Department of Biology and Center for Microbial Sciences, San Diego State University, San Diego, CA 92182, USA.
Peptides. 2013 Feb;40:112-22. doi: 10.1016/j.peptides.2012.12.025. Epub 2013 Jan 3.
DNA repair pathways in bacteria that use homologous recombination involve the formation and subsequent resolution of Holliday junction (HJ) intermediates. We have previously identified several hexameric peptides that bind to HJs and interfere with HJ processing enzymes in vitro. The peptide WRWYCR and its D-amino acid stereoisomer wrwycr, are potent antibacterial agents. These hexapeptides must form homodimers in order to interact stably with HJs, and inhibit bacterial growth, and this represents a potential limitation. Herein we describe a disulfide bond-independent inhibitor, WRWYRGGRYWRW and its D-stereoisomer wrwyrggrywrw. We have characterized these single-chain, linear analogs of the hexapeptides, and show that in addition to effectively binding to HJs, and inhibiting the activity of DNA repair enzymes that process HJs, they have equal or greater potency against Gram-positive and Gram-negative bacterial growth. The analogs were also shown to cause DNA damage in bacteria, and disrupt the integrity of the bacterial cytoplasmic membrane. Finally, we found that they have little toxicity toward several eukaryotic cell types at concentrations needed to inhibit bacterial growth.
细菌中利用同源重组的 DNA 修复途径涉及 Holliday 连接(HJ)中间体的形成和随后的解决。我们之前已经鉴定出几种六聚体肽,它们与 HJ 结合,并在体外干扰 HJ 加工酶。六肽 WRWYCR 及其 D-氨基酸立体异构体 wrwycr 是有效的抗菌剂。这些六肽必须形成同源二聚体才能与 HJ 稳定相互作用,并抑制细菌生长,这是一个潜在的限制。本文中,我们描述了一种不依赖二硫键的抑制剂 WRWYRGGRYWRW 及其 D-立体异构体 wrwyrggrywrw。我们已经对这些六肽的单链线性类似物进行了表征,并表明除了有效地与 HJ 结合并抑制处理 HJ 的 DNA 修复酶的活性外,它们对革兰氏阳性和革兰氏阴性细菌的生长具有同等或更高的效力。这些类似物还被证明会在细菌中引起 DNA 损伤,并破坏细菌细胞质膜的完整性。最后,我们发现它们在抑制细菌生长所需的浓度下对几种真核细胞类型的毒性很小。