Chemical Generation of Hydroxyl Radical for Oxidative 'Footprinting'

被引:14
|
作者
Leser, Micheal [1 ]
Chapman, Jessica R. [2 ]
Khine, Michelle [3 ,4 ]
Pegan, Jonathan [3 ]
Law, Matt [4 ,5 ]
El Makkaoui, Mohammed [4 ,5 ]
Ueberheide, Beatrix M. [2 ,6 ]
Brenowitz, Michael [1 ]
机构
[1] Albert Einstein Coll Med, Dept Biochem, Bronx, NY 10467 USA
[2] NYU, Sch Med, Dept Biochem, Prote Lab, New York, NY 10016 USA
[3] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA USA
[4] Univ Calif Irvine, Dept Chem Engn & Mat Sci, Irvine, CA USA
[5] Univ Calif Irvine, Dept Chem, Irvine, CA 92717 USA
[6] NYU, Dept Biochem & Mol Pharmacol, Sch Med, New York, NY 10003 USA
来源
PROTEIN AND PEPTIDE LETTERS | 2019年 / 26卷 / 01期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Fenton reaction; footprinting; hydroxyl radical; protein; structure mapping; mass spectrometry; AMINO-ACID-RESIDUES; ACCESSIBLE SURFACE-AREAS; RADIOLYTIC MODIFICATION; FOLDING PATHWAY; NUCLEIC-ACIDS; PROTEIN; RNA; DNA; PEPTIDES; OXYGEN;
D O I
10.2174/0929866526666181212164812
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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-S-2, 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-L I. 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.
引用
收藏
页码:61 / 69
页数:9
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