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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Matrix-assisted laser desorption/ionization directed nano-electrospray ionization tandem mass spectrometric analysis for protein identification
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Matrix-assisted laser desorption/ionization directed nano-electrospray ionization tandem mass spectrometric analysis for protein identification

机译:基质辅助激光解吸/电离定向纳米电喷雾串联质谱用于蛋白质鉴定

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In those cases where the information obtained by peptide mass fingerprinting or matrix-assisted laser desorption/ionization tandem mass spectrometry (MALDI-MS/MS) is not sufficient for unambiguous protein identification, nano-electrospray ionization (nano-ESI) and/or electrospray ionization tandem mass spectrometry (ESI-MS/MS) analysis must be performed. The sensitivity of nano-ESI/MS, however, is lower than that of MALDI-MS, especially at very low analyte concentrations and/or in the presence of contaminants, such as salt and detergents. Moreover, to perform ESI-MS/ MS, the peptide masses of the precursor ions must be known. The approach described in this paper, MALDI-directed nano-ESI-MS/MS, makes use of information obtained from the more sensitive MALDI-MS experiments in order to direct subsequent nano-ESI-MS/MS experiments. Peptide molecular ions found in the MALDI-MS analysis are then selected, as their (+2) precursor ions, for nano-ESI-MS/MS sequencing, even though these ions cannot be detected in the ESI-MS spectra. This method, originally proposed by Tempst et al.(Anal. Chem. 2000, 72: 777-790), has been extended to provide better sensitivity and shorter analysis times; also, a comparison with liquid chromatography/tandem mass spectrometry (LC/MS/MS) has been performed. These experiments, performed using quadrupole time-of-flight instruments equipped with commercially available nano-ESI sources, have allowed the unambiguous identification of in-gel digested proteins at levels below their ESI-MS detection limits, even in the presence of salts and detergents. Copyright (C) 2003 John Wiley Sons, Ltd. [References: 30]
机译:在那些通过肽质谱指纹图谱或基质辅助激光解吸/电离串联质谱(MALDI-MS / MS)获得的信息不足以明确识别蛋白质的情况下,需进行纳米电喷雾电离(nano-ESI)和/或电喷雾必须执行电离串联质谱分析(ESI-MS / MS)。但是,纳米ESI / MS的灵敏度低于MALDI-MS,尤其是在分析物浓度非常低和/或存在盐和去污剂等污染物的情况下。而且,要执行ESI-MS / MS,必须知道前体离子的肽质量。本文描述的方法是MALDI指导的nano-ESI-MS / MS,它利用从更敏感的MALDI-MS实验中获得的信息来指导后续的nano-ESI-MS / MS / MS实验。然后,选择MALDI-MS分析中发现的肽分子离子作为其(+2)前体离子,以进行纳米ESI-MS / MS测序,即使这些离子无法在ESI-MS光谱中检测到。该方法最初由Tempst等人提出(Anal。Chem。2000,72:777-790),现已得到扩展,以提供更好的灵敏度和更短的分析时间。另外,还与液相色谱/串联质谱法(LC / MS / MS)进行了比较。这些实验是使用装有市售纳米ESI离子源的四极飞行时间仪器进行的,即使在存在盐和去污剂的情况下,也可以明确鉴定低于ESI-MS检测限的凝胶消化蛋白质。 。版权所有(C)2003 John Wiley Sons,Ltd. [引用:30]

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