Literature DB >> 19338048

To b or not to b: the ongoing saga of peptide b ions.

Alex G Harrison1.   

Abstract

Modern soft ionization techniques readily produce protonated or multiply protonated peptides. Collision-induced dissociation (CID) of these protonated species is often used as a method to obtain sequence information. In many cases fragmentation occurs at amide bonds. When the charge resides on the C-terminal fragment so-called y ions are produced which are known to be protonated amino acids or truncated peptides. When the charge resides on the N-terminal fragment so-called b ions are produced. Often the sequence of y and b ions are essential for peptide sequencing. The b ions have many possible structures, a knowledge of which is useful in this sequencing. The structures of b ions are reviewed in the following with particular emphasis on the variation of structure with the number of amino acid residues in the b ion and the effect of peptide side chain on b ion structure. The recent discovery of full cyclization of larger b ions results in challenges in peptide sequencing. This aspect is discussed in detail. Copyright 2009 Wiley Periodicals, Inc.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19338048     DOI: 10.1002/mas.20228

Source DB:  PubMed          Journal:  Mass Spectrom Rev        ISSN: 0277-7037            Impact factor:   10.946


  49 in total

1.  Tryptic y(++) fragment ion distributions are guided by Coulombic repulsion.

Authors:  Karl K Irikura; John K Merle; Yamil Simón-Manso
Journal:  J Am Soc Mass Spectrom       Date:  2011-12-20       Impact factor: 3.109

2.  Rearrangement pathways of the a (4) ion of protonated YGGFL characterized by IR spectroscopy and modeling.

Authors:  Béla Paizs; Benjamin J Bythell; Philippe Maître
Journal:  J Am Soc Mass Spectrom       Date:  2012-01-24       Impact factor: 3.109

3.  Conformation-specific spectroscopy of peptide fragment ions in a low-temperature ion trap.

Authors:  Tobias N Wassermann; Oleg V Boyarkin; Béla Paizs; Thomas R Rizzo
Journal:  J Am Soc Mass Spectrom       Date:  2012-03-30       Impact factor: 3.109

4.  Mass spectrometry analysis of 2-nitrophenylhydrazine carboxy derivatized peptides.

Authors:  Junmei Zhang; Rowaida Al-Eryani; Haydn L Ball
Journal:  J Am Soc Mass Spectrom       Date:  2011-08-04       Impact factor: 3.109

5.  Sequence scrambling in shotgun proteomics is negligible.

Authors:  Anton A Goloborodko; Mikhail V Gorshkov; David M Good; Roman A Zubarev
Journal:  J Am Soc Mass Spectrom       Date:  2011-04-15       Impact factor: 3.109

6.  The relative charge ratio between C and N atoms in amide bond acts as a key factor to determine peptide fragment efficiency in different charge states.

Authors:  Feng Sun; Wansong Zong; Rutao Liu; Meijie Wang; Pengjun Zhang; Qifei Xu
Journal:  J Am Soc Mass Spectrom       Date:  2010-07-08       Impact factor: 3.109

7.  Effect of the His residue on the cyclization of b ions.

Authors:  Benjamin J Bythell; Michaela Knapp-Mohammady; Béla Paizs; Alex G Harrison
Journal:  J Am Soc Mass Spectrom       Date:  2010-05-13       Impact factor: 3.109

8.  The extent and effects of peptide sequence scrambling via formation of macrocyclic B ions in model proteins.

Authors:  Irine S Saminathan; X Simon Wang; Yuzhu Guo; Olga Krakovska; Sébastien Voisin; Alan C Hopkinson; K W Michael Siu
Journal:  J Am Soc Mass Spectrom       Date:  2010-09-09       Impact factor: 3.109

9.  Fragmentation reactions of b(5) and a (5) ions containing proline--the structures of a(5) ions.

Authors:  Alex G Harrison
Journal:  J Am Soc Mass Spectrom       Date:  2011-09-20       Impact factor: 3.109

10.  Influence of a Gamma Amino Acid on the Structures and Reactivity of Peptide a(3) Ions.

Authors:  Matthew C Bernier; Bela Paizs; Vicki H Wysocki
Journal:  Int J Mass Spectrom       Date:  2012-04-15       Impact factor: 1.986

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.