PMID:14692765

Citation	Francis, AW, Helquist, SA, Kool, ET and David, SS (2003) Probing the requirements for recognition and catalysis in Fpg and MutY with nonpolar adenine isosteres. J. Am. Chem. Soc. 125:16235-42
Abstract	The Escherichia coli DNA repair enzymes Fpg and MutY are involved in the prevention of mutations resulting from 7,8-dihydro-8-oxo-2'-deoxyguanosine (OG) in DNA. The nonpolar isosteres of 2'-deoxyadenosine, 4-methylbenzimidazole beta-deoxynucleoside (B), and 9-methyl-1H-imidazo[4,5-b]pyridine beta-deoxynucleoside (Q), were used to examine the importance of hydrogen bonding within the context of DNA repair. Specifically, the rate of base removal under single-turnover conditions by the MutY and Fpg glycosylases from duplexes containing OG:B and OG:Q mismatches, relative to OG:A mismatches, was evalulated. The reaction of Fpg revealed a 5- and 10-fold increase in rate of removal of OG from duplexes containing OG:B and OG:Q base pairs, respectively, relative to an OG:A mispair. These results suggest that the lack of the ability to hydrogen bond to the opposite base facilitates removal of OG. In contrast, adenine removal catalyzed by MutY was much more efficient from an OG:A mispair-containing duplex (k2 = 12 +/- 2 min(-1)) compared to the removal of B from an OG:B duplex (k(obs) < 0.002 min(-1)). Surprisingly, MutY was able to catalyze base removal from the OG:Q-containing substrate (k2 = 1.2 +/- 0.2 min(-1)). Importantly, the B and Q analogues are not deleterious to high-affinity DNA binding by MutY. In addition, the B and Q analogues are more susceptible to acid-catalyzed depurination illustrating that the enzyme-catalyzed mechanism is distinct from the nonenzymatic mechanism. Taken together, these results point to the importance of both N7 and N3 in the mechanism of adenine excision catalyzed by MutY.
Links	PubMed Online version:10.1021/ja0374426
Keywords	Adenine/analogs & derivatives; Adenine/chemistry; Adenine/metabolism; Base Pair Mismatch; Catalysis; DNA/chemistry; DNA/metabolism; DNA Glycosylases/chemistry; DNA Glycosylases/metabolism; DNA Repair; DNA-Formamidopyrimidine Glycosylase/chemistry; DNA-Formamidopyrimidine Glycosylase/metabolism; Deoxyguanosine/analogs & derivatives; Deoxyguanosine/chemistry; Deoxyguanosine/metabolism; Escherichia coli Proteins/chemistry; Escherichia coli Proteins/metabolism; Hydrogen Bonding; Hydrogen-Ion Concentration; Imidazoles/chemistry; Imidazoles/metabolism; Kinetics; N-Glycosyl Hydrolases/metabolism; Purine Nucleosides/chemistry; Purine Nucleosides/metabolism; Structure-Activity Relationship
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