Chemical control of energy metabolism by N-acyl amino acids

N-酰基氨基酸对能量代谢的化学控制

• 批准号: 10357905
• 负责人: Jonathan Z Long
• 金额: $ 39.88万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-04-01 至 2025-02-28
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10357905
• 关键词: Ablation; Address; Amino Acids; Binding; Binding Proteins; Biochemistry; Biology; Chemicals; Data; Diabetes Mellitus; Disease; Drug Kinetics; Energy Metabolism; Energy Metabolism Pathway; Enzymes; Evaluation; Exhibits; Extracellular Protein; Family; Family member; Fatty Acids; Future; Genetic; Glucose Intolerance; Goals; Health; Homeostasis; Hydrolase; Inner mitochondrial membrane; Insulin Resistance; Lead; Leucine; Ligands; Lipids; Mediating; Medical; Membrane; Metabolic Diseases; Mitochondria; Molecular; Mus; Non-Insulin-Dependent Diabetes Mellitus; Obesity; Obesity Epidemic; Obesity associated disease; Orphan; Outcome; Pathway interactions; Peptide Hydrolases; Persons; Pharmacology; Phenotype; Phenylalanine; Potential Energy; Property; Protons; Public Health; Quality of life; Regulation; Respiration; Testing; Therapeutic; Work; analog; base; blood glucose regulation; combat; crosslink; diet-induced obesity; enzyme activity; experimental study; extracellular; improved; member; metabolomics; mouse model; novel; obesity treatment

We are in the midst of an epidemic of obesity and type 2 diabetes. The discovery of new pathways of energy metabolism is critically needed to address this pressing medical problem. Using untargeted metabolomics, we have identified a new pathway of energy expenditure mediated by family of bioactive lipids called N-acyl amino acids. Certain N-acyl amino acids and stimulate mitochondrial respiration by promoting proton leak. We have also de-orphanized a novel upstream enzyme, PM20D1 (peptidase M20 domain containing 1), that functions as an extracellular N-acyl amino acid synthase/hydrolase. Pharmacological or genetic elevation of circulating N-acyl amino acids increases energy expenditure, reduces adiposity, and improves glucose homeostasis in mouse models of diet-induced obesity. However, we are still early in our understanding of N-acyl amino acids. What remains unknown is how N-acyl amino acids promote proton conductance across the inner mitochondrial membrane, what other extracellular mechanisms regulate N- acyl amino acid levels, and whether this pathway could be useful for the treatment of obesity-associated disorders. Answers are critically needed to understand the biology and therapeutic potential of this energy expenditure pathway in metabolic disease. The long-term goal of this project is to harness energy expenditure pathways for the treatment of obesity and type 2 diabetes. The overall objective of this proposal is to mechanistically dissect the regulators of the N-acyl amino acid pathway and to assess the therapeutic potential of these bioactive lipids. Our central hypothesis is that N-acyl amino acid bioactivity is regulated by both intracellular and extracellular proteins, and that this pathway can be pharmacologically leveraged for the treatment of obesity and type 2 diabetes. We will test this hypothesis via three Specific Aims: 1) Determine how N-acyl amino acids stimulate uncoupled respiration; 2) Determine the mechanisms that control circulating N-acyl amino acid levels; and 3) Evaluate the bioactivity of synthetic N-acyl amino acid analogs in diet-induced obesity mouse models. Successful completion of this proposal will provide a detailed, mechanistic understanding of the regulation and function of N-acyl amino acids in energy metabolism, as well as a pharmacological evaluation of this pathway for the treatment of obesity-associated dis- eases such as type 2 diabetes.

我们正处于肥胖和 2 型糖尿病流行之中。解决这一紧迫的医学问题迫切需要发现新的能量代谢途径。利用非靶向代谢组学，我们发现了一种由称为 N-酰基氨基酸的生物活性脂质家族介导的新的能量消耗途径。某些 N-酰基氨基酸通过促进质子泄漏来刺激线粒体呼吸。我们还去孤儿化了一种新的上游酶 PM20D1（含有 1 的肽酶 M20 结构域），它充当细胞外 N-酰基氨基酸合酶/水解酶。在饮食诱发的肥胖小鼠模型中，循环 N-酰基氨基酸的药理学或遗传升高会增加能量消耗、减少肥胖并改善葡萄糖稳态。然而，我们对 N-酰基氨基酸的了解还处于早期阶段。目前尚不清楚的是，N-酰基氨基酸如何促进穿过线粒体内膜的质子传导，还有哪些其他细胞外机制调节 N-酰基氨基酸水平，以及该途径是否可用于治疗肥胖相关疾病。为了了解代谢疾病中这种能量消耗途径的生物学和治疗潜力，迫切需要答案。该项目的长期目标是利用能量消耗途径来治疗肥胖和 2 型糖尿病。该提案的总体目标是从机械角度剖析 N-酰基氨基酸途径的调节剂并评估这些生物活性脂质的治疗潜力。我们的中心假设是 N-酰基氨基酸生物活性受到细胞内和细胞外蛋白质的调节，并且该途径可以在药理学上用于治疗肥胖和 2 型糖尿病。我们将通过三个具体目标来检验这一假设：1）确定 N-酰基氨基酸如何刺激非偶联呼吸； 2) 确定控制循环N-酰基氨基酸水平的机制； 3) 评估合成 N-酰基氨基酸类似物在饮食诱导的肥胖小鼠模型中的生物活性。该提案的成功完成将为N-酰基氨基酸在能量代谢中的调节和功能提供详细的机制理解，并对该途径治疗2型肥胖相关疾病的药理学评估糖尿病。