Our program is devoted to answering key questions in biology through the development and application of multinuclear electron-nuclear double resonance (ENDOR) and electron spin-echo envelope modulation (ESEEM) spectroscopies to characterize transition-metal centers vital to human health and disease. Application of these techniques to intermediate states that are trapped by freeze-quench and cryoreduction methods, and are isotopically labeled by outstanding teams of collaborating chemists and biologists, can completely characterize the active-site environment of a metal ion at every stage of an enzyme's catalytic cycle. As augmented by novel kinetic protocols we have developed, these studies reveal in precise details the function of critical metal centers, not only in isolate enzymes but in living cells as well. Dramatic progress during our current grant period has inspired multiple specific aims: (i) Small-molecule activation by metalloenzymes, including Dioxygen-activation by Heme Monooxygenases and Dinitrogen Reduction by Nitrogenase; (ii) Biomimetic Mo and Fe Complexes as Models for Nitrogenase Intermediates and Paradigms for the Jahn-Taller Effect in trigonal symmetry; (iii) Radical Reactions in Metalloenzymes -The Radical SAM Superfamily; (iv) in vivo Speciation of Mn(II) - Protection from Oxidative Stress, Mechanisms of Toxicity, Probe of Physiology; (v) ATPase Co(II)/Mn(II) Transporters; (vi) ENDOR Methodology Development - Hyperfine Signs, Electron-Nuclear-Electron Triple Resonance, Q-band Resonator Development; (vii) Extending the Biological Applications of ENDOR Techniques. Many of these aims reflect longstanding efforts, while projects associated with transition-metal homeostasis that emerged this period (Mn(II) speciation, and Mn(II)/Co(II) transport) reflect a commitment to opening new areas, as explicitly expressed in the final Aim.

Public Health Relevance

Metal centers play a central role in human health and disease. Our program is devoted to the development and application of advanced paramagnetic resonance measurement techniques (ENDOR/ESEEM) as a uniquely incisive means of revealing how biologically important metal centers function. The systems to be studied play many essential roles, including: protection from oxidative stress and reactive-oxygen species (ROS); formation of the key signaling and immune-response molecules, nitric oxide and carbon monoxide; xenobiotic and drug metabolism; formation of essential cofactors, whose absence through genetic deficiencies is deadly; homeostasis of metal ions (Mn/Co/Fe) whose regulation in humans and pathogens is central in health and disease; enzymatic formation of the bio-available nitrogen on which two-thirds of the world's population depend.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM111097-45
Application #
9211337
Study Section
Special Emphasis Panel (ZRG1-BCMB-B (02)M)
Program Officer
Anderson, Vernon
Project Start
1979-01-01
Project End
2018-01-31
Budget Start
2017-02-01
Budget End
2018-01-31
Support Year
45
Fiscal Year
2017
Total Cost
$486,990
Indirect Cost
$171,786
Name
Northwestern University at Chicago
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
160079455
City
Evanston
State
IL
Country
United States
Zip Code
60201
Broderick, William E; Hoffman, Brian M; Broderick, Joan B (2018) Mechanism of Radical Initiation in the Radical S-Adenosyl-l-methionine Superfamily. Acc Chem Res 51:2611-2619
Fisher, Oriana S; Kenney, Grace E; Ross, Matthew O et al. (2018) Characterization of a long overlooked copper protein from methane- and ammonia-oxidizing bacteria. Nat Commun 9:4276
Gallagher, Audrey T; Lee, Jung Yoon; Kathiresan, Venkatesan et al. (2018) A structurally-characterized peroxomanganese(iv) porphyrin from reversible O2 binding within a metal-organic framework. Chem Sci 9:1596-1603
Raugei, Simone; Seefeldt, Lance C; Hoffman, Brian M (2018) Critical computational analysis illuminates the reductive-elimination mechanism that activates nitrogenase for N2 reduction. Proc Natl Acad Sci U S A 115:E10521-E10530
Byer, Amanda S; Yang, Hao; McDaniel, Elizabeth C et al. (2018) Paradigm Shift for Radical S-Adenosyl-l-methionine Reactions: The Organometallic Intermediate ? Is Central to Catalysis. J Am Chem Soc 140:8634-8638
Lukoyanov, Dmitriy A; Khadka, Nimesh; Yang, Zhi-Yong et al. (2018) Hydride Conformers of the Nitrogenase FeMo-cofactor Two-Electron Reduced State E2(2H), Assigned Using Cryogenic Intra Electron Paramagnetic Resonance Cavity Photolysis. Inorg Chem 57:6847-6852
Dong, Min; Kathiresan, Venkatesan; Fenwick, Michael K et al. (2018) Organometallic and radical intermediates reveal mechanism of diphthamide biosynthesis. Science 359:1247-1250
McWilliams, Sean F; Bunting, Philip C; Kathiresan, Venkatesan et al. (2018) Isolation and characterization of a high-spin mixed-valent iron dinitrogen complex. Chem Commun (Camb) 54:13339-13342
Harris, Derek F; Lukoyanov, Dmitriy A; Shaw, Sudipta et al. (2018) Mechanism of N2 Reduction Catalyzed by Fe-Nitrogenase Involves Reductive Elimination of H2. Biochemistry 57:701-710
Seefeldt, Lance C; Hoffman, Brian M; Peters, John W et al. (2018) Energy Transduction in Nitrogenase. Acc Chem Res 51:2179-2186

Showing the most recent 10 out of 51 publications