SYNTHETIC ANALOGS FOR METAL-CYSTEINE CONTAINING PROTEINS
Project Number2R01GM036308-02
Contact PI/Project LeaderMILLAR, MICHELLE M.
Awardee OrganizationSTATE UNIVERSITY OF NEW YORK AT ALBANY
Description
Abstract Text
Our research objective is to synthesize and fully characterize new types of
metal-thiolate complexes for the purpose of obtaining fundamental
information about the structural, spectroscopic and reactivity properties
of proteins containing metal-cysteine interactions. The metal-cysteine
ligation mode occurs in a wide range of metalloproteins. Our approach is
to use sterically hindered thiolates to create new types of complexes which
mimic some to the more unusual properties exhibited by metal-cysteine
centers in metalloproteins. The rational leading to this approach is
derived from the analogy and the fact that proteins act as sterically bulky
ligands.
Extensive results obtained in our laboratory have demonstrated that these
ligands react with metals: (1) to form monomeric rather than cluster
compounds and (2) to stabilize metals in their higher oxidation states.
Using this approach, we have prepared synthetic analogs (e.g., [Fe(SR)4]-)
for the oxidized form of rubredoxin and synthetic analogs (e.g.,
[Fe4S4(SR)4]-) for the oxidized form of high potential iron-sulfur
proteins. In addition, it is proposed that similar strategies be used to
synthesize analogs for proteins containing: iron (iron-sulfur proteins and
enzymes); copper (blue copper and cytochrome oxidase); nickel
(hydrogenase); and molybdenum (nitrogenase, xanthine oxidase/dehydrogenase,
aldehyde oxidase, sulfite oxidase and nitrate reductase). The reactivity
properties of these compounds will also be investigated.
Chemico-physical studies of these model compounds will be used to achieve a
fundamental understanding of the relationship between the spectroscopic and
the structural and electronic properties of the metal center. In addition,
the spectroscopic parameters determined form a variety of metal-thiolate
model compounds whould be useful to biochemists in their efforts to
identify and distinguish different types of metal-cysteine coordination
modes. A number of spectroscopic techniques will be used to characterize
the compounds including: X-ray crystallography, magnetic susceptibility,
electrochemical, electronic, vibrational, MCD, NMR, ESR, EXAFS and
Mossbauer measurements.
No Sub Projects information available for 2R01GM036308-02
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