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.
Original language | British English |
---|---|
Pages (from-to) | 2395-2398 |
Number of pages | 4 |
Journal | Angewandte Chemie - International Edition |
Volume | 56 |
Issue number | 9 |
DOIs | |
State | Published - 20 Feb 2017 |
Keywords
- cucurbiturils
- host–guest chemistry
- protein chemistry
- protein enrichment
- supramolecular chemistry