Protein Identification by MALDI-TOF Mass Spectrometry
Judith Webster, David Oxley
Babraham Institute
阅读操作
确认中在文库中上传 PDF 后可生成中文音频讲解。
摘要与影响
MALDI-TOF mass spectrometers are now commonplace and their relative ease of use means that most non-specialist labs can readily access the technology for the rapid and sensitive analysis of biomolecules. One of the main uses of MALDI-TOF-MS is in the identification of proteins, by peptide mass fingerprinting (PMF). Here we describe a simple protocol that can be performed in a standard biochemistry laboratory, whereby proteins separated by 1D or 2D gel electrophoresis can be identified at femtomole levels. The procedure involves excision of the spot or band from the gel, washing and destaining, reduction and alkylation, in-gel trypsin digestion, MALDI-TOF-MS of the tryptic peptides and database searching of the PMF data. Up to 96 protein samples can easily be manually processed at one time by this method.
逐年被引趋势
关键指标
同类平均 = 1
同领域 · 同年份 · 同类型
Google Scholar 与 OpenAlex 的被引统计范围不同,数值存在差异属正常。
AI 辅助阅读
依据:摘要
可就本文提问;依据不足时会说明。
学术脉络
学科主题
化学Mass Spectrometry Techniques and Applications
Advanced Proteomics Techniques and Applications · Metabolomics and Mass Spectrometry Studies
参考文献 9
此处列出前 3 条
引用本文 73
按被引量排序,此处列出前 3 条