Protein modification by thiolactone homocysteine chemistry: A multifunctionalized human serum albumin theranostic

Tatyana V. Popova, Olesya A. Krumkacheva, Anna S. Burmakova, Anna S. Spitsyna, Olga D. Zakharova, Vladimir A. Lisitskiy, Igor A. Kirilyuk, Vladimir N. Silnikov, Michael K. Bowman, Elena G. Bagryanskaya, Tatyana S. Godovikova

Research output: Contribution to journalArticlepeer-review

Abstract

As the most abundant protein with a variety of physiological functions, albumin has been used extensively for the delivery of therapeutic molecules. Thiolactone chemistry provides a powerful tool to prepare spin-labeled albumin-based multimodal imaging probes and therapeutic agents. We report the synthesis of a tamoxifen homocysteine thiolactone derivative and its use in thiol-'click' chemistry to prepare multi-functionalized serum albumin. The released sulfhydryl group of the homocysteine functional handle was labeled with a nitroxide reagent to prepare a spin-labeled albumin-tamoxifen conjugate confirmed by MALDI-TOF-MS, EPR spectroscopy, UV-vis and fluorescent emission spectra. This is the basis for a novel multimodal tamoxifen-albumin theranostic with a significant (dose-dependent) inhibitory effect on the proliferation of malignant cells. The response of human glioblastoma multiforme T98G cells and breast cancer MCF-7 cells to tamoxifen and its albumin conjugates was different in tumor cells with different expression level of ERα in our experiments. These results provide further impetus to develop a serum protein for delivery of tamoxifen to cancer cells.

Original languageEnglish
Pages (from-to)1314-1325
Number of pages12
JournalRSC Medicinal Chemistry
Volume11
Issue number11
DOIs
Publication statusPublished - Nov 2020

Keywords

  • IN-VIVO
  • FC-RECEPTOR
  • SPIN-LABEL
  • HALF-LIFE
  • CONFORMATIONAL-CHANGES
  • FUNCTIONAL IMPAIRMENT
  • VERSATILE PLATFORM
  • CLICK CHEMISTRY
  • DRUG-DELIVERY
  • TAMOXIFEN

OECD FOS+WOS

  • 3.01 BASIC MEDICAL RESEARCH
  • 1.06 BIOLOGICAL SCIENCES

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