Laboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University, 1230 York Avenue, New York, New York 10065, USA.
Acc Chem Res. 2011 Sep 20;44(9):699-708. doi: 10.1021/ar200063v. Epub 2011 Jun 15.
Protein lipidation and lipid trafficking control many key biological functions in all kingdoms of life. The discovery of diverse lipid species and their covalent attachment to many proteins has revealed a complex and regulated network of membranes and lipidated proteins that are central to fundamental aspects of physiology and human disease. Given the complexity of lipid trafficking and the protein targeting mechanisms involved with membrane lipids, precise and sensitive methods are needed to monitor and identify these hydrophobic molecules in bacteria, yeast, and higher eukaryotes. Although many analytical methods have been developed for characterizing membrane lipids and covalently modified proteins, traditional reagents and approaches have limited sensitivity, do not faithfully report on the lipids of interest, or are not readily accessible. The invention of bioorthogonal ligation reactions, such as the Staudinger ligation and azide-alkyne cycloadditions, has provided new tools to address these limitations, and their use has begun to yield fresh insight into the biology of protein lipidation and lipid trafficking. In this Account, we discuss how these new bioorthogonal ligation reactions and lipid chemical reporters afford new opportunities for exploring the biology of lipid-modified proteins and lipid trafficking. Lipid chemical reporters from our laboratory and several other research groups have enabled improved detection and large-scale proteomic analysis of fatty-acylated and prenylated proteins. For example, fatty acid and isoprenoid chemical reporters in conjunction with bioorthogonal ligation methods have circumvented the limited sensitivity and hazards of radioactive analogues, allowing rapid and robust fluorescent detection of lipidated proteins in all organisms tested. These chemical tools have revealed alterations in protein lipidation in different cellular states and are beginning to provide unique insights in mechanisms of regulation. Notably, the purification of proteins labeled with lipid chemical reporters has allowed both the large-scale analysis of lipidated proteins as well as the discovery of new lipidated proteins involved in metabolism, gene expression, and innate immunity. Specific lipid reporters have also been developed to monitor the trafficking of soluble lipids; these species are enabling bioorthogonal imaging of membranes in cells and tissues. Future advances in bioorthogonal chemistry, specific lipid reporters, and spectroscopy should provide important new insight into the functional roles of lipidated proteins and membranes in biology.
蛋白质脂质化和脂质运输控制着所有生命领域的许多关键生物学功能。不同脂质种类的发现及其与许多蛋白质的共价连接揭示了一个复杂而受调控的膜和脂质化蛋白质网络,这些是生理学和人类疾病的基本方面的核心。鉴于脂质运输的复杂性以及涉及膜脂的蛋白质靶向机制,需要精确和敏感的方法来监测和鉴定细菌、酵母和高等真核生物中的这些疏水分子。尽管已经开发了许多用于表征膜脂和共价修饰蛋白质的分析方法,但传统试剂和方法的灵敏度有限,不能真实地报告感兴趣的脂质,或者不易获得。生物正交连接反应的发明,如 Staudinger 连接和叠氮-炔环加成反应,为解决这些限制提供了新的工具,并且它们的使用已经开始为蛋白质脂质化和脂质运输的生物学提供新的见解。在本报告中,我们讨论了这些新的生物正交连接反应和脂质化学报告器如何为探索脂质修饰蛋白质和脂质运输的生物学提供新的机会。我们实验室和其他几个研究小组的脂质化学报告器使脂肪酸酰化和异戊二烯基化蛋白质的改进检测和大规模蛋白质组学分析成为可能。例如,与生物正交连接方法结合使用的脂肪酸和异戊二烯化学报告器避免了放射性类似物的有限灵敏度和危害,允许在所有测试的生物体中快速而稳健地荧光检测脂质化蛋白质。这些化学工具揭示了不同细胞状态下蛋白质脂质化的改变,并开始为调节机制提供独特的见解。值得注意的是,用脂质化学报告器标记的蛋白质的纯化不仅允许对脂质化蛋白质进行大规模分析,还允许发现涉及代谢、基因表达和先天免疫的新的脂质化蛋白质。还开发了特定的脂质报告器来监测可溶性脂质的运输;这些物质正在实现细胞和组织中膜的生物正交成像。生物正交化学、特定脂质报告器和光谱学的未来进展应该为脂质化蛋白质和膜在生物学中的功能作用提供重要的新见解。