Michael P. Stone

Our lab focuses upon chemistry and structural biology of DNA damage, and its role in cancer etiology. We probe chemical rearrangements of initially formed DNA damage, which may alter genotoxic response in cellular DNA. We are particularly interested in the chemistry of agents that alkylate DNA at the N7-dG position; these may re-arrange into chemically reactive apurinic (AP) sites. They also rearrange to formamidopyrmimidine (Fapy-dG) lesions. which exist as a complex mixture of configurational and conformational isomers. We are interested in how DNA repair and replication enzymes process these damage sites in DNA. We utilize a combination NMR spectroscopy and crystallography for structural determination. Both NMR spectroscopy and X-ray crystallography play major roles in our research program. Our laboratory is affiliated with the Vanderbilt Center in Structural Biology. NMR spectroscopy is used to determine the three dimensional structures and dynamics of site-specifically adducted oligodeoxynucleotides in aqueous solution. Crystallographic approaches allow the structural determination of larger biomolecular complexes involving DNA processing enzymes.

Tomar, R., Minko, I.G., Sharma, P., Lei, L., Kellum, A.H., Jr., Egli, M., Iverson, T.M., McCullough, A.M., Lloyd, R.S., & Stone, M.P "Base Excision Repair of the N-(2-deoxy-D-erythro-pentofuranosyl)-urea Lesion by the hNEIL1 Glycosylase." (2023) Nucleic Acids Res. 51, 3754-3769. PMID: 37014002. PMCID: PMC10164570