Gopalakrishnan V, Peliska J A, Benkovic S J
Department of Chemistry, Pennsylvania State University, University Park 16802.
Proc Natl Acad Sci U S A. 1992 Nov 15;89(22):10763-7. doi: 10.1073/pnas.89.22.10763.
The spatial and temporal relationship between the polymerase and RNase H activities of human immunodeficiency virus type 1 reverse transcriptase has been examined by using a 40-mer RNA template and a series of DNA primers of lengths ranging from 15 to 40 nucleotides, hybridized to the RNA, as substrates. The experiments were executed in the absence and presence of heparin, an efficient trap to sequester any free or dissociated reverse transcriptase, thus facilitating the study of events associated with a single turnover of the enzyme. The results indicate a spatial separation of 18 or 19 nucleotides between the two sites. To examine the effect of concomitant polymerization on the RNase H activity, the substrate was doubly 5' end labeled on the RNA and DNA. This enabled the study of RNase H activity as a function of polymerization in a single experiment, and the results in the absence and presence of heparin indicate a tight temporal coupling between the two activities.
通过使用一个40聚体RNA模板和一系列长度从15到40个核苷酸不等、与该RNA杂交的DNA引物作为底物,对1型人类免疫缺陷病毒逆转录酶的聚合酶活性和核糖核酸酶H活性之间的时空关系进行了研究。实验在不存在和存在肝素的情况下进行,肝素是一种有效的捕获剂,可隔离任何游离或解离的逆转录酶,从而便于研究与该酶单次周转相关的事件。结果表明两个位点之间在空间上相隔18或19个核苷酸。为了研究伴随聚合对核糖核酸酶H活性的影响,底物在RNA和DNA的5'端进行了双重标记。这使得能够在单个实验中研究核糖核酸酶H活性作为聚合作用的函数,并且在不存在和存在肝素的情况下的结果表明这两种活性之间存在紧密的时间耦合。