<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bache N</submitter><funding>EC | Horizon 2020 Framework Programme</funding><funding>Novo Nordisk Foundation Center for Protein Research</funding><funding>Novo Nordisk Fonden</funding><funding>Max-Planck-Gesellschaft</funding><pagination>2284-2296</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6210218</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(11)</volume><pubmed_abstract>To further integrate mass spectrometry (MS)-based proteomics into biomedical research and especially into clinical settings, high throughput and robustness are essential requirements. They are largely met in high-flow rate chromatographic systems for small molecules but these are not sufficiently sensitive for proteomics applications. Here we describe a new concept that delivers on these requirements while maintaining the sensitivity of current nano-flow LC systems. Low-pressure pumps elute the sample from a disposable trap column, simultaneously forming a chromatographic gradient that is stored in a long storage loop. An auxiliary gradient creates an offset, ensuring the re-focusing of the peptides before the separation on the analytical column by a single high-pressure pump. This simplif</pubmed_abstract><journal>Molecular &amp; cellular proteomics : MCP</journal><pubmed_title>A Novel LC System Embeds Analytes in Pre-formed Gradients for Rapid, Ultra-robust Proteomics.</pubmed_title><pmcid>PMC6210218</pmcid><funding_grant_id>NNF15SA0018240</funding_grant_id><funding_grant_id>MPI</funding_grant_id><funding_grant_id>grant NNF14CC0001</funding_grant_id><funding_grant_id>PI Matthias Mann</funding_grant_id><funding_grant_id>grant agreement no 686547 MSmed project</funding_grant_id><funding_grant_id>PI Jesper Velgaard Olsen</funding_grant_id><pubmed_authors>Doll S</pubmed_authors><pubmed_authors>Bache N</pubmed_authors><pubmed_authors>Geyer PE</pubmed_authors><pubmed_authors>Treit PV</pubmed_authors><pubmed_authors>Muller JB</pubmed_authors><pubmed_authors>Mann M</pubmed_authors><pubmed_authors>Olsen JV</pubmed_authors><pubmed_authors>Vorm O</pubmed_authors><pubmed_authors>Falkenby L</pubmed_authors><pubmed_authors>Meier F</pubmed_authors><pubmed_authors>Hoerning O</pubmed_authors><pubmed_authors>Paron I</pubmed_authors><pubmed_authors>Bekker-Jensen DB</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Novel LC System Embeds Analytes in Pre-formed Gradients for Rapid, Ultra-robust Proteomics.</name><description>To further integrate mass spectrometry (MS)-based proteomics into biomedical research and especially into clinical settings, high throughput and robustness are essential requirements. They are largely met in high-flow rate chromatographic systems for small molecules but these are not sufficiently sensitive for proteomics applications. Here we describe a new concept that delivers on these requirements while maintaining the sensitivity of current nano-flow LC systems. Low-pressure pumps elute the sample from a disposable trap column, simultaneously forming a chromatographic gradient that is stored in a long storage loop. An auxiliary gradient creates an offset, ensuring the re-focusing of the peptides before the separation on the analytical column by a single high-pressure pump. This simplif</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Nov</publication><modification>2026-05-01T15:27:12.963Z</modification><creation>2019-03-26T22:50:19Z</creation></dates><accession>S-EPMC6210218</accession><cross_references><pubmed>30104208</pubmed><doi>10.1074/mcp.TIR118.000853</doi></cross_references></HashMap>