Thermodynamic and Kinetic Stabilities of Active Site Protonation States of Class C 尾-Lactamase

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• 作者：Ravi Tripathi ; Nisanth N. Nair
• 刊名：The Journal of Physical Chemistry B
• 出版年：2012
• 出版时间：April 26, 2012
• 年：2012
• 卷：116
• 期：16
• 页码：4741-4753
• 全文大小：708K
• 年卷期：v.116,no.16(April 26, 2012)
• ISSN：1520-5207

文摘

By employing computationally intensive molecular dynamics simulations using hybrid quantum鈥搈echanical/molecular鈥搈echanical approach, we analyze here the kinetic and thermodynamic stabilities of various active site protonation states of a fully solvated class C 尾-lactamase. We report the detailed mechanism of proton transfer between catalytically important active site residues and the associated free energy barriers. In the apoenzyme, significant structural changes are associated with the proton transfer, and the orientations of active site residues are distinctly different for various protonation states. Among several propositions on the protonation state of the apoprotein, we find that the one with Tyr₁₅₀ deprotonated and both Lys₆₇ and Lys₃₁₅ residues being protonated is the most stable one, both thermodynamically and kinetically. However, the equilibrium structure at room temperature is a dynamic one, with Lys₃₁₅H_味 delocalized between Tyr₁₅₀O_畏 and Lys₃₁₅N_味. Of great importance, the kinetic and thermodynamic stability of protonation states are significantly affected on noncovalently complexing with cephalothin, an antibiotic molecule. The equilibrium structure of the enzyme鈥搒ubstrate (precovalent) complex has a dynamic protonation state where a proton shuttles frequently between the Tyr₁₅₀O_畏 and Lys₆₇N_味. We examine here the genesis of the manifold change in stability at the molecular level. The importance of our observations toward understanding the reactivity of the enzyme is discussed and experimental observations are rationalized.