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000875158 1001_ $$00000-0001-6941-4808$$aKwon, Hanna$$b0
000875158 245__ $$aVisualizing the protons in a metalloenzyme electron proton transfer pathway
000875158 260__ $$aWashington, DC$$bNational Acad. of Sciences$$c2020
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000875158 520__ $$aIn redox metalloenzymes, the process of electron transfer often involves the concerted movement of a proton. These processes are referred to as proton-coupled electron transfer, and they underpin a wide variety of biological processes, including respiration, energy conversion, photosynthesis, and metalloenzyme catalysis. The mechanisms of proton delivery are incompletely understood, in part due to an absence of information on exact proton locations and hydrogen bonding structures in a bona fide metalloenzyme proton pathway. Here, we present a 2.1-Å neutron crystal structure of the complex formed between a redox metalloenzyme (ascorbate peroxidase) and its reducing substrate (ascorbate). In the neutron structure of the complex, the protonation states of the electron/proton donor (ascorbate) and all of the residues involved in the electron/proton transfer pathway are directly observed. This information sheds light on possible proton movements during heme-catalyzed oxygen activation, as well as on ascorbate oxidation.
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000875158 7001_ $$0P:(DE-HGF)0$$aBasran, Jaswir$$b1
000875158 7001_ $$00000-0001-5989-6794$$aDevos, Juliette M.$$b2
000875158 7001_ $$0P:(DE-HGF)0$$aSuardíaz, Reynier$$b3
000875158 7001_ $$0P:(DE-HGF)0$$avan der Kamp, Marc W.$$b4
000875158 7001_ $$0P:(DE-HGF)0$$aMulholland, Adrian J.$$b5
000875158 7001_ $$0P:(DE-Juel1)138266$$aSchrader, Tobias E.$$b6$$ufzj
000875158 7001_ $$0P:(DE-HGF)0$$aOstermann, Andreas$$b7
000875158 7001_ $$00000-0002-6412-4358$$aBlakeley, Matthew P.$$b8
000875158 7001_ $$00000-0003-1762-9238$$aMoody, Peter C. E.$$b9
000875158 7001_ $$00000-0002-1643-8694$$aRaven, Emma L.$$b10$$eCorresponding author
000875158 773__ $$0PERI:(DE-600)1461794-8$$a10.1073/pnas.1918936117$$gVol. 117, no. 12, p. 6484 - 6490$$n12$$p6484 - 6490$$tProceedings of the National Academy of Sciences of the United States of America$$v117$$x1091-6490$$y2020
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