Suppr超能文献

使用新鲜冷冻或福尔马林固定、石蜡包埋组织通过基质辅助激光解吸电离成像质谱对胰蛋白酶肽进行原位成像

In Situ Imaging of Tryptic Peptides by MALDI Imaging Mass Spectrometry Using Fresh-Frozen or Formalin-Fixed, Paraffin-Embedded Tissue.

作者信息

Angel Peggi M, Norris-Caneda Kim, Drake Richard R

机构信息

Department of Cell and Molecular Pharmacology & Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina.

出版信息

Curr Protoc Protein Sci. 2018 Nov;94(1):e65. doi: 10.1002/cpps.65. Epub 2018 Aug 16.

Abstract

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.

摘要

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

相似文献

引用本文的文献

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验