INACTIVATION OF BACTERIOPHAGE-T7 DNA-DEPENDENT RNA-POLYMERASE BY 5'-PARA-FLUOROSULFONYLBENZOYLADENOSINE - IDENTIFICATION OF THE MODIFICATION SITE AND THE EFFECT OF THE MODIFICATION ON ENZYME ACTION

Bacteriophage T7 RNA polymerase was covalently modified by 5′‐[4‐fluorosulfonyl)benzoyl]adenosine (4‐FSO2BzAdo). The modified enzyme lacks the ability to catalyze RNA synthesis from the Ø10 promoter of bacteriophage T7; both promoter and GTP binding being markedly decreased. The mild hydrolysis of the ester bond of 4‐FSO2BzAdo within the covalent enzyme‐inhibitor complex restores the RNA synthesis at a lower rate. Sequence studies show that Lys172 is the target of modification by 4‐FSO2BzAdo. This residue, which is situated in the polypeptide region connecting two domains of RNA polymerase, was shown to be the primary site of the limited proteolysis occurring in vivo [Ikeda, R. A. & Richardson, C. C. (1987) J. Biol. Chem. 262, 3790–3799]. We propose that Lys172 is located outside the active site. Once this residue has reacted with 4‐FSO2BzAdo. the nucleoside moiety of the analog is fixed in the NTP‐binding site of the active centre and prevents binding of the substrates. Here, Lys172 per se is not important for the activity but serves as an ‘anchor’ for binding of the inhibitor. Copyright © 1990, Wiley Blackwell. All rights reserved