2L6S
Efficacy of an HIV-1 entry inhibitor targeting the GP41 fusion peptide
2L6S の概要
| エントリーDOI | 10.2210/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 | Forssmann, W.,The, Y.,Stoll, M.,Adermann, K.,Albrecht, U.,Barlos, K.,Busmann, A.,Canales-Mayordomo, A.,Gimenez-Gallego, G.,Hirsch, J.,Jimenez-Barbero, J.,Meyer-Olson, D.,Muench, J.,Perez-Castells, J.,Standker, L.,Kirchhoff, F.,Schmidt, R.E. (登録日: 2010-11-24, 公開日: 2011-01-19, 最終更新日: 2024-05-01) |
| 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: 21178138DOI: 10.1126/scitranslmed.3001697 主引用文献が同じPDBエントリー |
| 実験手法 | SOLUTION NMR |
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