RT Journal Article SR Electronic T1 Slow Sequential Conformational Changes in Escherichia coli Ribosomes Induced by Lincomycin: Kinetic Evidence JF Molecular Pharmacology JO Mol Pharmacol FD American Society for Pharmacology and Experimental Therapeutics SP 1042 OP 1046 DO 10.1124/mol.56.5.1042 VO 56 IS 5 A1 Sofia Kallia-Raftopoulos A1 Dimitrios L. Kalpaxis YR 1999 UL http://molpharm.aspetjournals.org/content/56/5/1042.abstract AB In a cell-free system derived from Escherichia coli,lincomycin produces biphasic logarithmic time plots for inhibition of peptide-bond formation when puromycin is used as an acceptor substrate and AcPhe-tRNA as a donor substrate. In a previous study, initial slope analysis of the logarithmic time plots revealed that the encounter complex CI between the initiator ribosomal complex (C) and lincomycin (I) undergoes a slow isomerization to C*I. During this change, the bound AcPhe-tRNA and lincomycin are rearranged to also accommodate puromycin, and this may account for the mixed noncompetitive inhibition (K i* = 70 μM) established at higher concentrations of the drug. The above-mentioned effect was further investigated by analyzing the late phase of the logarithmic time plots. It was found that C*I complex reacts with a second molecule of I, giving C*I2 complex. However, the logarithmic time plots remain biphasic even at high concentrations of lincomycin, making possible the identification of another inhibition constantK i*′, which is equal to 18 μM. The simplest explanation of this finding is to assume the existence of a second isomerization step C*I2 ⇌ C*I2 ′, slowly equilibrated. The determination of K i*′ enables us to calculate the isomerization constant (K isom = 2.9) with the formula K i*′ =K i*/(1 + K isom). Our results suggest that whenever a fast and reversible interaction of lincomycin with the elongating ribosomal complex C occurs, the latter undergoes a slow isomerization, which may be the result of conformational changes induced by the drug.