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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >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
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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

机译:用于基质辅助激光解吸/电离飞行时间质谱联用的正常流动肽高效液相色谱法进行肽质量指纹分析的目标样品制备系统的评估

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摘要

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 mu L), 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 mu L/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. Copyright (c) 2006 John Wiley & Sons, Ltd.
机译:基于大规模质谱(MS)的蛋白质组学分析需要高通量的样品制备技术,因为构成典型蛋白质组学实验的样品数量不断增加。此外,即使是最快速,最可靠的基于MS的蛋白质组学方法,基质辅助激光解吸/电离飞行时间(MALDI-TOF)MS以及随后的肽质量指纹图谱分析,MS采集之前也必须进行大量的样品预处理步骤(PMF)分析。这些措施包括样品纯化和分离,去除消化缓冲液或溶剂,以及将带有基质的样品点样到MALDI目标物上。耗时的样品处理的这些多个步骤会导致较高的总体分析成本以及样品污染和损失的可能性。为了克服样品处理中的某些局限性,我们研究了使用新颖,简单,廉价的96孔弹性体阵列,该阵列固定在MALDI靶标上,以创建可容纳高浓度溶液的靶上96孔板体积(约200μL),从而能够按目标处理MALDI-TOFMS样品。我们探讨了影响MALDI样品制备的几个因素: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孔弹性体设备将MALDI-TOFMS分析直接耦合至高流速(1 mL / min)反相(rp)-HPLC的方法。通过开发优化的,稳健的样品前处理方案,我们能够从较大起始体积的溶液中以50-fmol浓度存在的肽标准物中获得具有高信噪比的质谱图。 PMF分析可以从1 pmol和500 fmol的蛋白质消化标准物中进行。将设备与高流量HPLC(750μL / min)耦合产生了一种强大且半自动化的方法,可以在500 ng蛋白质消化物中获得增强的MALDI-TOFMS数据。为这种简单的,针对性的,弹性体设备开发的这些方法论显示出有望简化从HPLC到MALDI-MS的样品制备过程。版权所有(c)2006 John Wiley&Sons,Ltd.

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