Department of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, NY, USA.
J Mol Biol. 2012 Jan 13;415(2):248-62. doi: 10.1016/j.jmb.2011.11.014. Epub 2011 Nov 12.
Prolonged highly active anti-retroviral therapy with multiple nucleoside reverse transcriptase inhibitors for the treatment of patients infected with human immunodeficiency virus type 1 (HIV-1) can induce the development of an HIV-1 reverse transcriptase (RT) harboring a dipeptide insertion at the RT fingers domain with a background thymidine analog mutation. This mutation renders viral resistance to multiple nucleoside reverse transcriptase inhibitors. We investigated the effect of the dipeptide fingers domain insertion mutation on strand transfer activity using two clinical RT variants isolated during the pre-treatment and post-treatment of an infected patient, termed pre-drug RT without dipeptide insertion and post-drug RT with Ser-Gly insertion, respectively. First, the post-drug RT displayed elevated strand transfer activity compared to the pre-drug RT, with two different RNA templates. Second, the post-drug RT exhibited less RNA template degradation than the pre-drug RT but higher polymerization-dependent RNase H activity. Third, the post-drug RT had a faster association rate (k(on)) for template binding and a lower equilibrium binding constant K(d) for the template, leading to a template binding affinity tighter than that of the pre-drug RT. The k(off) values for the pre-drug RT and the post-drug RT were similar. Finally, the removal of the dipeptide insertion from the post-drug RT abolished the elevated strand transfer activity and RNase H activity, in addition to the loss of azidothymidine resistance. These biochemical data suggest that the dipeptide insertion elevates strand transfer activity by increasing the interaction of the RT with the RNA donor template, promoting cleavage that generates more invasion sites for the acceptor template during DNA synthesis.
长期使用多种核苷逆转录酶抑制剂进行高效抗逆转录病毒治疗,可诱导人类免疫缺陷病毒 1 型(HIV-1)逆转录酶(RT)出现二肽插入突变,该突变使病毒对多种核苷逆转录酶抑制剂产生耐药性。我们使用在感染患者治疗前和治疗后分离得到的两种临床 RT 变异体(分别称为无插入二肽的治疗前 RT 和含有 Ser-Gly 插入的治疗后 RT),研究了二肽插入对链转移活性的影响。首先,与治疗前 RT 相比,治疗后 RT 与两种不同的 RNA 模板结合时显示出更高的链转移活性。其次,治疗后 RT 的 RNA 模板降解程度低于治疗前 RT,但聚合酶依赖性 RNase H 活性更高。第三,治疗后 RT 具有更快的模板结合速率(k(on))和更低的模板结合平衡常数 K(d),从而导致其与模板的结合亲和力强于治疗前 RT。治疗前 RT 和治疗后 RT 的 k(off)值相似。最后,从治疗后 RT 中去除二肽插入消除了其增强的链转移活性和 RNase H 活性,同时也失去了齐多夫定的耐药性。这些生化数据表明,二肽插入通过增加 RT 与 RNA 供体模板的相互作用,促进了在 DNA 合成过程中产生更多的入侵位点,从而提高了链转移活性。