Literature DB >> 21948412

Quantifying attomole amounts of proteins from complex samples by nano-LC and selected reaction monitoring.

Thomas Fröhlich1, Georg J Arnold.   

Abstract

Selected reaction monitoring (SRM) is one of the most powerful techniques for the relative and absolute quantification of proteins from complex protein mixtures. In contrast to traditional protein quantification methods such as ELISAs or RIAs, the SRM method uses mass spectrometry for detection. Further benefits of SRM are as follows: (1) high specificity and sensitivity; (2) large linear dynamic range of at least three orders of magnitude; and (3) the possibility to quantify multiple proteins simultaneously in a single MS run from an individual sample. To perform SRM-based protein quantification reliably, a careful design of the assay is essential, and several pitfalls must be avoided. The aim of this chapter is to help SRM newcomers to establish SRM-based protein quantification assays and discuss an overview of typical work flows that are applied during SRM assay development.

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Year:  2011        PMID: 21948412     DOI: 10.1007/978-1-61779-319-6_11

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


  3 in total

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Journal:  Anal Chem       Date:  2012-08-21       Impact factor: 6.986

Review 2.  Parallel Reaction Monitoring: A Targeted Experiment Performed Using High Resolution and High Mass Accuracy Mass Spectrometry.

Authors:  Navin Rauniyar
Journal:  Int J Mol Sci       Date:  2015-12-02       Impact factor: 5.923

3.  Postovulatory aging affects dynamics of mRNA, expression and localization of maternal effect proteins, spindle integrity and pericentromeric proteins in mouse oocytes.

Authors:  T Trapphoff; M Heiligentag; D Dankert; H Demond; D Deutsch; T Fröhlich; G J Arnold; R Grümmer; B Horsthemke; U Eichenlaub-Ritter
Journal:  Hum Reprod       Date:  2015-11-17       Impact factor: 6.918

  3 in total

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