Differences in the rate of repair of O-6-alkylguanines in different sequence contexts by O-6-alkylguanine-DNA alkyltransferase

作者：Coulter Richard; Blandino Maureen; Tomlinson Jessica M; Pauly Gary T; Krajewska Magdalena; Moschel Robert C; Peterson Lisa A; Pegg Anthony E; Spratt Thomas E^*

来源：Chemical Research in Toxicology, 2007, 20(12): 1966-1971.

DOI：10.1021/tx700271j

O-6-Alkylguanine-DNA alkyltransferase (AGT) repairs O-6-alkylguanine residues at different rates depending on the identity of the alkyl group as well as the sequence context. To elucidate the mechanism(s) underlying the differences in rates, we examined the repair of five alkyl groups in three different sequence, contexts. The k(inact) and K-m values were determined by measuring the rates of repair of oligodeoxynucleotide duplexes containing the O-6-alkylguanine residues with various concentrations of AGT in excess. The time course of the reactions all followed pseudo-first-order kinetics except for one of the O-6-ethylguanine substrates, which could be analyzed in a two-phase exponential equation. The differences in rates of repair between the different alkyl groups and the different sequence contexts are dependent on rates of alkyl transfer and not substrate recognition. The relative rates of reaction are in general benzyl > methyl > ethyl > 2-hydroxyethyl > 4-(3-pyridyl)-4-oxobutyl, but the absolute rates are dependent on sequence. The k(inact) values between benzyl and 4-(3-pyridyl)-4-oxobutyl range from 2300 to 350000 depending on sequence. The sequence-dependent variation in k(inact) varied the most for O-6-[4-(3-pyridyl)-4-oxobutyl]guanine, which ranged from 0.022 to 0.000016 s(-1). The results are consistent with a mechanism in which the O-6-alkylguanine can bind to AGT in either a reactive or an unreactive orientation, the proportion of which depends on the sequence context.

• 出版日期2007-12