Literature DB >> 21964792

Protein identification by MALDI-TOF mass spectrometry.

Judith Webster1, David Oxley.   

Abstract

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.

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Year:  2012        PMID: 21964792     DOI: 10.1007/978-1-61779-349-3_15

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  19 in total

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Journal:  BMC Med Genomics       Date:  2014-12-24       Impact factor: 3.063

9.  MALDI-TOF MS and CD spectral analysis for identification and structure prediction of a purified, novel, organic solvent stable, fibrinolytic metalloprotease from Bacillus cereus B80.

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10.  Quantitative Proteomic Analysis of Differentially Expressed Protein Profiles Involved in Pancreatic Ductal Adenocarcinoma.

Authors:  Kung-Kai Kuo; Chao-Jen Kuo; Chiang-Yen Chiu; Shih-Shin Liang; Chun-Hao Huang; Shu-Wen Chi; Kun-Bow Tsai; Chiao-Yun Chen; Edward Hsi; Kuang-Hung Cheng; Shyh-Horng Chiou
Journal:  Pancreas       Date:  2016-01       Impact factor: 3.327

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