4.5 Article

Proof of concept: Pull down assay using bovine serum albumin and an immunomodulator small molecule

Journal

HELIYON
Volume 9, Issue 11, Pages -

Publisher

CELL PRESS
DOI: 10.1016/j.heliyon.2023.e21408

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This study presents a method for identifying the cellular targets of Compound A in human peripheral blood mononuclear cells (PBMCs). By synthesizing a probe based on the chemical structure of Compound A and demonstrating its efficient binding to bovine serum albumin, this method can be used to further identify potential protein targets of small molecules in living cells. These findings provide a valuable starting point for exploring the molecular mechanisms underlying the immunomodulatory effects of Compound A.
In the past decade, there has been increasing interest in use of small molecules for immunomodulation. The affinity-based pull-down purification is an essential tool for target identification of small molecules and drug discovery. This study presents our recent efforts to investigate the cellular target(s) of Compound A, a small molecule with demonstrated immunomodulatory properties in human peripheral blood mononuclear cells (PBMCs). While we have previously observed the immunomodulatory activity of Compound A in PBMCs, the specific molecular targets underlying its effects remains elusive. To address this challenge, we synthesized a trifluoromethyl phenyl diazirine (TPD)-bearing trifunctional Probe 1 based on the chemical structure of Compound A, which could be used in a pull-down assay to efficiently bind to putative cellular targets via photoaffinity labelling. In this report, we utilized bovine serum albumin (BSA) as a model protein to establish a proof-of-concept in order to assess the suitability of Probe 1 for binding to an endogenous target. By the successful synthesis of Probe 1 and demonstrating the efficient binding of Probe 1 to BSA, we propose that this method can be used as a tool for further identification of potential protein targets of small molecules in living cells. Our findings provide a valuable starting point for further investigations into the molecular mechanisms underlying the immunomodulatory effects of Compound A.

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