| Literature DB >> 28146308 |
James Murray1, Jaehwan Sim2, Kyunghoon Oh3, Gihyun Sung3, Ara Lee3, Annadka Shrinidhi1, Ayyavu Thirunarayanan1, Dinesh Shetty1, Kimoon Kim1,2,4,3.
Abstract
Chemical proteomics relies primarily on click-chemistry-based protein labeling and biotin-streptavidin enrichment, but these techniques have inherent limitations. Enrichment of intracellular proteins using a totally synthetic host-guest complex is described, overcoming the problem associated with the classical approach. We achieve this by affinity-based protein labeling with a target-specific probe molecule conjugated to a high-affinity guest (suberanilohydroxamic acid-ammonium-adamantane; SAHA-Ad) and then enriching the labeled species using a cucurbit[7]uril bead. This method shows high specificity for labeled molecules in a MDA-MB-231 breast cancer cell lysate. Moreover, this method shows promise for labeling proteins in live cells.Entities:
Keywords: cucurbiturils; host-guest chemistry; protein chemistry; protein enrichment; supramolecular chemistry
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Year: 2017 PMID: 28146308 DOI: 10.1002/anie.201611894
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336