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CZE-ESI-MS/MS 系统,用于分析细胞匀浆的胰蛋白酶消化物的亚纳克数量。

CZE-ESI-MS/MS system for analysis of subnanogram amounts of tryptic digests of a cellular homogenate.

机构信息

Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556, USA.

出版信息

Proteomics. 2012 Oct;12(19-20):3013-9. doi: 10.1002/pmic.201200100. Epub 2012 Aug 29.

Abstract

We report the performance of capillary zone electrophoresis coupled with an electrokinetically pumped electrospray interface and an Orbitrap-Velos mass spectrometer for high sensitivity protein analysis. We first investigated the system for quantitation of the tryptic digest of BSA. The system produced outstanding linearity with respect to peak height, number of peptide IDs, and spectral counts across the range of 12 nM to 750 nM (60 amol to 3.5 fmol) of BSA injected. One peptide produced a detection limit of 0.3 nM (1.5 amol) injected. We also analyzed 700 pg of a tryptic digest prepared from a RAW264.7 cell lysate; ten proteins were identified in triplicate analyses after filtering the data with peptide confidence value as high. This sample size corresponds to the protein content of approximately ten eukaryotic cells.

摘要

我们报告了毛细管区带电泳与电动泵电喷雾接口和轨道阱 Velos 质谱联用用于高灵敏度蛋白质分析的性能。我们首先研究了该系统用于定量分析 BSA 的胰蛋白酶消化物。该系统在注射的 BSA 浓度范围为 12 nM 至 750 nM(60 amol 至 3.5 fmol)时,在峰高、肽 ID 数量和谱图计数方面表现出出色的线性关系。一种肽的检出限为 0.3 nM(1.5 amol)。我们还分析了从 RAW264.7 细胞裂解物制备的 700 pg 胰蛋白酶消化物;在用肽置信值高的方法过滤数据后,在重复分析中鉴定了十种蛋白质。该样品量相当于大约十个真核细胞的蛋白质含量。

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