Antimicrobial peptides: an alternative for innovative medicines?

被引:160
作者
da Costa, Joao Pinto [1 ]
Cova, Marta [1 ]
Ferreira, Rita [1 ]
Vitorino, Rui [1 ,2 ]
机构
[1] Univ Aveiro, Dept Chem, QOPNA, Mass Spectrometry Ctr, P-3810193 Aveiro, Portugal
[2] Univ Aveiro, Inst Res Biomed iBiMED, Hlth Sci Program, P-3810193 Aveiro, Portugal
关键词
Salivary peptide; Antitumoral; Synthesis; Bioinformatics; HOST-DEFENSE PEPTIDES; HISTIDINE-RICH POLYPEPTIDES; HUMAN CATHELICIDIN LL-37; UNNATURAL AMINO-ACIDS; SOLID-PHASE SYNTHESIS; ANTIBACTERIAL PEPTIDE; MAGNETIC NANOPARTICLES; SECONDARY STRUCTURE; ESCHERICHIA-COLI; WEB SERVER;
D O I
10.1007/s00253-015-6375-x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Antimicrobial peptides are small molecules with activity against bacteria, yeasts, fungi, viruses, bacteria, and even tumor cells that make these molecules attractive as therapeutic agents. Due to the alarming increase of antimicrobial resistance, interest in alternative antimicrobial agents has led to the exploitation of antimicrobial peptides, both synthetic and from natural sources. Thus, many peptide-based drugs are currently commercially available for the treatment of numerous ailments, such as hepatitis C, myeloma, skin infections, and diabetes. Initial barriers are being increasingly overcome with the development of cost-effective, more stable peptides. Herein, we review the available strategies for their synthesis, bioinformatics tools for the rational design of antimicrobial peptides with enhanced therapeutic indices, hurdles and shortcomings limiting the large-scale production of AMPs, as well as the challenges that the pharmaceutical industry faces on their use as therapeutic agents.
引用
收藏
页码:2023 / 2040
页数:18
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