Target Profiling of an Anticancer Drug Curcumin by an In Situ Chemical Proteomics Approach

Methods Mol Biol. 2021:2213:147-161. doi: 10.1007/978-1-0716-0954-5_13.

Abstract

Interdisciplinary chemical proteomics approaches have been widely applied to the identification of specific targets of bioactive small molecules or drugs. In this chapter, we describe the application of a cell-permeable activity-based curcumin probe (Cur-P) with an alkyne moiety to detect and identify specific binding targets of curcumin in HCT116 colon cancer cells. Through click chemistry, a fluorescent tag or a biotin tag is attached to the probe-modified curcumin targets for visualization or affinity purification followed by mass spectrometric identification. A quantitative proteomics approach of isobaric tags for relative and absolute quantification (iTRAQ)™ is applied to distinguish specific curcumin targets from nonspecific binding proteins.

Keywords: Activity-Based probe; Chemical proteomics; Curcumin; Mass spectrometry; Target identification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Chromatography, Ion Exchange
  • Chromatography, Liquid
  • Click Chemistry
  • Curcumin / pharmacology*
  • Electrophoresis, Polyacrylamide Gel
  • Fluorescence
  • HCT116 Cells
  • Humans
  • Isotope Labeling
  • Nanotechnology
  • Peptides / metabolism
  • Proteomics / methods*
  • Rhodamines
  • Streptavidin / chemistry
  • Tandem Mass Spectrometry
  • Trypsin / metabolism

Substances

  • Antineoplastic Agents
  • Peptides
  • Rhodamines
  • Streptavidin
  • Trypsin
  • Curcumin