Department of Biochemistry, Case Western Reserve University, Cleveland, Ohio, United States of America.
Department of Molecular Biology and Microbiology, Case Western Reserve University, Cleveland, Ohio, United States of America ; Research Division, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, Ohio, United States of America.
PLoS One. 2014 Jan 16;9(1):e85892. doi: 10.1371/journal.pone.0085892. eCollection 2014.
β-Lactamases are the major reason β-lactam resistance is seen in Gram-negative bacteria. To combat this resistance mechanism, β-lactamase inhibitors are currently being developed. Presently, there are only three that are in clinical use (clavulanate, sulbactam and tazobactam). In order to address this important medical need, we explored a new inhibition strategy that takes advantage of a long-lived inhibitory trans-enamine intermediate. SA2-13 was previously synthesized and shown to have a lower k(react) than tazobactam. We investigated here the importance of the carboxyl linker length and composition by synthesizing three analogs of SA2-13 (PSR-4-157, PSR-4-155, and PSR-3-226). All SA2-13 analogs yielded higher turnover numbers and k(react) compared to SA2-13. We next demonstrated using protein crystallography that increasing the linker length by one carbon allowed for better capture of a trans-enamine intermediate; in contrast, this trans-enamine intermediate did not occur when the C2 linker length was decreased by one carbon. If the linker was altered by both shortening it and changing the carboxyl moiety into a neutral amide moiety, the stable trans-enamine intermediate in wt SHV-1 did not form; this intermediate could only be observed when a deacylation deficient E166A variant was studied. We subsequently studied SA2-13 against a relatively recently discovered inhibitor-resistant (IR) variant of SHV-1, SHV K234R. Despite the alteration in the mechanism of resistance due to the K→R change in this variant, SA2-13 was effective at inhibiting this IR enzyme and formed a trans-enamine inhibitory intermediate similar to the intermediate seen in the wt SHV-1 structure. Taken together, our data reveals that the C2 side chain linker length and composition profoundly affect the formation of the trans-enamine intermediate of penam sulfones. We also show that the design of SA2-13 derivatives offers promise against IR SHV β-lactamases that possess the K234R substitution.
β-内酰胺酶是革兰氏阴性菌产生β-内酰胺耐药性的主要原因。为了对抗这种耐药机制,目前正在开发β-内酰胺酶抑制剂。目前,只有三种β-内酰胺酶抑制剂在临床上使用(克拉维酸、舒巴坦和他唑巴坦)。为了满足这一重要的医疗需求,我们探索了一种新的抑制策略,利用了一种寿命长的抑制反式烯胺中间物。SA2-13 以前被合成并显示出比他唑巴坦更低的 k(react)。在这里,我们通过合成 SA2-13 的三个类似物(PSR-4-157、PSR-4-155 和 PSR-3-226)来研究羧基连接体长度和组成的重要性。所有 SA2-13 的类似物的周转率和 k(react)都比 SA2-13 高。接下来,我们通过蛋白质晶体学证明,增加连接体长度一个碳原子可以更好地捕获反式烯胺中间物;相反,当 C2 连接体长度缩短一个碳原子时,就不会发生这种反式烯胺中间物。如果连接体的长度缩短并且羧基部分变成中性酰胺部分,那么 wt SHV-1 中的稳定反式烯胺中间物就不会形成;只有当研究缺乏去酰化的 E166A 变体时,才能观察到这种中间物。随后,我们研究了 SA2-13 对最近发现的抑制剂耐药(IR)SHV-1 变体 SHV K234R 的抑制作用。尽管由于该变体中 K→R 的改变导致了耐药机制的改变,但 SA2-13 仍能有效抑制这种 IR 酶,并形成类似于 wt SHV-1 结构中观察到的反式烯胺抑制中间物。总之,我们的数据表明,C2 侧链连接体的长度和组成对 penam 磺酰胺的反式烯胺中间物的形成有深远影响。我们还表明,SA2-13 衍生物的设计有望对抗具有 K234R 取代的 IR SHV β-内酰胺酶。