Li Jianguo, Koh Jun-Jie, Liu Shouping, Lakshminarayanan Rajamani, Verma Chandra S, Beuerman Roger W
Ocular Chemistry and Anti-Infectives, Singapore Eye Research InstituteSingapore, Singapore; Agency for Science, Technology and Research (ASTAR), Bioinformatics InstituteSingapore, Singapore; Duke-NUS Graduate Medical School, SRP Neuroscience and BDSingapore, Singapore.
Ocular Chemistry and Anti-Infectives, Singapore Eye Research Institute Singapore, Singapore.
Front Neurosci. 2017 Feb 14;11:73. doi: 10.3389/fnins.2017.00073. eCollection 2017.
Antimicrobial peptides (AMPs) are promising next generation antibiotics that hold great potential for combating bacterial resistance. AMPs can be both bacteriostatic and bactericidal, induce rapid killing and display a lower propensity to develop resistance than do conventional antibiotics. Despite significant progress in the past 30 years, no peptide antibiotic has reached the clinic yet. Poor understanding of the action mechanisms and lack of rational design principles have been the two major obstacles that have slowed progress. Technological developments are now enabling multidisciplinary approaches including molecular dynamics simulations combined with biophysics and microbiology toward providing valuable insights into the interactions of AMPs with membranes at atomic level. This has led to increasingly robust models of the mechanisms of action of AMPs and has begun to contribute meaningfully toward the discovery of new AMPs. This review discusses the detailed action mechanisms that have been put forward, with detailed atomistic insights into how the AMPs interact with bacterial membranes. The review further discusses how this knowledge is exploited toward developing design principles for novel AMPs. Finally, the current status, associated challenges, and future directions for the development of AMP therapeutics are discussed.
抗菌肽(AMPs)是很有前景的下一代抗生素,在对抗细菌耐药性方面具有巨大潜力。抗菌肽兼具抑菌和杀菌作用,能迅速杀灭细菌,且与传统抗生素相比,产生耐药性的倾向较低。尽管在过去30年里取得了重大进展,但尚无肽类抗生素进入临床。对作用机制的理解不足和缺乏合理的设计原则是阻碍进展的两大主要障碍。目前的技术发展使得多学科方法成为可能,包括结合生物物理学和微生物学的分子动力学模拟,以便在原子水平上深入了解抗菌肽与膜的相互作用。这已产生了越来越完善的抗菌肽作用机制模型,并开始为发现新的抗菌肽做出有意义的贡献。本综述讨论了已提出的详细作用机制,并对抗菌肽如何与细菌膜相互作用进行了详细的原子层面分析。该综述还进一步讨论了如何利用这些知识来制定新型抗菌肽的设计原则。最后,讨论了抗菌肽疗法的现状、相关挑战及未来发展方向。