Metal ions in biology allow for an expanded chemical repertoire; the local protein environment and metal coordination sphere act synergistically to confer unique reactivity. It is therefore not surprising that the reactions catalyzed by metalloenzymes are chemically challenging and essential for life. We use X-ray crystallography to study the structure and mechanism of complex metallocofactors. Our findings have applications for the synthesis of biomimetic catalysts and in the design of enzyme inhibitors. In addition to investigating the mechanisms of these enzymes, it is also essential to understand the regulation of the levels of the trace minerals required for metallocenter assembly. Here we propose to study the structure and mechanism of enzymes involved in carbon monoxide oxidation and acetyl-CoA synthesis: the Ni requiring carbon monoxide dehydrogenase/acetyl-CoA synthases (CODH/ACS), corrinoid Fe-S protein (CFeSP), methyltetrahydrofolate-CFeSP methyltransferase (MeTr). To explore cellular Ni uptake, we will investigate the structure and mechanism of Ni-regulatory protein NikR. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM069857-01
Application #
6712015
Study Section
Metallobiochemistry Study Section (BMT)
Program Officer
Basavappa, Ravi
Project Start
2004-01-02
Project End
2007-12-31
Budget Start
2004-01-02
Budget End
2004-12-31
Support Year
1
Fiscal Year
2004
Total Cost
$256,314
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Wittenborn, Elizabeth C; Merrouch, Mériem; Ueda, Chie et al. (2018) Redox-dependent rearrangements of the NiFeS cluster of carbon monoxide dehydrogenase. Elife 7:
Nakashige, Toshiki G; Bowman, Sarah E J; Zygiel, Emily M et al. (2018) Biophysical Examination of the Calcium-Modulated Nickel-Binding Properties of Human Calprotectin Reveals Conformational Change in the EF-Hand Domains and His3Asp Site. Biochemistry 57:4155-4164
Chen, Percival Yang-Ting; Aman, Heather; Can, Mehmet et al. (2018) Binding site for coenzyme A revealed in the structure of pyruvate:ferredoxin oxidoreductase from Moorella thermoacetica. Proc Natl Acad Sci U S A 115:3846-3851
Padmanabhan, S; Jost, Marco; Drennan, Catherine L et al. (2017) A New Facet of Vitamin B12: Gene Regulation by Cobalamin-Based Photoreceptors. Annu Rev Biochem 86:485-514
Backman, Lindsey R F; Funk, Michael A; Dawson, Christopher D et al. (2017) New tricks for the glycyl radical enzyme family. Crit Rev Biochem Mol Biol 52:674-695
Nakashige, Toshiki G; Zygiel, Emily M; Drennan, Catherine L et al. (2017) Nickel Sequestration by the Host-Defense Protein Human Calprotectin. J Am Chem Soc 139:8828-8836
Bridwell-Rabb, Jennifer; Drennan, Catherine L (2017) Vitamin B12in the spotlight again. Curr Opin Chem Biol 37:63-70
Gibson, Marcus I; Chen, Percival Yang-Ting; Johnson, Aileen C et al. (2016) One-carbon chemistry of oxalate oxidoreductase captured by X-ray crystallography. Proc Natl Acad Sci U S A 113:320-5
Bowman, Sarah E J; Bridwell-Rabb, Jennifer; Drennan, Catherine L (2016) Metalloprotein Crystallography: More than a Structure. Acc Chem Res 49:695-702
Gibson, Marcus I; Chen, Percival Yang-Ting; Drennan, Catherine L (2016) A structural phylogeny for understanding 2-oxoacid oxidoreductase function. Curr Opin Struct Biol 41:54-61

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