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University of Montana

Design, Synthesis and Biological Evaluation of a Family of Excitatory Amino Acid Transporter 3 (EAAT3) Preferring Inhibitors

Abstract

dc:description.abstract

<p>This work describes the synthesis and initial characterization of the biological activity of a family of EAAT3 preferring inhibitors, L-&beta;-benzyl aspartate (L-&beta;-BA) and L-&beta;-BA derivatives. L-&beta;-BA and derivatives were initially synthesized in an approximate 2:1 ratio of diasteromers (threo:erythro), using base promoted enolate addition. Kinetic analysis of 3H-D-aspartate uptake into C17.2 cells expressing the hEAATs demonstrated that L-threo-&beta;-BA is the more potent diastereomer (Ki values of 9 µM for EAAT1, 10.0 µM for EAAT2 and 0.8 µM for EAAT3), acts competitively, and exhibits a 10-fold preference for EAAT3 compared to EAAT1 and EAAT2. Electrophysiological recordings of EAAT-mediated currents in Xenopus oocytes further identified L-&beta;-BA as a non-substrate inhibitor. Derivatives of L-&beta;-BA were prepared and characterized for the ability to inhibit 3H-D-aspartate uptake into hEAAT1-3 expressing C17.2 cells. Computational modeling and analysis of structure activity data suggest the area the aromatic moiety of L-&beta;-BA derivatives probe is 1) 3-dimentionally confined, 2) more tolerant of substitutions at the 3 and 5 positions than the 4 position, 3) at least partially distinct from the area probed by L-TBOA and 4) more accessible in the EAAT3 protein than EAAT1 and EAAT2. Computational modeling supports the pharmacological data and lends insight into the selectivity observed with L-&beta;-BA derivatives. Docking studies suggest that H-bonding interactions of L-&beta;-BA derivatives with key residues in the binding site position L-&beta;-BA analogues in a unique manner that is better tolerated in the EAAT3 protein than in the EAAT1 and EAAT2 proteins.</p>

Degree

thesis:*
Name thesis:degree_name
Doctor of Philosophy (PhD)
Grantor dc:publisher
University of Montana
Year
2008

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Mavencamp, Terri Lynn

Subjects

dc:subject × 5

Identifiers

dc:identifier.*
Repository record dc:identifier
https://scholarworks.umt.edu/etd/303
OAI identifier oai:identifier
oai:scholarworks.umt.edu:etd-1322

Chain of custody

source
Harvested from
Montana Technology
Base URL
scholarworks.umt.edu/do/oai/
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Mavencamp, Terri Lynn. Design, Synthesis and Biological Evaluation of a Family of Excitatory Amino Acid Transporter 3 (EAAT3) Preferring Inhibitors. University of Montana, 2008. https://scholarworks.umt.edu/etd/303