Title | Inhibition of human glutamine synthetase by L-methionine-S,R-sulfoximine-relevance to the treatment of neurological diseases. |
Publication Type | Journal Article |
Year of Publication | 2014 |
Authors | Jeitner TM, Cooper AJL |
Journal | Metab Brain Dis |
Volume | 29 |
Issue | 4 |
Pagination | 983-9 |
Date Published | 2014 Dec |
ISSN | 1573-7365 |
Keywords | Adenosine Triphosphate, Amyotrophic Lateral Sclerosis, Animals, Bacterial Proteins, Convulsants, Dogs, Enzyme Inhibitors, Glutamate-Ammonia Ligase, Humans, Kinetics, Methionine Sulfoximine, Nerve Tissue Proteins, Nervous System Diseases, Plant Proteins, Protein Binding, Recombinant Fusion Proteins, Saccharomyces cerevisiae Proteins, Sheep, Species Specificity |
Abstract | At high concentrations, the glutamine synthetase inhibitor L-methionine-S,R-sulfoximine (MSO) is a convulsant, especially in dogs. Nevertheless, sub-convulsive doses of MSO are neuroprotective in rodent models of hyperammonemia, acute liver disease, and amyotrophic lateral sclerosis and suggest MSO may be clinically useful. Previous work has also shown that much lower doses of MSO are required to produce convulsions in dogs than in primates. Evidence from the mid-20th century suggests that humans are also less sensitive. In the present work, the inhibition of recombinant human glutamine synthetase by MSO is shown to be biphasic-an initial reversible competitive inhibition (K i 1.19 mM) is followed by rapid irreversible inactivation. This K i value for the human enzyme accounts, in part, for relative insensitivity of primates to MSO and suggests that this inhibitor could be used to safely inhibit glutamine synthetase activity in humans. |
DOI | 10.1007/s11011-013-9439-6 |
Alternate Journal | Metab Brain Dis |
PubMed ID | 24136581 |
PubMed Central ID | PMC4180818 |
Grant List | R01 ES008421 / ES / NIEHS NIH HHS / United States R03 NS074286 / NS / NINDS NIH HHS / United States R01 DK016739-22 / DK / NIDDK NIH HHS / United States R01 ES 008421 / ES / NIEHS NIH HHS / United States R03-NS074286 / NS / NINDS NIH HHS / United States |
Related Institute:
Molecular Imaging Innovations Institute (MI3)