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Photolabile Precursors of Glutamate: Synthesis, Photochemical Properties, and Activation of Glutamate Receptors on a Microsecond Time Scale
Newly synthesized photolabile derivatives of glutamate, caged glutamate, that release free glutamate on a microsecond time scale after a pulse of UV laser light are described. 2-Nitrobenzyl derivatives were attached to the amino or carboxyl groups of glutamate. Substitution with a -CO- 2group at the...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 1994-09, Vol.91 (19), p.8752-8756 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Newly synthesized photolabile derivatives of glutamate, caged glutamate, that release free glutamate on a microsecond time scale after a pulse of UV laser light are described. 2-Nitrobenzyl derivatives were attached to the amino or carboxyl groups of glutamate. Substitution with a -CO-
2group at the benzylic carbon accelerates the photolysis reaction when compared to -H and -CH3substituents. γ-O-(α-Carboxy-2-nitrobenzyl)glutamate is stable at neutral pH. In 100 mM phosphate buffer at pH 7.0, the compound is photolyzed at 308 nm with a quantum product yield of 0.14. The half-life of the major component of the photolytic reaction, as judged by the transient absorbance change at 430 nm, is 21 μ s (≈90%); the half-life of a minor component (≈10%) is 0.2 ms. The amine-linked derivatives have half-lives in the millisecond region and a 4-fold lower quantum yield. The potential of the newly synthesized compound for use in rapid chemical kinetic investigations of glutamate receptors is demonstrated. (i) The caged glutamate at 1 mM concentration does not desensitize glutamate receptors in rat hippocampal neurons. (ii) Caged glutamate (1 mM) does not inhibit activation of the receptors by 50 μ M glutamate. (iii) Photolysis of the compound induces rapid onset of transmembrane currents in rat hippocampal neurons. |
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ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.91.19.8752 |