Literature DB >> 12768604

Reactions of polypeptide ions with electrons in the gas phase.

Roman A Zubarev1.   

Abstract

Reactions of electrons in the energy range below 70 eV with polypeptide cations and anions are reviewed, as well as their applications for the structural analysis of polypeptides. At very low energies (</= 0.1 eV), the major outcome is electron-capture dissociation (ECD) of S-S and backbone N-C(alpha) bonds, leading to c' and z. fragments. ECD is useful in sequencing and characterization of post-translational modifications (PTMs), because c', z. fragmentation is abundant and the fragments usually retain labile groups. Electron capture at higher energies (3-13 eV) induces secondary fragmentation in radical z. fragments; this hot ECD (HECD) allows one to distinguish between the isomeric leucine and isoleucine residues. If a hot electron is not captured, then the induced electronic excitation converts internally into vibrational energy, resulting in fragmentation of the C(O)bond;N backbone bond (so-called EIEIO process). Above 9-10 eV, further ionization of n-charged cations occurs. If the formed (n + 1)+. cations capture electrons, then the C(alpha)bond;C backbone bond is usually broken. For anions that collide with approximately 20 eV electrons, the ejection of an electron leads to the creation of a radical positive charge (hole) that recombines internally with a negative charge. Such recombination leads to various backbone bond cleavages. This electron-detachment dissociation (EDD) is analogous to ECD for negative ions. Copyright 2003 Wiley Periodicals, Inc., Mass Spec Rev 22:57-77, 2003; Published online in Wiley InterScience (www.interscience.wiley.com)

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Year:  2003        PMID: 12768604     DOI: 10.1002/mas.10042

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


  119 in total

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2.  Peptide and protein sequence analysis by electron transfer dissociation mass spectrometry.

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Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-21       Impact factor: 11.205

3.  Effects of charge state and cationizing agent on the electron capture dissociation of a peptide.

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Journal:  Anal Chem       Date:  2004-04-15       Impact factor: 6.986

4.  Defining intact protein primary structures from saliva: a step toward the human proteome project.

Authors:  F Halgand; V Zabrouskov; S Bassilian; P Souda; J A Loo; K F Faull; D T Wong; J P Whitelegge
Journal:  Anal Chem       Date:  2012-05-02       Impact factor: 6.986

5.  Sequence analysis of peptide:oligonucleotide heteroconjugates by electron capture dissociation and electron transfer dissociation.

Authors:  Kady L Krivos; Patrick A Limbach
Journal:  J Am Soc Mass Spectrom       Date:  2010-04-03       Impact factor: 3.109

6.  Tandem MS analysis of selenamide-derivatized peptide ions.

Authors:  Yun Zhang; Hao Zhang; Weidong Cui; Hao Chen
Journal:  J Am Soc Mass Spectrom       Date:  2011-06-09       Impact factor: 3.109

7.  Electron transfer dissociation of doubly sodiated glycerophosphocholine lipids.

Authors:  Xiaorong Liang; Jian Liu; Yves LeBlanc; Tom Covey; A Celeste Ptak; J Thomas Brenna; Scott A McLuckey
Journal:  J Am Soc Mass Spectrom       Date:  2007-07-26       Impact factor: 3.109

8.  Electron-transfer reagent anion formation via electrospray ionization and collision-induced dissociation.

Authors:  Teng-Yi Huang; Joshua F Emory; Richard A J O'Hair; Scott A McLuckey
Journal:  Anal Chem       Date:  2006-11-01       Impact factor: 6.986

9.  Electron detachment dissociation of glycosaminoglycan tetrasaccharides.

Authors:  Jeremy J Wolff; I Jonathan Amster; Lianli Chi; Robert J Linhardt
Journal:  J Am Soc Mass Spectrom       Date:  2006-10-30       Impact factor: 3.109

Review 10.  On-line separations combined with MS for analysis of glycosaminoglycans.

Authors:  Joseph Zaia
Journal:  Mass Spectrom Rev       Date:  2009 Mar-Apr       Impact factor: 10.946

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