SYNTHETIC ANALOGS FOR METAL-CYSTEINE CONTAINING PROTEINS
Project Number5R01GM036308-07
Former Number5R01GM032526-02
Contact PI/Project LeaderMILLAR, MICHELLE M.
Awardee OrganizationSTATE UNIVERSITY NEW YORK STONY BROOK
Description
Abstract Text
The research objectives are 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; these proteins are
of vast biological and medical significance. The approach is to use
sterically encumbered thiolates to create new types of complexes which
mimic some of the more unusual properties exhibited by metal-cysteine
centers in proteins. The rationale behind this approach comes from the
thought that proteins act as sterically hindered ligands.
Interestingly, there are numerous examples where monomeric, high-valent
metal-cysteine centers are stabilized in proteins under conditions where
simple organic thiolates would interact with metals to form low-valent,
oligomeric species. Results obtained in our laboratory have demonstrated
that sterically encumbered thiolates react with metals: (1) to form
monomeric species, and (2) to stabilize metals in high oxidation states.
Using this approach, we have prepared synthetic analogs for: (1) the
oxidized form of rubredoxin, [Fe(SR)4]1-; (2) the oxidized form of high
potential iron-sulfur proteins, [Fe4S4(SR)4]1-; (3) the molybdenum
containing oxidases, [O=Mo(VI)(SR)4]; (4) the Ni(III) center in
hydrogenases and carbon monoxide dehydrogenase [Ni(SR)4]1-. Additional
compounds have been acquired for which there is, as yet, no direct
biological analogy: [Fe4S4(SR)4]0, [Ru(SR)4(CO)], [Co(SR)4]1-, etc. We
intend to exploit the chemistry of these compounds and to extend this
approach to new challenges.
Chemico-physical studies of these models compounds will be used to achieve
a fundamental understanding of the relationship between the spectroscopic
and electronic properties of the metal center. Moreover, the spectroscopic
parameters determined for a variety of related metal-thiolate model
compounds should be useful to biochemists in their efforts to identify and
distinguish different types of metal-cysteine coordination modes. A number
of spectroscopic techniques are used to characterize the compounds
including: X-ray crystallography, electrochemical, magnetic susceptibility
electronic, vibrational, NMR, ESR, MCD, EXAFS, and Mossbauer measurements.
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Publications
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