Donnelly M Lauren, Forster Emily R, Rohlfing Amy E, Shen Aimee
Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts, U.S.A.
Graduate School of Biomedical Sciences, Tufts University School of Medicine, Boston, Massachusetts, U.S.A.
Biochem J. 2020 Apr 30;477(8):1459-1478. doi: 10.1042/BCJ20190875.
Clostridioides difficile is a spore-forming bacterial pathogen that is the leading cause of hospital-acquired gastroenteritis. C. difficile infections begin when its spore form germinates in the gut upon sensing bile acids. These germinants induce a proteolytic signaling cascade controlled by three members of the subtilisin-like serine protease family, CspA, CspB, and CspC. Notably, even though CspC and CspA are both pseudoproteases, they are nevertheless required to sense germinants and activate the protease, CspB. Thus, CspC and CspA are part of a growing list of pseudoenzymes that play important roles in regulating cellular processes. However, despite their importance, the structural properties of pseudoenzymes that allow them to function as regulators remain poorly understood. Our recently solved crystal structure of CspC revealed that its pseudoactive site residues align closely with the catalytic triad of CspB, suggesting that it might be possible to 'resurrect' the ancestral protease activity of the CspC and CspA pseudoproteases. Here, we demonstrate that restoring the catalytic triad to these pseudoproteases fails to resurrect their protease activity. We further show that the pseudoactive site substitutions differentially affect the stability and function of the CspC and CspA pseudoproteases: the substitutions destabilized CspC and impaired spore germination without affecting CspA stability or function. Thus, our results surprisingly reveal that the presence of a catalytic triad does not necessarily predict protease activity. Since homologs of C. difficile CspA occasionally carry an intact catalytic triad, our results indicate that bioinformatic predictions of enzyme activity may underestimate pseudoenzymes in rare cases.
艰难梭菌是一种形成孢子的细菌病原体,是医院获得性肠胃炎的主要病因。当艰难梭菌的孢子形式在肠道中感知到胆汁酸时就会萌发,从而引发感染。这些萌发剂会诱导一个由枯草杆菌蛋白酶样丝氨酸蛋白酶家族的三个成员CspA、CspB和CspC控制的蛋白水解信号级联反应。值得注意的是,尽管CspC和CspA都是假蛋白酶,但它们仍然需要感知萌发剂并激活蛋白酶CspB。因此,CspC和CspA是越来越多在调节细胞过程中发挥重要作用的假酶中的一部分。然而,尽管它们很重要,但假酶能够作为调节因子发挥作用的结构特性仍然知之甚少。我们最近解析的CspC晶体结构表明,其假活性位点残基与CspB的催化三联体紧密对齐,这表明有可能“复活”CspC和CspA假蛋白酶的祖先蛋白酶活性。在这里,我们证明将催化三联体恢复到这些假蛋白酶中并不能恢复它们的蛋白酶活性。我们进一步表明,假活性位点的替换对CspC和CspA假蛋白酶的稳定性和功能有不同的影响:这些替换使CspC不稳定并损害孢子萌发,而不影响CspA的稳定性或功能。因此,我们的结果令人惊讶地表明,催化三联体的存在并不一定预示着蛋白酶活性。由于艰难梭菌CspA的同源物偶尔会携带完整的催化三联体,我们的结果表明,在罕见情况下,酶活性的生物信息学预测可能会低估假酶。