Rosen Osnat, Samson Avraham O, Anglister Jacob
Department of Structural Biology, Weizmann Institute of Science, Rehovot 76100, Israel.
Proteins. 2008 May 15;71(3):1066-70. doi: 10.1002/prot.21982.
Analysis of V3 and C4 sequences of HIV-1 reveals correlated mutations at gp120 positions 322 and 440, and a very strong preference for a positively charged residue at position 440 when position 322 is negatively charged. This observation suggests that these two residues are close to each other and interact electrostatically in R5 viruses. This interaction was used to model V3 in the context of gp120 using NMR data for the V3 loop and the crystal structure of the gp120-core. The interaction between residues 322 and 440 may serve as part of the molecular switch for HIV-1 phenotype conversion.
对HIV-1的V3和C4序列分析显示,在gp120的322位和440位存在相关突变,并且当322位带负电荷时,440位强烈倾向于带正电荷的残基。这一观察结果表明,在R5病毒中这两个残基彼此靠近并通过静电相互作用。利用V3环的核磁共振数据和gp120核心的晶体结构,这种相互作用被用于在gp120背景下对V3进行建模。322位和440位残基之间的相互作用可能作为HIV-1表型转换分子开关的一部分。