<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Anderson LC</submitter><funding>NIAID NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>617-624</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4379715</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>377</volume><pubmed_abstract>Previously, we described implementation of a front-end ETD (electron transfer dissociation) source for an Orbitrap instrument (1). This source facilitates multiple fills of the C-trap with product ions from ETD of intact proteins prior to mass analysis. The result is a dramatic enhancement of the observed ion current without the need for time consuming averaging of data from multiple mass measurements. Here we show that ion-ion proton transfer (IIPT) reactions can be used to simplify ETD spectra and to disperse fragment ions over the entire mass range in a controlled manner. We also show that protein derivatization can be employed to selectively enhance the sequence information observed at the N- and C-termini of a protein.</pubmed_abstract><journal>International journal of mass spectrometry</journal><pubmed_title>Protein derivatization and sequential ion/ion reactions to enhance sequence coverage produced by electron transfer dissociation mass spectrometry.</pubmed_title><pmcid>PMC4379715</pmcid><funding_grant_id>R01 GM037537</funding_grant_id><funding_grant_id>R37 AI033993</funding_grant_id><funding_grant_id>R01 AI033993</funding_grant_id><pubmed_authors>English AM</pubmed_authors><pubmed_authors>Shabanowitz J</pubmed_authors><pubmed_authors>Hunt DF</pubmed_authors><pubmed_authors>Bai DL</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Anderson LC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Protein derivatization and sequential ion/ion reactions to enhance sequence coverage produced by electron transfer dissociation mass spectrometry.</name><description>Previously, we described implementation of a front-end ETD (electron transfer dissociation) source for an Orbitrap instrument (1). This source facilitates multiple fills of the C-trap with product ions from ETD of intact proteins prior to mass analysis. The result is a dramatic enhancement of the observed ion current without the need for time consuming averaging of data from multiple mass measurements. Here we show that ion-ion proton transfer (IIPT) reactions can be used to simplify ETD spectra and to disperse fragment ions over the entire mass range in a controlled manner. We also show that protein derivatization can be employed to selectively enhance the sequence information observed at the N- and C-termini of a protein.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Feb</publication><modification>2020-10-29T11:47:15Z</modification><creation>2019-03-27T01:49:04Z</creation></dates><accession>S-EPMC4379715</accession><cross_references><pubmed>25844056</pubmed><doi>10.1016/j.ijms.2014.06.023</doi></cross_references></HashMap>