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N Engl J Med 316:971977

In the present study, we pursued a chemoproteomic approach that leverages broadly interactive, fragment-based photoaffinity probes to map reversible small-moleculeprotein interactions as a function of phosphorylation and glycosylation status directly in cells (Fig

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( B ) Increase of pS6 (gMFI was normalized to that in unstimulated blood) in pDCs and cDCs with different severity grades determined during an OFC and ( C ) categorized into low (grade 2) versus high (grade 3 and 4 together) groups ( n = 61)