Inhibition of thiopurine S-methyltransferase activity by impurities in commercially available substrates: a factor for differing results of TPMT measurements

Objectives. Thiopurine S-methyltransferase (TPMT) activity, when measured i n red blood cells (RBC) with a recently published TPMT activity assay using 6-thioguanine (6-TG) as substrate, could not be reproduced in another labo ratory. We investigated factors which could influence the results of the TP MT activity measurement. Methods: We tested twelve 6-TG and four 6-mercaptopurine (6-MP) compounds f rom different suppliers as substrates and determined the enzyme kinetic par ameters K-m and V-max. Furthermore, we studied the influence of different 6 -TG compounds on the affinity of the methyl donor S-adenosyl-L-methionine ( SAM) to the TPMT enzyme. Results: All 6-TG products were of equal purity (declared >98% by the suppl ier); this was ascertained by HPLC. However, the rate of methylation obtain ed following incubation with 6-TG from different suppliers ranged from 10% to 100% when incubated with the same RBC lysate. The lowest apparent K-m va lue for a 6-TG was 22.3 mu mol . l(-1), while the product with the highest methylation rate showed a K-m of 156 mu mol . l(-1) From these results we a ssume that there is a contaminant in some 6-TG products, which acts as a st rong inhibitor of TPMT activity. Compounds possibly used for the synthesis of 6-TG (guanine, pyridine, 6-chloroguanine) did not affect the methylation rate. Thioxanthine, which is known to be a strong inhibitor of TPMT when a dded to the assay system to give a 2% contamination, reduced TPMT activity from 100% to 72%. Using 6-MP from different suppliers as substrate resuited in K-m values ranging from 110 to 162 mu mol . l(-1) and V-max values rang ing from 54 to 68 nmol 6-MMP . g(-1) Hb . h(-1). The K-m value for the meth yl donor SAM was similar to and independent from the thiopurine substrates tested (range 4.9-11 mu mol . l(-1) SAM). In contrast to other investigator s, we found nonenzymatic S-methylation, which was negligible under our assa y conditions (3% with 128 mu mol . l(-1) SAM), but could become relevant in experiments using higher SAM concentrations. Conclusions: TPMT enzyme activity determined with 6-TG as substrate may be strongly inhibited by a contaminant in some of the 6-TG lots distributed.