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    Excited state electronic properties of DNA photolyase and fluorescent nucleobase analogues (FBA): An experimental and theoretical study

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    Genre
    Thesis/Dissertation
    Date
    2009
    Author
    Kodali, Goutham
    Advisor
    Stanley, Robert J.
    Committee member
    Nicholson, Allen W.
    Matsika, Spiridoula
    Schelvis, Johannes Petrus Maria, 1966-
    Department
    Chemistry
    Subject
    Chemistry, Physical
    Chemistry, Biochemistry
    Chemistry, General
    Dna
    Dna Photolyase
    Fba
    Flavins
    Fluorescent Nucleobase Analogues
    Stark Spectroscopy
    Permanent link to this record
    http://hdl.handle.net/20.500.12613/1645
    
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    DOI
    http://dx.doi.org/10.34944/dspace/1627
    Abstract
    An overexposure to ultraviolet radiation can cause sunburn and some forms of skin cancer. UV light causes many different photoproducts. The cys-syn cyclobutylpyrimidine dimer (CPD) is the major photoproduct upon UV irradiation. DNA photolyase (PL) is a light-driven flavoprotein that repairs CPD in UV-damaged DNA. This repair process occurs in the presence of blue light through ultrafast photo-induced electron transfer from reduced anionic flavin adenine dinucleotide (FADH¯) to the CPD by an unknown mechanism. Since the excited state flavin transfers an electron to repair the damaged DNA, it is of utmost importance that we understand better the excited state properties of the flavins. In this work the excited state electronic properties of all three-oxidation states of flavin: oxidized form (FAD), semiquinone radical form (FADH•) and reduced anionic form (FADH¯) were studied using Stark spectroscopy and complimented by time dependent density functional theory (TD-DFT) calculations. These results are presented and discussed in Chapter 3 and 4. The difference dipole moments (Δμ) and the difference polarizabilities (Tr(Δα01)) were experimentally determined for first two lowest optically accessible states. The results are discussed in the context of photoreduction of flavins in wider class of flavoprotein blue light photoreceptors and catalytic electron transfer process in DNA repair. In the later part of this thesis (Chapters 5 and 6) the excited state electronic properties of monomeric 2-Aminopurine (2AP), 8-Vinyladenine 8VA were presented. These 8VA, 2AP are examples of fluorescent nucleotide analogues of adenine that can be incorporated into DNA with little perturbation of the normal double-helical structure. The fluorescence of these analogues is quenched when incorporated in double-stranded DNA (dsDNA). The basic mechanism underlying the fluorescence quenching by base stacking of 2AP and 8VA are is not well understood, and thus exploring the excited state electronic structures of these bases is an important first step. We have explored the excited state properties of 2AP and 8VA in frozen LiCl and ethanol solutions using Stark spectroscopy. High-level ab initio and TD-DFT calculations were performed to compliment the experimental results.
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