Phosphonic acid

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UNIPROT ID/AC

160488.PP_0985 (1)
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CHEBI:15347 (2)
CHEBI:37084 (2)
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CHEBI:15428 (2)
CHEBI:18123 (2)
CHEBI:27266 (2)
CHEBI:16449 (2)
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CHEBI:30769 (2)
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CHEBI:40750 (1)
CHEBI:39640|CHEBI:39866 (1)
CHEBI:27471|CHEBI:36274 (1)
CHEBI:134207 (1)
CHEBI:443725 (1)
CHEBI:84805 (1)
CHEBI:27859 (1)

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Lab affiliation

1. Laboratoire de Spectrométrie de Masse BioOrganique, IPHC UMR 7178, Université de Strasbourg, CNRS, 67000 Strasbourg, France 2. Infrastructure Nationale de Protéomique ProFI – FR2048, 67087 Strasbourg, France (1)
Biomolecular Mass Spectrometry Pharmaceutical Sciences Utrecht University (1)
Biomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Padualaan 8, 3584 CH Utrecht, The Netherlands (1)
Department of Cell Biology Harvard Medical School Boston, MA, USA (1)
Immunomodulation Group, Navarrabiomed Biomedical Research Center, Institute of Health Carlos III (ISCIII), Navarra Institute for Health Research (IdiSNA), Spain (1)
Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP) Robert-Rössle-Strasse 10, 13125 Berlin (Germany) Department of Chemistry, Humboldt Universität zu Berlin Brook-Taylor-Straße 2, 12489 Berlin (Germany) (1)

Tags

xref:PubMed:31585079 (1)

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Enriching cysteine-containing peptides using a sulfhydryl-reactive alkylating reagent with a phosphonic acid group, and immobilized metal affinity chromatography

The reduction of disulfide bonds and their subsequent alkylation is commonplace in typical proteomics workflows. Here, we highlight a sulfhydryl-reactive alkylating reagent with a phosphonic acid group (iodoacetamido-LC-phosphonic acid, 6C-CysPAT) that facilitates the enrichment of cysteine-containi...

ORGANISM(S): Homo sapiens (Human)

2023-12-28 | PXD038382 | Pride