Antimicrobial Peptides and Their Assemblies

被引:2
|
作者
Carmona-Ribeiro, Ana Maria [1 ]
机构
[1] Sao Paulo State Univ, Chem Inst, Biochem Dept, Biocolloids Lab, Ave Prof Lineu Prestes 748, BR-05508000 Sao Paulo, Sao Paulo, Brazil
来源
FUTURE PHARMACOLOGY | 2023年 / 3卷 / 04期
关键词
AMPs approved in the clinic; AMP degradation and toxicity; mechanisms of action; AMP self-assemblies; AMPs combined with other antimicrobials; AMP delivery; MEMBRANE INTERACTIONS; BIOMEDICAL APPLICATIONS; VANCOMYCIN RESISTANCE; GRAMICIDIN-A; POLYMYXIN-B; MECHANISM; DELIVERY; ION; LIPOPOLYSACCHARIDE; NANOPARTICLES;
D O I
10.3390/futurepharmacol3040047
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Antibiotic resistance requires alternatives to fight multi-drug resistant strains. Antimicrobial peptides (AMPs) act by disrupting or solubilizing microbial cell walls or membranes in accordance with mechanisms difficult to counteract from the microbe's point of view. In this review, structure-activity relationships for AMPs and their assemblies are discussed, considering not only their self-assembly but also their interactions with their carriers for optimal delivery or their combinations with other complementary antimicrobials or moieties covalently bound to their chemical structure. The effect of the formulations on AMP activity is also evaluated, revealing a myriad of possibilities. Depending on the interaction forces between the AMP, the carrier, or the elements added to the formulations, AMP activity can be reduced, enhanced, or remain unaffected. Approaches protecting AMPs against proteolysis may also reduce their activity.
引用
收藏
页码:763 / 788
页数:26
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