The overall objective of this proposal, using metal-nucleic acid chemistry, is to explore the role of DNA as a polymer in mediating electron transfer reactions. Oligonucleotides will be constructed which contain metal complexes covalently linked to the double helix so as to carry out studies of photoinduced electron transfer between the donor- acceptor pairs on a DNA duplex as a function of DNA length, sequence, and structure. The DNA helix, as a synthetically amenable and structurally well characterized polymer, may be useful (i) fundamentally, in delineating aspects of long range electron transfer processes through pi- stacks, (ii) biologically, towards understanding how radical reactions may damage DNA, and (iii) practically, in the development of biosensors. Oligonucleotides will be constructed which contain a metallointercalating donor or acceptor tethered to the 5'-terminus; dipyridophenazine (dppz) complexes of ruthenium(II) will serve as donors and phenanthrenequinone (phi) complexes of rhodium(III) will serve as electron acceptors. Intercalation of the complexes within the helix will be established through luminescence studies of the ruthenium-modified oligonucleotide base-paired with unmodified complement. The position of intercalation and hence the metal-metal distance on the polymer will be established through photocleavage experiments using the rhodium-modified polymer bound to unlabeled complement. Photoelectron transfer rates between the metal sites on a double strand formed by annealing the rhodium-modified polymer to the ruthenium-modified polymer will be determined through time-resolved luminescence and transient absorption spectroscopy. Preliminary results indicate fast photoelectron transfer over 41 angstrome through the DNA duplex. Oligonucleotides which differ in length intervening between the metal donor and acceptor will be prepared to establish the distance-dependence in electron transfer rate, and sequences will be synthesized which can adopt preferentially the A- or Z-conformations to determine the contribution of base stacking to the electron transfer process. To compare through-bond versus a pi-stack mechanism, electron transfer rates will be compared between double helices of the form (5'-Ru- oligonucleotide-Rh-3'). (3'complement-5') and (5'Ru-oligonucleotide- 3').(3'-complement'Rh-5'). Agents which bind site-specifically to the intervening duplex, such as cis-platin, a restriction enzyme, or an alternate, site-specifically bound rhodium complex, will be employed to examine perturbations in the long-range electron transfer process. A potential DNA-""""""""diode"""""""" will also be constructed to examine whether the incorporation of electron-donating or accepting groups on the helix can impart a """"""""sequence-dependent"""""""" directionality to the electron transfer process.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM049216-01
Application #
3308566
Study Section
Metallobiochemistry Study Section (BMT)
Project Start
1993-03-01
Project End
1996-02-28
Budget Start
1993-03-01
Budget End
1994-02-28
Support Year
1
Fiscal Year
1993
Total Cost
Indirect Cost
Name
California Institute of Technology
Department
Type
Schools of Engineering
DUNS #
078731668
City
Pasadena
State
CA
Country
United States
Zip Code
91125
Grodick, Michael A; Segal, Helen M; Zwang, Theodore J et al. (2014) DNA-mediated signaling by proteins with 4Fe-4S clusters is necessary for genomic integrity. J Am Chem Soc 136:6470-8
Arnold, Anna R; Barton, Jacqueline K (2013) DNA protection by the bacterial ferritin Dps via DNA charge transport. J Am Chem Soc 135:15726-9
Pheeney, Catrina G; Arnold, Anna R; Grodick, Michael A et al. (2013) Multiplexed electrochemistry of DNA-bound metalloproteins. J Am Chem Soc 135:11869-78
Muren, Natalie B; Olmon, Eric D; Barton, Jacqueline K (2012) Solution, surface, and single molecule platforms for the study of DNA-mediated charge transport. Phys Chem Chem Phys 14:13754-71
Sontz, Pamela A; Muren, Natalie B; Barton, Jacqueline K (2012) DNA charge transport for sensing and signaling. Acc Chem Res 45:1792-800
Sontz, Pamela A; Mui, Timothy P; Fuss, Jill O et al. (2012) DNA charge transport as a first step in coordinating the detection of lesions by repair proteins. Proc Natl Acad Sci U S A 109:1856-61
Genereux, Joseph C; Wuerth, Stephanie M; Barton, Jacqueline K (2011) Single-step charge transport through DNA over long distances. J Am Chem Soc 133:3863-8
Olmon, Eric D; Hill, Michael G; Barton, Jacqueline K (2011) Using metal complex reduced states to monitor the oxidation of DNA. Inorg Chem 50:12034-44
Romano, Christine A; Sontz, Pamela A; Barton, Jacqueline K (2011) Mutants of the base excision repair glycosylase, endonuclease III: DNA charge transport as a first step in lesion detection. Biochemistry 50:6133-45
Mui, Timothy P; Fuss, Jill O; Ishida, Justin P et al. (2011) ATP-stimulated, DNA-mediated redox signaling by XPD, a DNA repair and transcription helicase. J Am Chem Soc 133:16378-81

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