Herschlag D, Cech T R
Department of Chemistry and Biochemistry, Howard Hughes Medical Institute, University of Colorado, Boulder 80309-0215.
Biochemistry. 1990 Nov 6;29(44):10172-80. doi: 10.1021/bi00496a004.
The site-specific endonuclease reaction catalyzed by the ribozyme from the Tetrahymena pre-rRNA intervening sequence has been characterized with a substrate that forms a "matched" duplex with the 5' exon binding site of the ribozyme [G2CCCUCUA5 + G in equilibrium with G2CCCUCU + GA5 (G = guanosine); Herschlag, D., & Cech, T.R. (1990) Biochemistry (preceding paper in this issue)]. The rate-limiting step with saturating substrate is dissociation of the product G2CCCUCU. Here we show that the reaction of the substrate G2CCCGCUA5, which forms a "mismatched" duplex with the 5' exon binding site at position -3 from the cleavage site, has a value of kcat that is approximately 10(2)-fold greater than kcat for the matched substrate (50 degrees C, 10 mM MgCl2, pH 7). This is explained by the faster dissociation of the mismatched product, G2CCCGCU, than the matched product. With subsaturating oligonucleotide substrate and saturating G, the binding of the oligonucleotide substrate and the chemical step are each partially rate-limiting. The rate constant for the chemical step of the endonuclease reaction and the rate constant for the site-specific hydrolysis reaction, in which solvent replaces G, are each within approximately 2-fold with the matched and mismatched substrates, despite the approximately 10(3)-fold weaker binding of the mismatched substrate. This can be described as "uniform binding" of the base at position -3 in the ground state and transition state [Albery, W.J., & Knowles, J. R. (1976) Biochemistry 15, 5631-5640]. Thus, the matched substrate does not use its extra binding energy to preferentially stabilize the transition state.(ABSTRACT TRUNCATED AT 250 WORDS)
由四膜虫前体rRNA间隔序列的核酶催化的位点特异性内切核酸酶反应,已通过一种与核酶5'外显子结合位点形成“匹配”双链体的底物进行了表征[G2CCCUCUA5 + G与G2CCCUCU + GA5处于平衡状态(G = 鸟苷);赫施拉格,D.,& 切赫,T.R.(1990年)《生物化学》(本期之前的论文)]。底物饱和时的限速步骤是产物G2CCCUCU的解离。在此我们表明,底物G2CCCGCUA5与切割位点上游-3位的5'外显子结合位点形成“错配”双链体,其催化常数kcat的值比匹配底物的kcat大约大100倍(50℃,10 mM MgCl2,pH 7)。这是由于错配产物G2CCCGCU的解离比匹配产物更快。对于亚饱和的寡核苷酸底物和饱和的G,寡核苷酸底物的结合和化学步骤各自部分限速。内切核酸酶反应化学步骤的速率常数以及溶剂取代G的位点特异性水解反应的速率常数,在匹配和错配底物的情况下,各自都在大约2倍的范围内,尽管错配底物的结合弱大约1000倍。这可以描述为基态和过渡态中-3位碱基的“均匀结合”[阿尔贝里,W.J.,& 诺尔斯,J.R.(1976年)《生物化学》15,5631 - 5640]。因此,匹配底物不会利用其额外的结合能来优先稳定过渡态。(摘要截断于250字)