Literature DB >> 2425658

Peptide sequence analysis using exopeptidases with molecular analysis of the truncated polypeptides by mass spectrometry.

R M Caprioli, T Fan.   

Abstract

Fast atom bombardment mass spectrometry is used for the analysis of the series of molecular products formed by the cleavage of polypeptide substrates with the exopeptidases carboxypeptidase Y and leucine aminopeptidase. By following the polypeptide molecular species rather than the released residues, sequence information is obtained regardless of the relative rates of cleavage of peptide bonds. In addition, unambiguous assignments of sequence can be made in the presence of multiple identical residues. The lower level of sensitivity for the analysis is in the picomole range. When carboxypeptidase Y is used, the method provides a specific and sensitive method for the sequencing of polypeptides from the C-terminus.

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Year:  1986        PMID: 2425658     DOI: 10.1016/0003-2697(86)90035-7

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  6 in total

1.  Peptide sequence information derived by pronase digestion and ammonium sulfate in-source decay matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

Authors:  L A Marzilli; T R Golden; R J Cotter; A S Woods
Journal:  J Am Soc Mass Spectrom       Date:  2000-11       Impact factor: 3.109

2.  Matrix-assisted laser desorption/ionization mass spectrometry methods for oligodeoxynucleotides: improvements in matrix, detection limits, quantification, and sequencing.

Authors:  L K Zhang; M L Gross
Journal:  J Am Soc Mass Spectrom       Date:  2000-10       Impact factor: 3.109

3.  Identification of the posttranslational modifications of bovine lens alpha B-crystallins by mass spectrometry.

Authors:  J B Smith; Y Sun; D L Smith; B Green
Journal:  Protein Sci       Date:  1992-05       Impact factor: 6.725

4.  Determination of amide hydrogen exchange by mass spectrometry: a new tool for protein structure elucidation.

Authors:  Z Zhang; D L Smith
Journal:  Protein Sci       Date:  1993-04       Impact factor: 6.725

5.  Ammonium sulfate and MALDI in-source decay: a winning combination for sequencing peptides.

Authors:  Alice Delvolve; Amina S Woods
Journal:  Anal Chem       Date:  2009-12-01       Impact factor: 6.986

6.  Optimizing the MALDI-TOF-MS observation of peptides containing disulfide bonds.

Authors:  Kristin G Huwiler; Deane F Mosher; Martha M Vestling
Journal:  J Biomol Tech       Date:  2003-12
  6 in total

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