Literature DB >> 8481542

In situ reduction suitable for matrix-assisted laser desorption/ionization and liquid secondary ionization using tris(2-carboxyethyl)phosphine.

W H Fischer1, J E Rivier, A G Craig.   

Abstract

The suitability of the hydrochloride salt of tris(2-carboxyethyl)phosphine (TCEP) for in situ reduction with matrix-assisted laser desorption/ionization (MALDI) and liquid secondary ionization (LSI) mass spectrometry is evaluated. TCEP can be used to irreversibly reduce organic disulfides to thiols in water and is active at an acidic pH. We found that TCEP was suitable for partial reduction of bovine insulin deposited on the target and mixed with either sinapinic acid in MALDI or glycerol and m-nitrobenzyl alcohol in LSIMS. When TCEP was added to insulin deposited on the target without prior mixing of sinapinic acid the in situ MALDI protocol resulted in almost complete reduction.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8481542     DOI: 10.1002/rcm.1290070312

Source DB:  PubMed          Journal:  Rapid Commun Mass Spectrom        ISSN: 0951-4198            Impact factor:   2.419


  2 in total

1.  A tris (2-carboxyethyl) phosphine (TCEP) related cleavage on cysteine-containing proteins.

Authors:  Peiran Liu; Brian W O'Mara; Bethanne M Warrack; Wei Wu; Yunping Huang; Yihong Zhang; Rulin Zhao; Mei Lin; Michael S Ackerman; Peter K Hocknell; Guodong Chen; Li Tao; Siegfried Rieble; Jack Wang; David B Wang-Iverson; Adrienne A Tymiak; Michael J Grace; Reb J Russell
Journal:  J Am Soc Mass Spectrom       Date:  2010-01-28       Impact factor: 3.109

2.  Disulfide structures of highly bridged peptides: a new strategy for analysis.

Authors:  W R Gray
Journal:  Protein Sci       Date:  1993-10       Impact factor: 6.725

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.