| Literature DB >> 26151661 |
John D Venable1, Caitlin Steckler1,2, Weijia Ou1, Jan Grünewald1, Sanjay Agarwalla1, Ansgar Brock1.
Abstract
Protein interaction surface mapping using MS is widely applied but comparatively resource-intensive. Here, a workflow adaptation for use of isotope-coded tandem mass tags for the purpose is reported. The key benefit of improved throughput derived from sample acquisition multiplexing and automated analysis is shown to be maintained in the new application. Mapping of the epitopes of two monoclonal antibodies on their respective targets serves to illustrate the novel approach. We conclude that the approach enables mapping of interactions by MS at significantly larger scales than hereto possible.Entities:
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Year: 2015 PMID: 26151661 PMCID: PMC4535432 DOI: 10.1021/acs.analchem.5b01410
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986