<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Des Soye BJ</submitter><funding>Northwestern Memorial Foundation</funding><funding>Walder Foundation</funding><funding>Northwestern University Clinical and Translational Sciences Institute</funding><funding>NIH Office of the Director</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>National Institute of General Medical Sciences</funding><funding>NIH HHS</funding><funding>NIGMS NIH HHS</funding><pubmed_abstract>Charge detection mass spectrometry (CDMS) is a well-established technique that provides direct mass spectral outputs regardless of analyte heterogeneity or molecular weight. Over the past few years, it has been demonstrated that CDMS can be multiplexed on Orbitrap analyzers utilizing an integrated approach termed individual ion mass spectrometry (I&lt;sup>2&lt;/sup>MS). To further increase adaptability, robustness, and throughput of this technique, here, we present a method that utilizes numerous integrated equipment components including a Kingfisher system, SampleStream platform, and Q Exactive mass spectrometer to provide a fully automated workflow for immunoprecipitation, sample preparation, injection, and subsequent I&lt;sup>2&lt;/sup>MS acquisition. This automated workflow has been applied to a c</pubmed_abstract><journal>Analytical chemistry</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11825902</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Automated Immunoprecipitation, Sample Preparation, and Individual Ion Mass Spectrometry Platform for Proteoforms.</pubmed_title><pmcid>PMC11825902</pmcid><funding_grant_id>S10 OD025194</funding_grant_id><funding_grant_id>P30 CA060553</funding_grant_id><funding_grant_id>NCI CCSG P30 CA060553</funding_grant_id><funding_grant_id>P41 GM108569</funding_grant_id><funding_grant_id>SCI16</funding_grant_id><pubmed_authors>Des Soye BJ</pubmed_authors><pubmed_authors>Fellers RT</pubmed_authors><pubmed_authors>Forte E</pubmed_authors><pubmed_authors>Hollas MAR</pubmed_authors><pubmed_authors>Melani RD</pubmed_authors><pubmed_authors>Kafader JO</pubmed_authors><pubmed_authors>McGee JP</pubmed_authors><pubmed_authors>Kelleher NL</pubmed_authors><pubmed_authors>Wilkins JT</pubmed_authors><pubmed_authors>Compton PD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Automated Immunoprecipitation, Sample Preparation, and Individual Ion Mass Spectrometry Platform for Proteoforms.</name><description>Charge detection mass spectrometry (CDMS) is a well-established technique that provides direct mass spectral outputs regardless of analyte heterogeneity or molecular weight. Over the past few years, it has been demonstrated that CDMS can be multiplexed on Orbitrap analyzers utilizing an integrated approach termed individual ion mass spectrometry (I&lt;sup>2&lt;/sup>MS). To further increase adaptability, robustness, and throughput of this technique, here, we present a method that utilizes numerous integrated equipment components including a Kingfisher system, SampleStream platform, and Q Exactive mass spectrometer to provide a fully automated workflow for immunoprecipitation, sample preparation, injection, and subsequent I&lt;sup>2&lt;/sup>MS acquisition. This automated workflow has been applied to a c</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-07-15T18:06:49.912Z</modification><creation>2026-07-08T03:08:43.272Z</creation></dates><accession>S-EPMC11825902</accession><cross_references><pubmed>39143757</pubmed><doi>10.1021/acs.analchem.4c01962</doi></cross_references></HashMap>