Angel Peggi M, Norris-Caneda Kim, Drake Richard R
Department of Cell and Molecular Pharmacology & Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina.
Curr Protoc Protein Sci. 2018 Nov;94(1):e65. doi: 10.1002/cpps.65. Epub 2018 Aug 16.
Tryptic peptide imaging is a primary workflow for matrix-assisted laser desorption/ionization imaging mass spectrometry (MALDI IMS) and has led to new information reporting highly multiplexed protein localization. Technological advances within the last few years have produced robust tools for automated spraying of both matrix and enzymes. When combined with high-mass-resolution and high-mass-accuracy instrumentation, studies now generally result in two-dimensional mapping of well over 1,000 peptide peaks. This protocol describes sample preparation, spraying, and application of enzymes and matrices, and MALDI FT-ICR instrumental considerations for two-dimensional mapping of tryptic peptides from fresh-frozen or formalin-fixed, paraffin-embedded tissue sections. Procedures for extraction of tryptic peptides from tissue sections for LC-MS/MS identification are also described. © 2018 by John Wiley & Sons, Inc.
胰蛋白酶肽成像技术是基质辅助激光解吸/电离成像质谱(MALDI IMS)的主要工作流程,它带来了关于高度多重蛋白质定位的新信息报告。过去几年的技术进步产生了用于自动喷涂基质和酶的强大工具。当与高质量分辨率和高质量精度的仪器结合使用时,目前的研究通常会生成超过1000个肽峰的二维图谱。本方案描述了样品制备、喷涂以及酶和基质的应用,以及用于从新鲜冷冻或福尔马林固定、石蜡包埋组织切片中进行胰蛋白酶肽二维图谱分析的MALDI FT-ICR仪器注意事项。还描述了从组织切片中提取胰蛋白酶肽用于LC-MS/MS鉴定的程序。© 2018约翰威立父子出版公司版权所有