What can light scattering spectroscopy do for membrane-active peptide studies

被引:72
作者
Domingues, Marco M. [1 ]
Santiago, Patricia S. [2 ]
Castanho, Miguel A. R. B. [1 ]
Santos, Nuno C. [1 ]
机构
[1] Univ Lisbon, Fac Med, Unidade Biomembranas, Inst Mol Med, P-1649028 Lisbon, Portugal
[2] Univ Sao Paulo, Inst Quim Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil
关键词
dynamic light scattering; static light scattering; zeta-potential; therapeutic peptides;
D O I
10.1002/psc.1007
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
Highly charged peptides are important components of the immune system and belong to an important family of antibiotics. Although their therapeutic activity is known, most of the molecular level mechanisms are controversial. A wide variety of different approaches are usually applied to understand their mechanisms, but light scattering techniques are frequently overlooked. Yet, light scattering is a noninvasive technique that allows insights both on the peptide mechanism of action as well as on the development of new antibiotics. Dynamic light scattering (DLS) and static light scattering (SLS) are used to measure the aggregation process of lipid vesicles upon addition of peptides and molecular properties (shape, molecular weight). The high charge of these peptides allows electrostatic attraction toward charged lipid vesicles, which is studied by zeta potential (zeta-potential) measurements. Copyright (c) 2008 European Peptide Society and John Wiley & Sons, Ltd.
引用
收藏
页码:394 / 400
页数:7
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