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使用带有延迟提取的基质辅助激光解吸电离飞行时间质谱进行精确质量测量。

Accurate mass measurements using MALDI-TOF with delayed extraction.

作者信息

Takach E J, Hines W M, Patterson D H, Juhasz P, Falick A M, Vestal M L, Martin S A

机构信息

PerSeptive Biosystems, Inc., Framingham, Massachusetts 01701, USA.

出版信息

J Protein Chem. 1997 Jul;16(5):363-9. doi: 10.1023/a:1026376403468.

Abstract

Matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry is now an essential tool in biopolymer analysis. Sensitivity and mass range are unsurpassed, but mass measurement accuracy and resolution have been limited. With delayed extraction and a reflecting analyzer, mass measurements using MALDI-TOF can be made with an accuracy of a few parts per million (ppm). It is possible to distinguish Lys from Gln in peptides, and to determine the elemental composition of smaller molecules (mass 100-500). In database searching strategies, a smaller mass window, resulting from an increase in mass accuracy, greatly decreases the number of possible candidates. Mass measurement accuracy with errors less than 5 ppm is demonstrated on a mixture of 12 peptides ranging in mass from ca. 900 to 3700 Da. Mass measurements on 13 peaks in an unseparated tryptic digest of myoglobin gave results with an overall average error less than 3.5 ppm, with a maximum error of 7 ppm.

摘要

基质辅助激光解吸电离飞行时间(MALDI-TOF)质谱法如今是生物聚合物分析中的一项重要工具。其灵敏度和质量范围无与伦比,但质量测量精度和分辨率一直受到限制。采用延迟提取和反射式分析仪后,使用MALDI-TOF进行质量测量的精度可达百万分之几(ppm)。能够区分肽中的赖氨酸(Lys)和谷氨酰胺(Gln),并确定较小分子(质量为100 - 500)的元素组成。在数据库搜索策略中,质量精度提高导致质量窗口变小,极大地减少了可能的候选物数量。在质量约为900至3700 Da的12种肽的混合物上,展示了误差小于5 ppm的质量测量精度。对肌红蛋白未分离的胰蛋白酶消化产物中的13个峰进行质量测量,结果的总体平均误差小于3.5 ppm,最大误差为7 ppm。

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