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Illuminating the lipidome to advance biomedical research: peptide-based probes of membrane lipids

机译:照亮脂质组以推进生物医学研究:基于肽的膜脂质探针

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摘要

Systematic investigation of the lipidome will reveal new opportunities for disease diagnosis and intervention. However, lipidomic research has been hampered by the lack of molecular tools to track specific lipids of interest. Accumulating reports indicate lipid recognition can be achieved with properly constructed short peptides in addition to large proteins. This review summarizes the key developments of this area within the past decade. Select lantibiotic peptides present the best examples of low-molecular-weight probes of membrane lipids, displaying selectivity comparable to lipid-binding proteins. Designed peptides, through biomimetic approaches and combinational screening, have begun to demonstrate their potential for lipid tracking in cultured cells and even in living organisms. Biophysical characterization of these lipid-targeting peptides has revealed certain features critical for selective membrane binding, including preorganized scaffolds and the balance of polar and nonpolar interactions. The knowledge summarized herein should facilitate the development of molecular tools to target a variety of membrane lipids.
机译:对脂质组的系统研究将揭示疾病诊断和干预的新机会。但是,由于缺乏追踪特定目标脂质的分子工具,脂质组学研究受到阻碍。越来越多的报告表明,除了大蛋白之外,还可以通过适当构建的短肽来实现脂质识别。这篇综述总结了过去十年该领域的主要发展。精选羊毛硫抗生素肽是膜脂质低分子量探针的最佳实例,其选择性可与脂质结合蛋白媲美。通过仿生方法和组合筛选设计的肽已开始证明其在培养细胞甚至活生物体中进行脂质追踪的潜力。这些靶向脂质的肽的生物物理特性揭示了某些对选择性膜结合至关重要的特征,包括预组织的支架以及极性和非极性相互作用的平衡。本文总结的知识应有助于开发针对各种膜脂的分子工具。

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