5HFM
Gp41-targeting HIV-1 fusion inhibitors with hook-like Ile-Asp-Leu tail
5HFM の概要
| エントリーDOI | 10.2210/pdb5hfm/pdb |
| 関連するPDBエントリー | 5HFL |
| 分子名称 | Envelope glycoprotein gp160,gp41 CHR region, TRIS(HYDROXYETHYL)AMINOMETHANE (3 entities in total) |
| 機能のキーワード | hiv-1 fusion inhibitor, ile-asp-leu tail, hook-like tail, viral protein |
| 由来する生物種 | Human immunodeficiency virus 1 (HIV-1) 詳細 |
| タンパク質・核酸の鎖数 | 6 |
| 化学式量合計 | 57007.50 |
| 構造登録者 | |
| 主引用文献 | Zhu, Y.,Su, S.,Qin, L.,Wang, Q.,Shi, L.,Ma, Z.,Tang, J.,Jiang, S.,Lu, L.,Ye, S.,Zhang, R. Rational improvement of gp41-targeting HIV-1 fusion inhibitors: an innovatively designed Ile-Asp-Leu tail with alternative conformations Sci Rep, 6:31983-31983, 2016 Cited by PubMed Abstract: Peptides derived from the C-terminal heptad repeat (CHR) of HIV gp41 have been developed as effective fusion inhibitors against HIV-1, but facing the challenges of enhancing potency and stability. Here, we report a rationally designed novel HIV-1 fusion inhibitor derived from CHR-derived peptide (Trp628~Gln653, named CP), but with an innovative Ile-Asp-Leu tail (IDL) that dramatically increased the inhibitory activity by up to 100 folds. We also determined the crystal structures of artificial fusion peptides N36- and N43-L6-CP-IDL. Although the overall structures of both fusion peptides share the canonical six-helix bundle (6-HB) configuration, their IDL tails adopt two different conformations: a one-turn helix with the N36, and a hook-like structure with the longer N43. Structural comparison showed that the hook-like IDL tail possesses a larger interaction interface with NHR than the helical one. Further molecular dynamics simulations of the two 6-HBs and isolated CP-IDL peptides suggested that hook-like form of IDL tail can be stabilized by its binding to NHR trimer. Therefore, CP-IDL has potential for further development as a new HIV fusion inhibitor, and this strategy could be widely used in developing artificial fusion inhibitors against HIV and other enveloped viruses. PubMed: 27666394DOI: 10.1038/srep31983 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.298 Å) |
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