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评估一种用于基质辅助激光解吸/电离飞行时间质谱的靶向样品制备系统,该系统与常规流动肽高效液相色谱联用进行肽质量指纹分析。

Evaluation of an on-target sample preparation system for matrix-assisted laser desorption/ionization time-of-flight mass spectrometry in conjunction with normal-flow peptide high-performance liquid chromatography for peptide mass fingerprint analyses.

作者信息

McComb Mark E, Perlman David H, Huang Hua, Costello Catherine E

机构信息

Cardiovascular Proteomics Center, Boston University School of Medicine, Boston, MA 02118-2646, USA.

出版信息

Rapid Commun Mass Spectrom. 2007;21(1):44-58. doi: 10.1002/rcm.2805.

Abstract

Large-scale mass spectrometry (MS)-based proteomic analyses require high-throughput sample preparation techniques due to the increasing numbers of samples that make up a typical proteomics experiment. Moreover, extensive sample pre-treatment steps are necessary prior to MS acquisition for even the most rapid and robust MS-based proteomics methodology, matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) MS followed by peptide mass fingerprinting (PMF) analysis. These include sample purification and fractionation, removal of digestion buffers or solvents, and spotting of sample with matrix onto the MALDI target. These multiple steps of time-consuming sample handling can result in high overall analysis costs and the likelihood of sample contamination and loss. In order to overcome some of these limitations in sample processing, we have investigated the use of a novel, simple, inexpensive 96-well elastomeric array that affixes to a MALDI target to create an on-target 96-well plate that accommodates a high solution volume (ca. 200 microL), thereby enabling the on-target processing of samples for MALDI-TOFMS. We explored several factors that influence MALDI sample preparation: type of matrix, solution volume, solution organic composition, solution drying rates and matrix/analyte co-crystallization methods. We also investigated the use of the 96-well elastomeric device for coupling MALDI-TOFMS analysis directly to high flow rate (1 mL/min) reversed-phase (rp)-HPLC. By developing an optimized, robust sample preparation protocol, we were able to obtain mass spectra with a high signal-to-noise ratio from peptide standards present at the 50-fmol level in large starting volumes of solution. PMF analyses were possible from 1-pmol and 500-fmol protein-digest standards. Coupling the device to high-flow HPLC (750 microL/min) yielded a robust and semi-automated means to obtain enhanced MALDI-TOFMS data at 500 ng of protein digest. These methodologies developed for this simple, on-target, elastomeric device show promise for streamlining the sample preparation process from HPLC to MALDI-MS.

摘要

由于构成典型蛋白质组学实验的样本数量不断增加,基于大规模质谱(MS)的蛋白质组学分析需要高通量样本制备技术。此外,即使是最快速、最强大的基于MS的蛋白质组学方法,即基质辅助激光解吸/电离飞行时间(MALDI-TOF)MS随后进行肽质量指纹图谱(PMF)分析,在进行MS采集之前也需要进行广泛的样本预处理步骤。这些步骤包括样本纯化和分级分离、去除消化缓冲液或溶剂,以及将样本与基质点样到MALDI靶板上。这些耗时的样本处理多个步骤可能导致总体分析成本高昂,以及样本污染和损失的可能性。为了克服样本处理中的一些这些限制,我们研究了一种新型、简单、廉价的96孔弹性体阵列的使用,该阵列固定在MALDI靶板上,以创建一个容纳高溶液体积(约200微升)的靶上96孔板,从而能够对用于MALDI-TOFMS的样本进行靶上处理。我们探索了几个影响MALDI样本制备的因素:基质类型、溶液体积、溶液有机组成、溶液干燥速率和基质/分析物共结晶方法。我们还研究了使用96孔弹性体装置将MALDI-TOFMS分析直接与高流速(1毫升/分钟)反相(rp)-HPLC联用。通过开发一种优化、稳健的样本制备方案,我们能够从大量起始溶液体积中50飞摩尔水平的肽标准品获得具有高信噪比的质谱图。从1皮摩尔和500飞摩尔蛋白质消化标准品进行PMF分析是可行的。将该装置与高流速HPLC(750微升/分钟)联用,产生了一种稳健的半自动方法,以在500纳克蛋白质消化物时获得增强的MALDI-TOFMS数据。为这种简单的靶上弹性体装置开发的这些方法显示出有望简化从HPLC到MALDI-MS的样本制备过程。

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