Semler B L, Johnson V H, Dewalt P G, Ypma-Wong M F
J Cell Biochem. 1987 Jan;33(1):39-51. doi: 10.1002/jcb.240330105.
The cleavage of poliovirus precursor polypeptides occurs at specific amino acid pairs that are recognized by viral proteinases. Most of the polio-specific cleavages occur at glutamine-glycine (Q-G) pairs that are recognized by the viral-encoded proteinase 3C (formerly called P3-7c). In order to carry out a defined molecular genetic study of the enzymatic activity of protein 3C, we have made cDNA clones of the poliovirus genome. The cDNA region corresponding to protein 3C was inserted into an inducible bacterial expression vector. This recombinant plasmid (called pIN-III-C3-7c) utilizes the bacterial lipoprotein promoter to direct the synthesis of a precursor polypeptide that contains the amino acid sequence of protein 3C as well as the amino- and carboxy-terminal Q-G cleavage signals. These signals have been previously shown to allow autocatalytic production of protein 3C in bacteria transformed with plasmid pIN-III-C3-7c. We have taken advantage of the autocatalytic cleavage of 3C in a bacterial expression system to study the effects of site-specific mutagenesis on its proteolytic activity. One mutation that we have introduced into the cDNA region encoding 3C is a single amino acid insertion near the carboxy-terminal Q-G cleavage site. The mutant recombinant plasmid (designated pIN-III-C3-mu 10) directs the synthesis of a bacterial-polio precursor polypeptide that is like the wild-type construct (pIN-III-C3-7c). However, unlike the wild-type precursor, the mutant precursor cannot undergo autocatalytic cleavage to generate the mature proteinase 3C. Rather, the precursor is able to carry out cleavage at the amino-terminal Q-G site but not at the carboxy-terminal site. Thus, we have generated an altered poliovirus proteinase that is still able to carry out at least part of its cleavage activities but is unable to be a suitable substrate for self-cleavage at its carboxy-terminal Q-G pair.
脊髓灰质炎病毒前体多肽的切割发生在病毒蛋白酶识别的特定氨基酸对处。大多数脊髓灰质炎特异性切割发生在谷氨酰胺 - 甘氨酸(Q - G)对处,这些位点由病毒编码的蛋白酶3C(以前称为P3 - 7c)识别。为了对蛋白3C的酶活性进行明确的分子遗传学研究,我们构建了脊髓灰质炎病毒基因组的cDNA克隆。将与蛋白3C对应的cDNA区域插入到一个可诱导的细菌表达载体中。这个重组质粒(称为pIN - III - C3 - 7c)利用细菌脂蛋白启动子来指导一种前体多肽的合成,该前体多肽包含蛋白3C的氨基酸序列以及氨基和羧基末端的Q - G切割信号。这些信号先前已被证明能使在质粒pIN - III - C3 - 7c转化的细菌中自动催化产生蛋白3C。我们利用细菌表达系统中3C的自动催化切割来研究位点特异性诱变对其蛋白水解活性的影响。我们在编码3C的cDNA区域引入的一个突变是在羧基末端Q - G切割位点附近插入一个单一氨基酸。突变重组质粒(命名为pIN - III - C3 - mu 10)指导合成一种细菌 - 脊髓灰质炎前体多肽,它类似于野生型构建体(pIN - III - C3 - 7c)。然而,与野生型前体不同,突变前体不能进行自动催化切割以产生成熟的蛋白酶3C。相反,该前体能够在氨基末端的Q - G位点进行切割,但不能在羧基末端位点切割。因此,我们产生了一种改变的脊髓灰质炎病毒蛋白酶,它仍然能够进行至少部分切割活性,但不能成为其羧基末端Q - G对自我切割的合适底物。