Literature DB >> 18429134

Enzymatic approaches for obtaining amino acid sequence: on-target ladder sequencing.

C R Jiménez1, L Huang, Y Qiu, A L Burlingame.   

Abstract

Peptide sequencing by mass spectrometry (MS) is usually based on detecting mass differences associated with various amino acids in the polymer chain. Post-source decay (PSD) and MS/MS spectra may yield internal peptide sequences. However, determination of the order of the first two, and sometimes the last few, amino acids in the peptide is often problematic without additional experiments. Several enzymatic approaches have proven useful for identifying the N- and C-terminal residues. They involve the use of carboxypeptidases and aminopeptidases to produce peptide ladders for rapid analysis by matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS). This unit describes the ladder sequence method to generate amino acid sequence information from low- to subpicomole quantities of peptides. It can be performed directly on the sample stage, thus minimizing potential sample losses to vials and through sample transfer.

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Year:  2001        PMID: 18429134     DOI: 10.1002/0471140864.ps1607s15

Source DB:  PubMed          Journal:  Curr Protoc Protein Sci        ISSN: 1934-3655


  1 in total

1.  N-terminal protein characterization by mass spectrometry after cyanogen bromide cleavage using combined microscale liquid- and solid-phase derivatization.

Authors:  Heinz Nika; David H Hawke; Ruth Hogue Angeletti
Journal:  J Biomol Tech       Date:  2014-04
  1 in total

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