Photolysis of γ-(α-carboxy-2-nitrobenzyl)-L-glutamic acid investigated in the microsecond time scale by time-resolved FTIR

被引:35
作者
Cheng, Q [1 ]
Steinmetz, MG [1 ]
Jayaraman, V [1 ]
机构
[1] Marquette Univ, Dept Chem, Milwaukee, WI 53202 USA
关键词
D O I
10.1021/ja0259988
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The photolytic release of substrates from caged substrates has proven to be an excellent method to generate concentration jumps for kinetic measurements in the microsecond time scale. In this report we use time-resolved FTIR in the step-scan mode to probe the photolysis mechanism of one such caged compound, namely γ-(α-carboxy-2-nitrobenzyl)glutamate, and to obtain a direct measure of the rate of photorelease of the substrate glutamate. The time-resolved difference FTIR spectra exhibit specific signals that can be assigned to the reactant caged glutamate, photolytically released product glutamate, as well as to the aci-nitro intermediate, the key intermediate of the photolysis reaction. Therefore these signals allow the characterization of the kinetics of formation and decay of the intermediate and products. This is the first such report that provides a direct determination of the rate of formation of the photolysis product from a caged compound in the microsecond time scale. Furthermore, the results presented provide a good basis for further time-resolved FTIR studies of molecular reaction mechanisms, such as ligand protein interactions, in the microsecond time scale through the photolytic release of substrates from caged compounds. Copyright © 2002 American Chemical Society.
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页码:7676 / 7677
页数:2
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