Advancements in peptide-based antimicrobials: A possible option for emerging drug-resistant infections

被引:3
|
作者
Yadav, Nitin [2 ,3 ]
Chauhan, Virander S. [1 ,2 ,3 ]
机构
[1] Gandhi Inst Technol & Management, Visakhapatnam 530045, Andhra Pradesh, India
[2] Int Ctr Genet Engn & Biotechnol, Mol Med, Aruna Asaf Ali Marg, New Delhi 110067, India
[3] Biotide Solut LLP, B-23 Geetanjali Enclave, New Delhi 110017, India
关键词
Antimicrobial peptides (AMPs); Multi-drug resistance; Synthetic peptides; Mechanism of action of AMPs; Novel antimicrobial agents; Peptide therapeutics; ANTIBACTERIAL PEPTIDE; MOLECULAR-MECHANISM; SECONDARY STRUCTURE; SYNTHETIC PEPTIDES; NISIN RESISTANCE; LACTOFERRICIN B; MAGAININ; MEMBRANE; BACTERIAL; PROTEIN;
D O I
10.1016/j.cis.2024.103282
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In recent years, multidrug-resistant pathogenic microorganisms (MDROs) have emerged as a severe threat to human health, exhibiting robust resistance to traditional antibiotics. This has created a formidable challenge in modern medicine as we grapple with limited options to combat these resilient bacteria. Despite extensive efforts by scientists to develop new antibiotics targeting these pathogens, the quest for novel antibacterial molecules has become increasingly arduous. Fortunately, nature offers a potential solution in the form of cationic antimicrobial peptides (AMPs) and their synthetic counterparts. AMPs, naturally occurring peptides, have displayed promising efficacy in fighting bacterial infections by disrupting bacterial cell membranes, hindering their survival and reproduction. These peptides, along with their synthetic mimics, present an exciting alternative in combating antibiotic resistance. They hold the potential to emerge as a formidable tool against MDROs, offering hope for improved strategies to protect communities. Extensive research has explored the diversity, history, and structureproperties relationship of AMPs, investigating their amphiphilic nature for membrane disruption and mechanisms of action. However, despite their therapeutic promise, AMPs face several documented limitations. Among these challenges, poor pharmacokinetic properties stand out, impeding the attainment of therapeutic levels in the body. Additionally, some AMPs exhibit toxicity and susceptibility to protease cleavage, leading to a short half-life and reduced efficacy in animal models. These limitations pose obstacles in developing effective treatments based on AMPs. Furthermore, the high manufacturing costs associated with AMPs could significantly hinder their widespread use. In this review, we aim to present experimental and theoretical insights into different AMPs, focusing specifically on antibacterial peptides (ABPs). Our goal is to offer a concise overview of peptide-based drug candidates, drawing from a wide array of literature and peer-reviewed studies. We also explore recent advancements in AMP development and discuss the challenges researchers face in moving these molecules towards clinical trials. Our main objective is to offer a comprehensive overview of current AMP and ABP research to guide the development of more precise and effective therapies for bacterial infections.
引用
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页数:17
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