhibits a post-binding step in HCV entry
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ویروس شناسی
پیش نمایش صفحه اول مقاله
A peptide derived from hepatitis C virus E2 envelope protein inhibits a post-binding step in HCV entry
چکیده انگلیسی

The HCV envelope proteins E1 and E2 are required for virus binding to cellular receptors and pH-dependent fusion with endosomal membranes. Envelope protein interactions within this multistep process may provide novel targets for development of antiviral agents. To identify E1 and E2 regions involved in critical steps of HCV entry, we screened an E1E2 overlapping peptide library for inhibition of infection using a lentiviral reporter vector pseudotyped with E1E2 envelope proteins. A 16-residue polypeptide containing a portion of the E2 transmembrane domain (Peptide 75) inhibited HCV pseudoparticle infection with an IC50 of approximately 0.3 μM and did not inhibit infection by VSV-g pseudoparticles at concentrations up to 50 μM. Structure–activity analysis of Peptide 75 showed that antiviral activity was dependent upon L-configuration and hydrophobic character, and that the native sequence was required for maximal activity. Peptide 75 did not show virocidal activity against HCV pseudoparticles or other viruses. Temperature-shift experiments showed that the peptide acted at a post-binding step and that inhibition was further increased when used in combination with an anti-CD81 antibody previously shown to inhibit pseudoparticle entry at a post-binding step. These data suggest that interactions involving the C terminal region of E2 may play an important role in the HCV entry process.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Antiviral Research - Volume 86, Issue 2, May 2010, Pages 172–179
نویسندگان
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