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Revealing the human mucinome. | LitMetric

Revealing the human mucinome.

Nat Commun

Department of Chemistry and Stanford ChEM-H, Stanford University, Stanford, 94305, CA, USA.

Published: June 2022

AI Article Synopsis

  • * Researchers studied a modified bacterial enzyme, StcE, which helps in isolating mucin-domain glycoproteins from complicated samples, enhancing our ability to identify them effectively.
  • * The developed mucinomics platform can uncover valuable molecular signatures related to cancer, using samples from both lab settings and real patients.

Article Abstract

Mucin domains are densely O-glycosylated modular protein domains found in various extracellular and transmembrane proteins. Mucin-domain glycoproteins play important roles in many human diseases, such as cancer and cystic fibrosis, but the scope of the mucinome remains poorly defined. Recently, we characterized a bacterial O-glycoprotease, StcE, and demonstrated that an inactive point mutant retains binding selectivity for mucin-domain glycoproteins. In this work, we leverage inactive StcE to selectively enrich and identify mucin-domain glycoproteins from complex samples like cell lysate and crude ovarian cancer patient ascites fluid. Our enrichment strategy is further aided by an algorithm to assign confidence to mucin-domain glycoprotein identifications. This mucinomics platform facilitates detection of hundreds of glycopeptides from mucin domains and highly overlapping populations of mucin-domain glycoproteins from ovarian cancer patients. Ultimately, we demonstrate our mucinomics approach can reveal key molecular signatures of cancer from in vitro and ex vivo sources.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9209528PMC
http://dx.doi.org/10.1038/s41467-022-31062-4DOI Listing

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