Madani Fatemeh, Gräslund Astrid
Department of Clinical Neuroscience, Center for Molecular Medicine (CMM), Karolinska Institutet, 17176, Stockholm, Sweden,
Methods Mol Biol. 2015;1324:73-87. doi: 10.1007/978-1-4939-2806-4_5.
Despite many studies made on cell-penetrating peptides (CPPs), the mechanism of their cellular uptake and endosomal escape has not been completely resolved. This is even more unclear when the CPP is bound either covalently or non-covalently to the cargo molecules. To answer remaining questions, we require a combination of different methods, model systems, and experiments since there is no single method which could give a complete answer to all questions. Biophysical investigations of CPPs have a significant impact on CPP research considering their molecular mechanisms of action. In this chapter, we present different membrane model systems suitable for biophysical studies as well as the basic practical aspects underlying several common biophysical methods and experiments. The methods include fluorescence spectroscopy, circular dichroism spectroscopy, and dynamic light scattering and concern peptide-membrane interactions and vesicle model membrane leakage. We have also described the potential and limitations of biophysical studies on the CPP-membrane interactions and their impact on our understanding of how CPPs mediate the transport of cargoes into living cells.
尽管对细胞穿透肽(CPPs)进行了许多研究,但其细胞摄取和内体逃逸的机制尚未完全解决。当CPP与货物分子共价或非共价结合时,情况就更不清楚了。为了回答剩下的问题,我们需要结合不同的方法、模型系统和实验,因为没有一种单一的方法能够对所有问题给出完整的答案。考虑到CPP的分子作用机制,对其进行生物物理研究对CPP研究有重大影响。在本章中,我们介绍了适用于生物物理研究的不同膜模型系统,以及几种常见生物物理方法和实验背后的基本实践方面。这些方法包括荧光光谱法、圆二色光谱法和动态光散射法,涉及肽-膜相互作用和囊泡模型膜泄漏。我们还描述了CPP-膜相互作用生物物理研究的潜力和局限性,以及它们对我们理解CPP如何介导货物转运到活细胞中的影响。