Differential specificity of monochlorobimane for isozymes of human and rodent glutathione S-transferases

• Published in: Cancer research (Chicago, Ill.) Vol. 51; no. 6; pp. 1606 - 1612
• Main Authors: COOK, J. A, IYPE, S. N, MITCHELL, J. B
• Format: Journal Article
• Language: English
• Published: Philadelphia, PA American Association for Cancer Research 15.03.1991
• Subjects: Analytical, structural and metabolic biochemistry; Animals; Biological and medical sciences; Biomarkers; Enzymes and enzyme inhibitors; Flow Cytometry; Fluorescent Dyes - metabolism; Fundamental and applied biological sciences. Psychology; Glutathione - metabolism; Glutathione Transferase - analysis; Humans; Isoenzymes - analysis; Kinetics; Pyrazoles - metabolism; Rats; Species Specificity; Substrate Specificity; Transferases; Tumor Cells, Cultured; Human; Cell culture; Flow cytometry; Rat; Enzyme; Isozyme; Rodentia; HPLC chromatography; Fluorescence; Species specificity; Probe; In vitro; Vertebrata; Mammalia; Investigation method; Michaelis constant; Glutathione transferase; Animal; Kinetics; Tumor cell; Comparative study; Quantitative analysis
• ISSN: 0008-5472; 1538-7445

Monochlorobimane (MCB) has been used as a glutathione (GSH) specific fluorescent probe capable of delineating GSH heterogeneity in cellular systems. Generally, low concentrations of MCB (less than 50 microM) have been used to quantitatively label GSH in rodent cell lines. Incubation of the hamster cell lines, CHO AB1 and V79, with 10 microM MCB labeled 75 and 39% of the reduced GSH pool, respectively. In contrast, incubation of 7 different human cell lines with 10 microM MCB labeled less than 4% of the total reduced GSH pool. The human cell lines required 1000 microM MCB to label an average of 73% of the GSH pool (range, 60-88%). When using 1000 microM MCB to label GSH, flow cytometry results from 7 different cell lines (human and rodent) were in good agreement with high performance liquid chromatography and standard spectrophotometric analysis with regards to a rank ordering of the GSH content determined for each cell line. The human glutathione S-transferases B2B2, B1B2, psi, pi, and the rat transferases 1-2, 3-3, and 3-4 were isolated and purified for steady state kinetic analysis with MCB and GSH as the primary substrates. The human basic transferases, B1B2 and B2B2, had Km values for MCB of 354 and 283 microM and Vmax values of 33.3 and 34.6 mumol bimane-GSH/min/mg protein, respectively. The rat basic transferase 1-2 showed similar kinetic results with a Km of 199 microM and a Vmax of 35.5 mumol bimane-GSH/min/mg protein. The human neutral transferase (psi) had a Km for MCB of 204 microM with a Vmax of 6.5 mumol bimane-GSH/min/mg protein. In contrast, MCB has a high affinity for the rat neutral transferase with a Km of 2.6 microM and a Vmax of 35.1 mumol bimane-GSH/min/mg protein. The human acidic transferase (pi), the predominate transferase found in most human tumor cell lines, has a Km of 264 microM for MCB and a Vmax of 1.99 mumol bimane-GSH/min/mg protein. The kcat/Km values indicated that MCB is an excellent substrate for the rat neutral transferases while the human pi glutathione S-transferase showed the least reactivity. Collectively the data indicate that MCB fails to label GSH at lower concentrations (less than 50 microM) in human cell lines because of the reduced affinity of MCB for the human transferases and possibly also due to differences in glutathione S-transferase isozyme expression between rodent and human cell lines.