Briefly, Huh7 cells were lysed in buffer (150 mM KCl, 25 mM Tris pH 7.4, 5 mM EDTA, 0.5 mM DTT, 0.5% NP-40, 9 g ml 1 leupeptin, 9 g ml 1 pepstatin, 10 g ml 1 chymostatin, 3 g ml 1 aprotinin, 1 mM PMSF and 100 U per ml RNase inhibitor) and centrifuged (12,000 g , 30 min, 4 C)
2019;10(Supplement_4):S404-S421
With the aid of X-ray crystallography and site-directed mutagenesis techniques, the roles of GST active site amino acid residues were identified and evaluated [62, 81]
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