Effect of buffer on kinetics of proton equilibration with a protonable group
- PMID: 2990537
- DOI: 10.1021/bi00333a019
Effect of buffer on kinetics of proton equilibration with a protonable group
Abstract
The laser-induced proton pulse generates a massive, brief, proton pulse capable of perturbing biochemical equilibria. The time resolution of the monitoring system can follow the diffusion-controlled protonation of specific sites on macromolecular bodies [Gutman, M. (1984) Methods Biochem. Anal. 30, 1-103]. In order to apply this method in enzymology, one must first evaluate how the buffer capacity of biochemical systems (substrates and proteins) will affect the observed dynamics. Unlike equilibrium measurements, where buffer is an inert component, in kinetic studies buffer modulates the observed dynamics. In this paper we analyze the effect of buffer on the dynamics of protonation in a model system. We describe the experimental technique and introduce the mathematical formalism that determines the various rate constants involved in the reaction. The analysis of the experiments indicates that in buffered solution proton flux is carried by two mechanisms: (A) proton dissociation followed by free proton diffusion; (B) collisional proton transfer between small diffusing solutes. We demonstrate how to evaluate the contribution of each pathway to the overall proton flux.
Similar articles
-
Kinetic analysis of protonation of a specific site on a buffered surface of a macromolecular body.Biochemistry. 1985 Jun 4;24(12):2941-6. doi: 10.1021/bi00333a020. Biochemistry. 1985. PMID: 2990538
-
Kinetic analysis of the protonation of a surface group of a macromolecule.Eur J Biochem. 1983 Jul 15;134(1):63-9. doi: 10.1111/j.1432-1033.1983.tb07531.x. Eur J Biochem. 1983. PMID: 6305658
-
Reaction of bulk protons with a mitochondrial inner membrane preparation: time-resolved measurements and their analysis.Biochemistry. 1993 Mar 30;32(12):2942-6. doi: 10.1021/bi00063a003. Biochemistry. 1993. PMID: 8384483
-
Biophysical aspects of intra-protein proton transfer.Biochim Biophys Acta. 2000 May 12;1458(1):120-34. doi: 10.1016/s0005-2728(00)00063-3. Biochim Biophys Acta. 2000. PMID: 10812028 Review.
-
Protons @ interfaces: implications for biological energy conversion.Biochim Biophys Acta. 2006 Aug;1757(8):913-30. doi: 10.1016/j.bbabio.2006.02.015. Epub 2006 Mar 24. Biochim Biophys Acta. 2006. PMID: 16624250 Review.
Cited by
-
Proton transfer dynamics on the surface of the late M state of bacteriorhodopsin.Biophys J. 2002 Jul;83(1):416-26. doi: 10.1016/S0006-3495(02)75179-5. Biophys J. 2002. PMID: 12080130 Free PMC article.
-
Determination of a unique solution to parallel proton transfer reactions using the genetic algorithm.Biophys J. 2004 Jul;87(1):47-57. doi: 10.1529/biophysj.104.039925. Biophys J. 2004. PMID: 15240443 Free PMC article.
-
Molecular dynamics simulation of proton transport near the surface of a phospholipid membrane.Biophys J. 2002 Mar;82(3):1460-8. doi: 10.1016/S0006-3495(02)75500-8. Biophys J. 2002. PMID: 11867461 Free PMC article.