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HIV进入宿主细胞的抑制剂。

Inhibitors of the entry of HIV into host cells.

作者信息

Meanwell Nicholas A, Kadow John F

机构信息

Bristol-Myers Squibb Pharmaceutical Research Institute, Department of Chemistry, 5 Research Parkway, Wallingford, CT 06492, USA.

出版信息

Curr Opin Drug Discov Devel. 2003 Jul;6(4):451-61.

Abstract

The development of mechanistic insight into the process by which HIV enters host cells has revealed a panoply of targets that offer considerable potential as sites for pharmacological intervention. The gp120/gp41 protein complex, expressed on the virion surface, mediates HIV entry by a process initiated by the engagement of the host cell receptor CD4. Subtle conformational changes triggered by this interaction expose elements of gp120 to the seven-transmembrane, G protein-coupled chemokine receptors CCR5 or CXCR4 expressed on host cells, a contact that relieves constraints imposed on gp41 by gp120. This leads to a major conformational rearrangement of gp41, which results in the insertion of the fusion peptide into the host cell membrane and the assembly of the amino terminus heptad repeat into a trimeric form that is subsequently recognized by the carboxy terminal heptad repeat. The latter process leads to juxtaposition of the viral and host cell membranes, a prelude to fusion. The most prominent strategies and targets that are actively being exploited as drug discovery opportunities are inhibition of the attachment of HIV to host cells, blockade of chemokine receptors and interference with the function of gp41. Inhibitors of each of these steps in the HIV entry process with potential clinical relevance are reviewed in the context of their status in the drug development process. The most significant entity to emerge from this area of research to date is enfuvirtide, a 36-amino acid derivative that interferes with the function of gp41. Enfuvirtide is the first HIV entry inhibitor to be granted a license for marketing (it was approved in the US and Europe in March 2003), and its introduction portends the beginning of what promises to be an exciting new era of HIV therapy.

摘要

对人类免疫缺陷病毒(HIV)进入宿主细胞过程的机制性深入了解,揭示了一系列极具潜力的靶点,有望成为药物干预的作用位点。病毒体表面表达的gp120/gp41蛋白复合物,通过与宿主细胞受体CD4结合启动的过程介导HIV进入。这种相互作用引发的细微构象变化,使gp120的某些元件暴露于宿主细胞表面表达的七跨膜G蛋白偶联趋化因子受体CCR5或CXCR4,这种接触解除了gp120对gp41施加的限制。这导致gp41发生重大构象重排,进而使融合肽插入宿主细胞膜,并使氨基末端七肽重复序列组装成三聚体形式,随后被羧基末端七肽重复序列识别。后一过程导致病毒膜与宿主细胞膜并列排列——这是融合之前的前奏(序幕)。目前作为药物研发机会而被积极开发利用的最突出策略和靶点包括抑制HIV与宿主细胞附着、阻断趋化因子受体以及干扰gp41的功能。本文将在HIV进入过程中这些步骤各自的抑制剂在药物研发进程中的现状背景下,对具有潜在临床意义的抑制剂进行综述。迄今为止,该研究领域出现的最重要药物是恩夫韦肽,一种干扰gp41功能的36个氨基酸的衍生物。恩夫韦肽是首个获得上市许可的HIV进入抑制剂(2003年3月在美国和欧洲获批)——它的问世预示着有望开启激动人心的HIV治疗新时代。

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