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猴免疫缺陷病毒包膜恒定区3和4突变的影响。

Effects of mutations in constant regions 3 and 4 of envelope of simian immunodeficiency virus.

作者信息

Morrison H G, Kirchhoff F, Desrosiers R C

机构信息

New England Regional Primate Research Center, Harvard Medical School, Southborough, Massachusetts 01772-9102, USA.

出版信息

Virology. 1995 Jul 10;210(2):448-55. doi: 10.1006/viro.1995.1361.

Abstract

Twenty-six mutant forms of simian immunodeficiency virus strain mac239 were constructed with changes in constant region 4 (C4) of env. Twenty-four of these had a single amino acid change, one had changes in two amino acids, and one had a deletion of eight amino acids. The effects of these mutations on viral replication, gp160 processing, and binding of env protein to soluble CD4 receptor were analyzed. The C4 region was relatively sensitive to sequence changes since only 11 of the 26 mutants replicated appreciably. Eight of the 15 mutants that were replication incompetent exhibited grossly defective processing of the gp160 env precursor; these mutations likely resulted in global effects on gp160 structure. Six of the replication incompetent mutants exhibited normal or near normal gp160 processing and binding of env protein to sCD4 and thus were probably blocked at some step subsequent to binding of virus to its CD4 receptor. Only one of the C4 mutations, 441W-->R, resulted in greatly decreased binding to sCD4 while retaining normal processing of gp160. The equivalent residue in HIV-1 has similarly been shown previously to be important for binding of HIV-1 to the CD4 receptor. Since a W-->S mutation at position 441 in C4 of SIVmac239 affected both gp160 processing and sCD4 binding, it is not clear whether the 441 tryptophan is actually important for contacting CD4 or for maintaining an appropriate configuration. mutations within a highly conserved GGDPE sequence in C3 of SIVmac239 specifically affected CD4 binding, which is also similar to previous findings with HIV-1. These results demonstrate similar sequence requirements in SIVmac and HIV-1 env for binding C4, but they raise doubts as to whether C4 sequences are directly involved in the binding.

摘要

构建了26种猿猴免疫缺陷病毒株mac239的突变形式,其env基因的恒定区4(C4)发生了变化。其中24种有单个氨基酸变化,1种有两个氨基酸变化,1种有8个氨基酸缺失。分析了这些突变对病毒复制、gp160加工以及env蛋白与可溶性CD4受体结合的影响。C4区域对序列变化相对敏感,因为26个突变体中只有11个能显著复制。15个无复制能力的突变体中有8个对gp160 env前体的加工存在严重缺陷;这些突变可能对gp160结构产生全局性影响。6个无复制能力的突变体表现出正常或接近正常的gp160加工以及env蛋白与sCD4的结合,因此可能在病毒与CD4受体结合后的某个步骤受阻。只有C4突变体441W→R导致与sCD4的结合大幅减少,同时保持gp160的正常加工。此前已证明HIV-1中的等效残基对HIV-1与CD4受体的结合同样重要。由于SIVmac239的C4中441位的W→S突变影响了gp160加工和sCD4结合,目前尚不清楚441位色氨酸对于接触CD4或维持适当构象是否真的重要。SIVmac239的C3中高度保守的GGDPE序列内的突变特异性地影响了CD4结合,这也与之前对HIV-1的研究结果相似。这些结果表明,SIVmac和HIV-1 env在结合C4方面有相似的序列要求,但它们对C4序列是否直接参与结合提出了疑问。

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