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2L6S

Efficacy of an HIV-1 entry inhibitor targeting the GP41 fusion peptide

2L6S の概要
エントリーDOI10.2210/pdb2l6s/pdb
関連するPDBエントリー2JNR 2L6T
分子名称VIR-576 (1 entity in total)
機能のキーワードanti-viral polypeptide, antiviral protein
タンパク質・核酸の鎖数1
化学式量合計2252.69
構造登録者
主引用文献Forssmann, W.G.,The, Y.H.,Stoll, M.,Adermann, K.,Albrecht, U.,Barlos, K.,Busmann, A.,Canales-Mayordomo, A.,Gimenez-Gallego, G.,Hirsch, J.,Jimenez-Barbero, J.,Meyer-Olson, D.,Munch, J.,Perez-Castells, J.,Standker, L.,Kirchhoff, F.,Schmidt, R.E.
Short-term monotherapy in HIV-infected patients with a virus entry inhibitor against the gp41 fusion peptide.
Sci Transl Med, 2:63re3-63re3, 2010
Cited by
PubMed Abstract: To infect host cells, most enveloped viruses must insert a hydrophobic fusion peptide into the host cell membrane. Thus, fusion peptides may be valuable targets for developing drugs that block virus entry. We have shown previously that a natural 20-residue fragment of α(1)-antitrypsin, designated VIRus-Inhibitory Peptide (VIRIP), that binds to the gp41 fusion peptide of HIV-1 prevents the virus from entering target cells in vitro. Here, we examine the efficacy of 10-day monotherapy with the optimized VIR-576 derivative of VIRIP in treatment-naïve, HIV-1-infected individuals with viral RNA loads of ≥10,000 copies per ml. We report that at the highest dose (5.0 grams per day), intravenous infusion of VIR-576 reduced the mean plasma viral load by 1.23 log(10) copies per ml without causing severe adverse effects. Our results are proof of concept that fusion peptide inhibitors suppress viral replication in human patients, and offer prospects for the development of a new class of drugs that prevent virus particles from anchoring to and infecting host cells.
PubMed: 21178138
DOI: 10.1126/scitranslmed.3001697
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 2l6s
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件を2025-12-31に公開中

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