Mapping Protein−Protein Interactions by Localized Oxidation: Consequences of the Reach of Hydroxyl Radical

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• 作者：Sarah M. Cheal ; Mindy Ng ; Brianda Barrios ; Zheng Miao ; Amir K. Kalani ; Claude F. Meares
• 刊名：Biochemistry
• 出版年：2009
• 出版时间：June 2, 2009
• 年：2009
• 卷：48
• 期：21
• 页码：4577-4586
• 全文大小：1086K
• 年卷期：v.48,no.21(June 2, 2009)
• ISSN：1520-4995

文摘

Hydroxyl radicals generated from a variety of methods, including not only synchrotron radiation but also Fenton reactions involving chelated iron, have become an accepted macromolecular footprinting tool. Hydroxyl radicals react with proteins via multiple mechanisms that lead to both polypeptide backbone cleavage events and side chain modifications (e.g., hydroxylation and carbonyl formation). The use of site-specifically tethered iron chelates can reveal protein−protein interactions, but the interpretation of such experiments will be strengthened by improving our understanding of how hydroxyl radicals produced at a point on a protein react with other protein sites. We have developed methods for monitoring carbonyl formation on proteins as a function of distance from a hydroxyl generator, iron-(S)-1-[p-(bromoacetamido)benzyl]EDTA (FeBABE), conjugated to an engineered cysteine residue. After activation of the chelated iron with ascorbate and peroxide produces new protein carbonyl groups, their positions can be identified using element-coded affinity tagging (ECAT), with carbonyl-specific tags {e.g., rare earth chelates of (S)-2-[4-(2-aminooxy)acetamidobenzyl]-1,4,7,10-tetraazacyclododecane-N,N′,N′′,N′′′-tetraacetic acid (AOD)} that allow for affinity purification, identification, and relative quantitation of oxidation sites using mass spectrometry. Intraprotein oxidation of single-cysteine mutants of Escherichia coli σ⁷⁰ by tethered FeBABE was used to calibrate the reach of hydroxyl radical by comparison to the crystal structure; the application to protein−protein interactions was demonstrated using the same σ⁷⁰ FeBABE conjugates in complexes with the RNA polymerase core enzyme. The results provide fundamental information for interpreting protein footprinting experiments in other systems.