Krug M S, Berger S L
Section on Genes and Gene Products, National Cancer Institute, NIH, Bethesda, MD 20892.
Biochemistry. 1991 Nov 5;30(44):10614-23. doi: 10.1021/bi00108a003.
The binding of substrates to recombinant reverse transcriptase from human immunodeficiency virus (HIV) and the natural enzyme from avian myeloblastosis virus (AMV) has been examined by analyzing both the ribonuclease H and the RNA-dependent DNA polymerase activities. With 3'-end-labeled globin mRNA hybridized to (dT)15 as the substrate in the ribonuclease H reaction, the enzymes partially deadenylated the mRNA in a distributive manner. Under these conditions, there was a rapid initial burst followed by a prolonged, but much slower, steady-state rate. The biphasic reaction made possible determinations of kinetic constants as follows: values for Km, KD, and kcat were, respectively, 27 nM, 11 nM, and 5 x 10(-3) s-1 for the HIV enzyme and 30 nM, 9 nM, and 5 x 10(-3) s-1, respectively, for the avian enzyme. These constants were used to derive other parameters: The rate of association of the template-primer with reverse transcriptase was approximately 2 x 10(5) M-1 s-1, and the rate of dissociation was approximately 2 x 10(-3) s-1, regardless of the source of the enzyme. The rate of release of the product was essentially equivalent to the value of kcat indicated above for each of the enzymes. The polymerase reaction was evaluated under processive conditions of synthesis; values of Km and kcat of approximately 6 nM and approximately 2.5 s-1, respectively, for the human enzyme, and approximately 10 nM and approximately 2 s-1, respectively, for the avian enzyme were observed. The interaction of substrates with HIV reverse transcriptase was characterized further with the aid of ribonucleoside-vanadyl complexes. These complexes inhibited the polymerase and ribonuclease H activities of the enzyme competitively with respect to globin mRNA.(dT)15. Values of Ki ranging from 1 to 3 mM were obtained. With respect to deoxyribonucleoside triphosphate substrates in the polymerase reaction, mixed inhibition was observed. Deoxyribonucleoside triphosphates had no effect on kinetic parameters governing the ribonuclease H activity of the HIV enzyme but apparently facilitated the formation of active enzyme. These data fit a model in which one template-primer binding site serves both the polymerase and the ribonuclease H catalytic sites.
通过分析核糖核酸酶H和依赖RNA的DNA聚合酶活性,研究了底物与人免疫缺陷病毒(HIV)重组逆转录酶以及禽成髓细胞瘤病毒(AMV)天然酶的结合情况。在核糖核酸酶H反应中,以与(dT)15杂交的3'末端标记的珠蛋白mRNA作为底物,这些酶以分布的方式使mRNA部分去腺苷酸化。在这些条件下,反应呈现出快速的初始爆发,随后是延长但缓慢得多的稳态速率。这种双相反应使得动力学常数的测定成为可能,结果如下:HIV酶的Km、KD和kcat值分别为27 nM、11 nM和5×10⁻³ s⁻¹,禽酶的相应值分别为30 nM、9 nM和5×10⁻³ s⁻¹。这些常数被用于推导其他参数:模板引物与逆转录酶的结合速率约为2×10⁵ M⁻¹ s⁻¹,解离速率约为2×10⁻³ s⁻¹,与酶的来源无关。产物的释放速率基本上等同于上述每种酶的kcat值。在合成的持续条件下评估了聚合酶反应;观察到人类酶的Km和kcat值分别约为6 nM和约2.5 s⁻¹,禽酶的分别约为10 nM和约2 s⁻¹。借助核糖核苷 - 钒配合物进一步表征了底物与HIV逆转录酶的相互作用。这些配合物相对于珠蛋白mRNA·(dT)15竞争性地抑制了该酶的聚合酶和核糖核酸酶H活性。获得的Ki值范围为1至3 mM。对于聚合酶反应中的脱氧核苷三磷酸底物,观察到混合抑制作用。脱氧核苷三磷酸对控制HIV酶核糖核酸酶H活性的动力学参数没有影响,但显然促进了活性酶的形成。这些数据符合一个模型,其中一个模板引物结合位点同时服务于聚合酶和核糖核酸酶H催化位点。