Experimental concepts for linking the biological activities of antimicrobial peptides to their molecular modes of action

被引:30
|
作者
Malanovic, Nermina [1 ]
Marx, Lisa [1 ]
Blondelle, Sylvie E. [2 ]
Pabst, Georg [1 ]
Semeraro, Enrico F. [1 ]
机构
[1] Karl Franzens Univ Graz, Inst Mol Biosci, Biophys Div, Graz, Austria
[2] Sanford Burnham Prebys Med Discovery Inst, La Jolla, CA USA
来源
关键词
Antimicrobial peptides bacteria; Model systems; Membrane potential; Membrane fluidity; Membrane permeability; MIC; MBC; SAX/SANs; DSC; Zeta-potential; DIFFERENTIAL SCANNING CALORIMETRY; MEMBRANE-LIPID-COMPOSITION; GRAM-POSITIVE BACTERIAL; X-RAY-SCATTERING; SMALL-ANGLE; PHOSPHOLIPID-COMPOSITION; PSEUDOMONAS-AERUGINOSA; NEUTRON-SCATTERING; CELL ENVELOPES; MAGAININ;
D O I
10.1016/j.bbamem.2020.183275
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The search for novel compounds to combat multi-resistant bacterial infections includes exploring the potency of antimicrobial peptides and derivatives thereof. Complementary to high-throughput screening techniques, biophysical and biochemical studies of the biological activity of these compounds enable deep insight, which can be exploited in designing antimicrobial peptides with improved efficacy. This approach requires the combination of several techniques to study the effect of such peptides on both bacterial cells and simple mimics of their cell envelope, such as lipid-only vesicles. These efforts carry the challenge of bridging results across techniques and sample systems, including the proper choice of membrane mimics. This review describes some important concepts toward the development of potent antimicrobial peptides and how they translate to frequently applied experimental techniques, along with an outline of the biophysics pertaining to the killing mechanism of antimicrobial peptides.
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页数:14
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