Interaction profiling methods to map protein and pathway targets of bioactive ligands.

Abstract:

:Recent advances in -omic profiling technologies have ushered in an era where we no longer want to merely measure the presence or absence of a biomolecule of interest, but instead hope to understand its function and interactions within larger signaling networks. Here, we review several emerging proteomic technologies capable of detecting protein interaction networks in live cells and their integration to draft holistic maps of proteins that respond to diverse stimuli, including bioactive small molecules. Moreover, we provide a conceptual framework to combine so-called 'top-down' and 'bottom-up' interaction profiling methods and ensuing proteomic profiles to directly identify binding targets of small molecule ligands, as well as for unbiased discovery of proteins and pathways that may be directly bound or influenced by those first responders. The integrated, interaction-based profiling methods discussed here have the potential to provide a unique and dynamic view into cellular signaling networks for both basic and translational biological studies.

journal_name

Curr Opin Chem Biol

authors

Huang JX,Coukos JS,Moellering RE

doi

10.1016/j.cbpa.2020.02.001

subject

Has Abstract

pub_date

2020-02-01 00:00:00

pages

76-84

eissn

1367-5931

issn

1879-0402

pii

S1367-5931(20)30017-X

journal_volume

54

pub_type

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