Defining the DNA Substrate Binding Sites on HIV-1 Integrase

被引:23
作者
Dolan, James [1 ]
Chen, Aiping [1 ]
Weber, Irene T. [2 ]
Harrison, Robert W. [3 ]
Leis, Jonathan [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Microbiol & Immunol, Chicago, IL 60611 USA
[2] Georgia State Univ, Dept Biol, Atlanta, GA 30303 USA
[3] Georgia State Univ, Dept Comp Sci, Atlanta, GA 30303 USA
关键词
HIV-1; integrase; model structure; DNA; IMMUNODEFICIENCY-VIRUS TYPE-1; MOLECULAR-MECHANICS CALCULATIONS; STRUCTURE-BASED MUTAGENESIS; IN-VITRO; VIRAL-DNA; TERMINAL SEQUENCES; STRAND TRANSFER; ACTIVE-SITE; DIKETO ACID; LEDGF/P75;
D O I
10.1016/j.jmb.2008.10.083
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A tetramer model for human immunodeficiency virus type 1. (HIV-1) integrase (IN) with DNA representing long terminal repeat (LTR) termini was previously assembled to predict the IN residues that interact with the LTR termini; these predictions were experimentally verified for nine amino acid residues [Chen, A., Weber, 1. T., Harrison, R. W. & Leis, J. (2006). Identification of amino acids in HIV-1 and avian sarcoma virus integrase subsites required for specific recognition of the long terminal repeat ends. J. Biol. Chem., 281, 4173-4182]. In a similar strategy, the unique amino acids found in avian sarcoma virus IN, rather than HWA or Mason-Pfizer monkey virus IN, were substituted into the structurally related positions of HIV-1 IN. Substitutions of six additional residues (Q44, L68, E69, D229, S230, and D253) showed changes in the 3' processing specificity of the enzyme, verifying their predicted interaction with the LTR DNA. The newly identified residues extend interactions along a 16-bp length of the LTR termini and are consistent with known LTR DNA/HIV-1 IN cross-links. The tetramer model for HIV-1 IN with LTR termini was modified to include two IN binding domains for lens-epithelium-derived growth factor/p75. The target DNA was predicted to bind in a surface trench perpendicular to the plane of the LTR DNA binding sites of HIV-1 IN and extending alongside lens-epithelium-derived growth factor. This hypothesis is supported by the in vitro activity phenotype of HIV-1 IN mutant, with a K219S substitution showing loss in strand transfer activity while maintaining 3' processing on an HIV-1 substrate. Mutations at seven other residues reported in the literature have the same phenotype, and all eight residues align along the length of the putative target DNA binding trench. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:568 / 579
页数:12
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