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靶向HIV-1 gp41 N端和C端螺旋区域的抑制剂揭示了HIV-1包膜糖蛋白介导融合过程中与温度相关的中间体。

Temperature-dependent intermediates in HIV-1 envelope glycoprotein-mediated fusion revealed by inhibitors that target N- and C-terminal helical regions of HIV-1 gp41.

作者信息

Gallo Stephen A, Clore G Marius, Louis John M, Bewley Carole A, Blumenthal Robert

机构信息

Laboratory of Experimental and Computational Biology, National Cancer Institute, National Institutes of Health, Frederick, Maryland 21702, USA.

出版信息

Biochemistry. 2004 Jun 29;43(25):8230-3. doi: 10.1021/bi049957v.

Abstract

Peptides derived from the N- (N-HR) and C- (C-HR) terminal heptad repeat regions adjacent to the fusion peptide and transmembrane domains, respectively, of human immunodeficiency virus (HIV)-1 gp41 inhibit HIV-1 viral envelope glycoproteins (Env)-mediated cell fusion specifically. The mechanism of HIV-1 Env-mediated cell fusion and its inhibition by agents that target the N- and C-HR regions was investigated. Priming experiments with Env-expressing cells indicate that the N-HR region but not the C-HR region is exposed by treatment with sCD4 at 31 degrees C, whereas both the N- and C-HR regions are exposed at 37 degrees C.

摘要

分别源自人免疫缺陷病毒(HIV)-1 gp41融合肽和跨膜结构域附近的N-(N-HR)和C-(C-HR)末端七肽重复区域的肽,可特异性抑制HIV-1病毒包膜糖蛋白(Env)介导的细胞融合。研究了HIV-1 Env介导的细胞融合机制及其被靶向N-和C-HR区域的试剂抑制的情况。用表达Env的细胞进行的引发实验表明,在31℃用可溶性CD4(sCD4)处理可使N-HR区域暴露,而C-HR区域不暴露,而在37℃时N-和C-HR区域均暴露。

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