Literature DB >> 16401509

Collision-induced dissociation (CID) of peptides and proteins.

J Mitchell Wells1, Scott A McLuckey.   

Abstract

The most commonly used activation method in the tandem mass spectrometry (MS) of peptides and proteins is energetic collisions with a neutral target gas. The overall process of collisional activation followed by fragmentation of the ion is commonly referred to as collision-induced dissociation (CID). The structural information that results from CID of a peptide or protein ion is highly dependent on the conditions used to effect CID. These include, for example, the relative translational energy of the ion and target, the nature of the target, the number of collisions that is likely to take place, and the observation window of the apparatus. This chapter summarizes the key experimental parameters in the CID of peptide and protein ions, as well as the conditions that tend to prevail in the most commonly employed tandem mass spectrometers.

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Year:  2005        PMID: 16401509     DOI: 10.1016/S0076-6879(05)02005-7

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  120 in total

1.  Carbonyl charge solvation patterns may relate to fragmentation classes in collision-activated dissociation.

Authors:  Hongqian Yang; David M Good; David van der Spoel; Roman A Zubarev
Journal:  J Am Soc Mass Spectrom       Date:  2012-06-12       Impact factor: 3.109

Review 2.  Chemical and biochemical approaches in the study of histone methylation and demethylation.

Authors:  Keqin Kathy Li; Cheng Luo; Dongxia Wang; Hualiang Jiang; Y George Zheng
Journal:  Med Res Rev       Date:  2012-07       Impact factor: 12.944

3.  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

4.  Adaptation of a 3-D quadrupole ion trap for dipolar DC collisional activation.

Authors:  Boone M Prentice; Robert E Santini; Scott A McLuckey
Journal:  J Am Soc Mass Spectrom       Date:  2011-06-23       Impact factor: 3.109

5.  Dipolar DC collisional activation in a “stretched” 3-D ion trap: the effect of higher order fields on rf-heating.

Authors:  Boone M Prentice; Scott A McLuckey
Journal:  J Am Soc Mass Spectrom       Date:  2012-04       Impact factor: 3.109

6.  Theoretical Study of Dual-Direction Dipolar Excitation of Ions in Linear Ion Traps.

Authors:  Qiankun Dang; Fuxing Xu; Liang Wang; Xiaohua Huang; Xinhua Dai; Xiang Fang; Rizhi Wang; Chuan-Fan Ding
Journal:  J Am Soc Mass Spectrom       Date:  2016-01-26       Impact factor: 3.109

7.  Ion trap collisional activation of c and z* ions formed via gas-phase ion/ion electron-transfer dissociation.

Authors:  Hongling Han; Yu Xia; Scott A McLuckey
Journal:  J Proteome Res       Date:  2007-07-03       Impact factor: 4.466

Review 8.  Methods and approaches for the comprehensive characterization and quantification of cellular proteomes using mass spectrometry.

Authors:  Shama P Mirza; Michael Olivier
Journal:  Physiol Genomics       Date:  2007-12-27       Impact factor: 3.107

9.  Fragmentation of phosphorylated and singly charged peptide ions via interaction with metastable atoms.

Authors:  Vadym D Berkout; Vladimir M Doroshenko
Journal:  Int J Mass Spectrom       Date:  2008-12-01       Impact factor: 1.986

10.  Multiple Reaction Monitoring for Direct Quantitation of Intact Proteins Using a Triple Quadrupole Mass Spectrometer.

Authors:  Evelyn H Wang; Peter C Combe; Kevin A Schug
Journal:  J Am Soc Mass Spectrom       Date:  2016-03-08       Impact factor: 3.109

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