Garforth Scott J, Domaoal Robert A, Lwatula Chisanga, Landau Mark J, Meyer Amanda J, Anderson Karen S, Prasad Vinayaka R
Department of Microbiology and Immunology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
J Mol Biol. 2010 Aug 6;401(1):33-44. doi: 10.1016/j.jmb.2010.06.001. Epub 2010 Jun 9.
Lys65 residue, in the fingers domain of human immunodeficiency virus reverse transcriptase (RT), interacts with incoming dNTP in a sequence-independent fashion. We showed previously that a 5-amino-acid deletion spanning Lys65 and a K65A substitution both enhanced the fidelity of dNTP insertion. We hypothesized that the Lys65 residue enhances dNTP misinsertion via interactions with the gamma-phosphate of the incoming dNTP. We now examine this hypothesis in pre-steady-state kinetic studies using wild-type human immunodeficiency virus-1 RT and two substitution mutants, K65A and K65R. K65R mutation did not greatly increase misinsertion fidelity, but K65A mutation led to higher incorporation fidelity. For a misinsertion to become a permanent error, it needs to be accompanied by the extension of the mispaired terminus thus formed. Both mutants and the wild-type enzyme discriminated against the mismatched primer at the catalytic step (k(pol)). Additionally, K65A and K65R mutants displayed a further decrease in mismatch extension efficiency, primarily at the level of dNTP binding. We employed hydroxyl radical footprinting to determine the position of the RT on the primer/template. The wild-type and Lys65-substituted enzymes occupied the same position at the primer terminus; the presence of a mismatched primer terminus caused all three enzymes to be displaced to a -2 position relative to the primer 3' end. In the context of an efficiently extended mismatched terminus, the presence of the next complementary nucleotide overcame the displacement, resulting in a complex resembling the matched terminus. The results are consistent with the observed reduction in k(pol) in mispaired primer extension being due to the position of the enzyme at a mismatched terminus. Our work shows the influence of the stabilizing interactions of Lys65 with the incoming dNTP on two different aspects of polymerase fidelity.
人类免疫缺陷病毒逆转录酶(RT)指状结构域中的赖氨酸65(Lys65)残基以序列非依赖的方式与进入的脱氧核苷三磷酸(dNTP)相互作用。我们之前表明,跨越Lys65的5个氨基酸缺失以及K65A取代均增强了dNTP插入的保真度。我们推测Lys65残基通过与进入的dNTP的γ-磷酸基团相互作用增强了dNTP的错配插入。我们现在使用野生型人类免疫缺陷病毒1型RT以及两个取代突变体K65A和K65R,在预稳态动力学研究中检验这一推测。K65R突变并未大幅提高错配插入保真度,但K65A突变导致更高的掺入保真度。要使错配插入成为永久性错误,它需要伴随着由此形成的错配末端的延伸。突变体和野生型酶在催化步骤(k(pol))均区分错配引物。此外,K65A和K65R突变体显示错配延伸效率进一步降低,主要在dNTP结合水平。我们采用羟基自由基足迹法来确定RT在引物/模板上的位置。野生型和Lys65取代的酶在引物末端占据相同位置;错配引物末端的存在导致所有三种酶相对于引物3'端移位至 -2位置。在有效延伸的错配末端的情况下,下一个互补核苷酸的存在克服了移位,产生了类似于匹配末端的复合物。结果与观察到的错配引物延伸中k(pol)的降低是由于酶在错配末端的位置一致。我们的工作表明Lys65与进入的dNTP的稳定相互作用对聚合酶保真度的两个不同方面的影响。