<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sherwood CA</submitter><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>3746-51</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2811718</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(7)</volume><pubmed_abstract>Multiple reaction monitoring (MRM) is a highly sensitive method of targeted mass spectrometry (MS) that can be used to selectively detect and quantify peptides based on the screening of specified precursor peptide-to-fragment ion transitions. MRM-MS sensitivity depends critically on the tuning of instrument parameters, such as collision energy and cone voltage, for the generation of maximal product ion signal. Although generalized equations and values exist for such instrument parameters, there is no clear indication that optimal signal can be reliably produced for all types of MRM transitions using such an algorithmic approach. To address this issue, we have devised a workflow functional on both Waters Quattro Premier and ABI 4000 QTRAP triple quadrupole instruments that allows rapid dete</pubmed_abstract><journal>Journal of proteome research</journal><pubmed_title>Rapid optimization of MRM-MS instrument parameters by subtle alteration of precursor and product m/z targets.</pubmed_title><pmcid>PMC2811718</pmcid><funding_grant_id>R21 CA126216-02</funding_grant_id><funding_grant_id>N01-HV-28179</funding_grant_id><funding_grant_id>R21 CA126216</funding_grant_id><funding_grant_id>P50GM076547</funding_grant_id><funding_grant_id>P50 GM076547</funding_grant_id><funding_grant_id>5R21CA126216</funding_grant_id><funding_grant_id>N01HV28179</funding_grant_id><funding_grant_id>P50 GM076547-03</funding_grant_id><pubmed_authors>Eastham A</pubmed_authors><pubmed_authors>Lee LW</pubmed_authors><pubmed_authors>Falkner JA</pubmed_authors><pubmed_authors>Sherwood CA</pubmed_authors><pubmed_authors>Mirzaei H</pubmed_authors><pubmed_authors>Martin DB</pubmed_authors><pubmed_authors>Risler J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rapid optimization of MRM-MS instrument parameters by subtle alteration of precursor and product m/z targets.</name><description>Multiple reaction monitoring (MRM) is a highly sensitive method of targeted mass spectrometry (MS) that can be used to selectively detect and quantify peptides based on the screening of specified precursor peptide-to-fragment ion transitions. MRM-MS sensitivity depends critically on the tuning of instrument parameters, such as collision energy and cone voltage, for the generation of maximal product ion signal. Although generalized equations and values exist for such instrument parameters, there is no clear indication that optimal signal can be reliably produced for all types of MRM transitions using such an algorithmic approach. To address this issue, we have devised a workflow functional on both Waters Quattro Premier and ABI 4000 QTRAP triple quadrupole instruments that allows rapid dete</description><dates><release>2009-01-01T00:00:00Z</release><publication>2009 Jul</publication><modification>2025-04-05T11:31:45.301Z</modification><creation>2019-03-27T00:28:09Z</creation></dates><accession>S-EPMC2811718</accession><cross_references><pubmed>19405522</pubmed><doi>10.1021/pr801122b</doi></cross_references></HashMap>