Structural and Mechanistic Basis for the Inactivation of Human Ornithine Aminotransferase by (3S,4S)-3-Amino-4-fluorocyclopentenecarboxylic Acid. 2023

Sida Shen, and Arseniy Butrin, and Brett A Beaupre, and Glaucio M Ferreira, and Peter F Doubleday, and Daniel H Grass, and Wei Zhu, and Neil L Kelleher, and Graham R Moran, and Dali Liu, and Richard B Silverman
Department of Chemistry and Center for Developmental Therapeutics, Northwestern University, Evanston, IL 60208, USA.

Ornithine aminotransferase (OAT) is overexpressed in hepatocellular carcinoma (HCC), and we previously showed that inactivation of OAT inhibits the growth of HCC. Recently, we found that (3S,4S)-3-amino-4-fluorocyclopentenecarboxylic acid (5) was a potent inactivator of γ-aminobutyric acid aminotransferase (GABA-AT), proceeding by an enamine mechanism. Here we describe our investigations into the activity and mechanism of 5 as an inactivator of human OAT. We have found that 5 exhibits 10-fold less inactivation efficiency (kinact/KI) against hOAT than GABA-AT. A comprehensive mechanistic study was carried out to understand its inactivation mechanism with hOAT. pKa and electrostatic potential calculations were performed to further support the notion that the α,β-unsaturated alkene of 5 is critical for enhancing acidity and nucleophilicity of the corresponding intermediates and ultimately responsible for the improved inactivation efficiency of 5 over the corresponding saturated analogue (4). Intact protein mass spectrometry and the crystal structure complex with hOAT provide evidence to conclude that 5 mainly inactivates hOAT through noncovalent interactions, and that, unlike with GABA-AT, covalent binding with hOAT is a minor component of the total inhibition which is unique relative to other monofluoro-substituted derivatives. Furthermore, based on the results of transient-state measurements and free energy calculations, it is suggested that the α,β-unsaturated carboxylate group of PLP-bound 5 may be directly involved in the inactivation cascade by forming an enolate intermediate. Overall, compound 5 exhibits unusual structural conversions which are catalyzed by specific residues within hOAT, ultimately leading to an enamine mechanism-based inactivation of hOAT through noncovalent interactions and covalent modification.

UI MeSH Term Description Entries
D008113 Liver Neoplasms Tumors or cancer of the LIVER. Cancer of Liver,Hepatic Cancer,Liver Cancer,Cancer of the Liver,Cancer, Hepatocellular,Hepatic Neoplasms,Hepatocellular Cancer,Neoplasms, Hepatic,Neoplasms, Liver,Cancer, Hepatic,Cancer, Liver,Cancers, Hepatic,Cancers, Hepatocellular,Cancers, Liver,Hepatic Cancers,Hepatic Neoplasm,Hepatocellular Cancers,Liver Cancers,Liver Neoplasm,Neoplasm, Hepatic,Neoplasm, Liver
D009952 Ornithine An amino acid produced in the urea cycle by the splitting off of urea from arginine. 2,5-Diaminopentanoic Acid,Ornithine Dihydrochloride, (L)-Isomer,Ornithine Hydrochloride, (D)-Isomer,Ornithine Hydrochloride, (DL)-Isomer,Ornithine Hydrochloride, (L)-Isomer,Ornithine Monoacetate, (L)-Isomer,Ornithine Monohydrobromide, (L)-Isomer,Ornithine Monohydrochloride, (D)-Isomer,Ornithine Monohydrochloride, (DL)-Isomer,Ornithine Phosphate (1:1), (L)-Isomer,Ornithine Sulfate (1:1), (L)-Isomer,Ornithine, (D)-Isomer,Ornithine, (DL)-Isomer,Ornithine, (L)-Isomer,2,5 Diaminopentanoic Acid
D009953 Ornithine-Oxo-Acid Transaminase A pyridoxal phosphate enzyme that catalyzes the formation of glutamate gamma-semialdehyde and an L-amino acid from L-ornithine and a 2-keto-acid. EC 2.6.1.13. Ornithine Aminotransferase,Ornithine Transaminase,L-Ornithine-2-Oxo-Acid Aminotransferase,L-Ornithine-2-Oxoglutarate Aminotransferase,Ornithine Ketoacid Aminotransferase,Ornithine-2-Ketoglutarate Aminotransferase,Ornithine-Keto-Acid-Transaminase,Ornithine-Ketoacid-Transaminase,Pyrroline-5-Carboxylate Synthase,Aminotransferase, L-Ornithine-2-Oxo-Acid,Aminotransferase, L-Ornithine-2-Oxoglutarate,Aminotransferase, Ornithine,Aminotransferase, Ornithine Ketoacid,Aminotransferase, Ornithine-2-Ketoglutarate,Ketoacid Aminotransferase, Ornithine,L Ornithine 2 Oxo Acid Aminotransferase,L Ornithine 2 Oxoglutarate Aminotransferase,Ornithine 2 Ketoglutarate Aminotransferase,Ornithine Keto Acid Transaminase,Ornithine Ketoacid Transaminase,Ornithine Oxo Acid Transaminase,Pyrroline 5 Carboxylate Synthase,Synthase, Pyrroline-5-Carboxylate,Transaminase, Ornithine,Transaminase, Ornithine-Oxo-Acid
D002264 Carboxylic Acids Organic compounds containing the carboxy group (-COOH). This group of compounds includes amino acids and fatty acids. Carboxylic acids can be saturated, unsaturated, or aromatic. Carboxylic Acid,Acid, Carboxylic,Acids, Carboxylic
D004791 Enzyme Inhibitors Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction. Enzyme Inhibitor,Inhibitor, Enzyme,Inhibitors, Enzyme
D005680 gamma-Aminobutyric Acid The most common inhibitory neurotransmitter in the central nervous system. 4-Aminobutyric Acid,GABA,4-Aminobutanoic Acid,Aminalon,Aminalone,Gammalon,Lithium GABA,gamma-Aminobutyric Acid, Calcium Salt (2:1),gamma-Aminobutyric Acid, Hydrochloride,gamma-Aminobutyric Acid, Monolithium Salt,gamma-Aminobutyric Acid, Monosodium Salt,gamma-Aminobutyric Acid, Zinc Salt (2:1),4 Aminobutanoic Acid,4 Aminobutyric Acid,Acid, Hydrochloride gamma-Aminobutyric,GABA, Lithium,Hydrochloride gamma-Aminobutyric Acid,gamma Aminobutyric Acid,gamma Aminobutyric Acid, Hydrochloride,gamma Aminobutyric Acid, Monolithium Salt,gamma Aminobutyric Acid, Monosodium Salt
D006528 Carcinoma, Hepatocellular A primary malignant neoplasm of epithelial liver cells. It ranges from a well-differentiated tumor with EPITHELIAL CELLS indistinguishable from normal HEPATOCYTES to a poorly differentiated neoplasm. The cells may be uniform or markedly pleomorphic, or form GIANT CELLS. Several classification schemes have been suggested. Hepatocellular Carcinoma,Hepatoma,Liver Cancer, Adult,Liver Cell Carcinoma,Liver Cell Carcinoma, Adult,Adult Liver Cancer,Adult Liver Cancers,Cancer, Adult Liver,Cancers, Adult Liver,Carcinoma, Liver Cell,Carcinomas, Hepatocellular,Carcinomas, Liver Cell,Cell Carcinoma, Liver,Cell Carcinomas, Liver,Hepatocellular Carcinomas,Hepatomas,Liver Cancers, Adult,Liver Cell Carcinomas
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000596 Amino Acids Organic compounds that generally contain an amino (-NH2) and a carboxyl (-COOH) group. Twenty alpha-amino acids are the subunits which are polymerized to form proteins. Amino Acid,Acid, Amino,Acids, Amino

Related Publications

Sida Shen, and Arseniy Butrin, and Brett A Beaupre, and Glaucio M Ferreira, and Peter F Doubleday, and Daniel H Grass, and Wei Zhu, and Neil L Kelleher, and Graham R Moran, and Dali Liu, and Richard B Silverman
November 2004, Biochemistry,
Sida Shen, and Arseniy Butrin, and Brett A Beaupre, and Glaucio M Ferreira, and Peter F Doubleday, and Daniel H Grass, and Wei Zhu, and Neil L Kelleher, and Graham R Moran, and Dali Liu, and Richard B Silverman
July 2019, Journal of the American Chemical Society,
Sida Shen, and Arseniy Butrin, and Brett A Beaupre, and Glaucio M Ferreira, and Peter F Doubleday, and Daniel H Grass, and Wei Zhu, and Neil L Kelleher, and Graham R Moran, and Dali Liu, and Richard B Silverman
March 1990, Journal of medicinal chemistry,
Sida Shen, and Arseniy Butrin, and Brett A Beaupre, and Glaucio M Ferreira, and Peter F Doubleday, and Daniel H Grass, and Wei Zhu, and Neil L Kelleher, and Graham R Moran, and Dali Liu, and Richard B Silverman
September 2015, ACS chemical biology,
Sida Shen, and Arseniy Butrin, and Brett A Beaupre, and Glaucio M Ferreira, and Peter F Doubleday, and Daniel H Grass, and Wei Zhu, and Neil L Kelleher, and Graham R Moran, and Dali Liu, and Richard B Silverman
February 2015, Journal of the American Chemical Society,
Sida Shen, and Arseniy Butrin, and Brett A Beaupre, and Glaucio M Ferreira, and Peter F Doubleday, and Daniel H Grass, and Wei Zhu, and Neil L Kelleher, and Graham R Moran, and Dali Liu, and Richard B Silverman
March 2007, Bioorganic & medicinal chemistry letters,
Sida Shen, and Arseniy Butrin, and Brett A Beaupre, and Glaucio M Ferreira, and Peter F Doubleday, and Daniel H Grass, and Wei Zhu, and Neil L Kelleher, and Graham R Moran, and Dali Liu, and Richard B Silverman
September 1996, Bioorganic & medicinal chemistry,
Sida Shen, and Arseniy Butrin, and Brett A Beaupre, and Glaucio M Ferreira, and Peter F Doubleday, and Daniel H Grass, and Wei Zhu, and Neil L Kelleher, and Graham R Moran, and Dali Liu, and Richard B Silverman
April 1974, The Journal of antibiotics,
Sida Shen, and Arseniy Butrin, and Brett A Beaupre, and Glaucio M Ferreira, and Peter F Doubleday, and Daniel H Grass, and Wei Zhu, and Neil L Kelleher, and Graham R Moran, and Dali Liu, and Richard B Silverman
March 2022, Journal of the American Chemical Society,
Sida Shen, and Arseniy Butrin, and Brett A Beaupre, and Glaucio M Ferreira, and Peter F Doubleday, and Daniel H Grass, and Wei Zhu, and Neil L Kelleher, and Graham R Moran, and Dali Liu, and Richard B Silverman
May 2023, Journal of the American Chemical Society,
Copied contents to your clipboard!