Chemical Generation of Hydroxyl Radical for Oxidative ‘Footprinting’

Author:

Leser Micheal1,Chapman Jessica R.2,Khine Michelle3,Pegan Jonathan3,Law Matt4,Makkaoui Mohammed El4,Ueberheide Beatrix M.2,Brenowitz Michael1

Affiliation:

1. Department of Biochemistry, Albert Einstein College of Medicine, Bronx, NY, United States

2. Proteomics Laboratory, Department of Biochemistry, New York University School of Medicine, New York, NY, United States

3. Department of Biomedical Engineering, University of California, Irvine, CA, United States

4. Department of Chemical Engineering & Materials Science, University of California, Irvine, CA, United States

Abstract

Background: For almost four decades, hydroxyl radical chemically generated by Fenton chemistry has been a mainstay for the oxidative ‘footprinting’ of macromolecules. Objective: In this article, we start by reviewing the application of chemical generation of hydroxyl radical to the development of oxidative footprinting of DNA and RNA and the subsequent application of the method to oxidative footprinting of proteins. We next discuss a novel strategy for generating hydroxyl radicals by Fenton chemistry that immobilizes catalytic iron on a solid surface (Pyrite Shrink Wrap laminate) for the application of nucleic acid and protein footprinting. Method: Pyrite Shrink-Wrap Laminate is fabricated by depositing pyrite (Fe-S2, aka ‘fool’s gold’) nanocrystals onto thermolabile plastic (Shrinky Dink). The laminate can be thermoformed into a microtiter plate format into which samples are deposited for oxidation. Results: We demonstrate the utility of the Pyrite Shrink-Wrap Laminate for the chemical generation of hydroxyl radicals by mapping the surface of the T-cell co-stimulatory protein Programmed Death – 1 (PD-1) and the interface of the complex with its ligand PD-L1. Conclusion: We have developed and validated an affordable and reliable benchtop method of hydroxyl radical generation that will broaden the application of protein oxidative footprinting. Due to the minimal equipment required to implement this method, it should be easily adaptable by many laboratories with access to mass spectrometry.

Funder

National Institutes of Health

National Science Foundation

Publisher

Bentham Science Publishers Ltd.

Subject

Biochemistry,General Medicine,Structural Biology

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