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Disorder in protein structures is critical to their biological functions but can also contribute to diseases. Our work introduces a new way to characterize protein disorder in biological systems, complementing existing '-omics' approaches and computational prediction methods.
Researchers present a proteome-wide workflow using the bifunctional chemical probe TME to capture, enrich, and profile endogenous disordered proteins in cells.View quoted post on X
@shouxiang_zhang @owyongtc @yuning_hong @LIMSLTU @latrobe
nature.com/articles/s4159…