PREPARATION OF COMPOUND-SPECIFIC AND GROUP-SPECIFIC ANTIBODIES TO 7-METHYLGUANINE AND RELATED 7-ALKYLGUANINES AND THEIR USE IN IMMUNOAFFINITY PURIFICATION
Mj. Durand et Deg. Shuker, PREPARATION OF COMPOUND-SPECIFIC AND GROUP-SPECIFIC ANTIBODIES TO 7-METHYLGUANINE AND RELATED 7-ALKYLGUANINES AND THEIR USE IN IMMUNOAFFINITY PURIFICATION, Carcinogenesis, 15(5), 1994, pp. 957-961
The preparation and characteristics of compound-specific and group-spe
cific antibodies against 7-alkylguanines (7-alkGua) are described. A c
ompound-specific antibody against 7-methylguanine was prepared using a
hapten bound to carrier protein through the N-2 position. In a compet
itive enzyme-linked immunosorbant assay (ELISA) 7-methylguanine (7-MeG
ua) showed 50% inhibition (I-50%) at 10 pmol/well at room temperature,
but the inhibition was found to be 40 times better at 4 degrees C (I-
50% at 250 fmol/well). When the antibody was bound to protein A-Sephar
ose CL4B 7-MeGua was retained in immunoaffinity columns. A group-speci
fic antibody to 7-alkGua was prepared using 7-(2-carboxy-ethyl)guanine
(7-CEGua) bound to carrier protein via the carboxyl group. In a compe
titive ELISA, this antibody crossreacted well with 7-CEGua, 7-ethylgua
nine (7-EtGua), 7-(2-hydroxyethyl)guanine (7-HOEtGua) and 7-(2',3'-dih
ydroxy)-propylguanine (7-DHPGua) and some inhibition was seen with 7-M
eGua. Immunoaffinity columns prepared from this antibody retained a nu
mber of 7-alkGua of diverse structure. 7-EtGua in calf thymus DNA trea
ted with diethylsulphate and ethylnitrosourea was isolated by immunoaf
finity purification and quantified by HPLC-fluorescence. These results
illustrate the potential of immunoaffinity purification for both indi
vidual DNA adducts and groups of adducts.