Pusch Lisa-Maria, Riegler-Berket Lina, Oberer Monika, Zimmermann Robert, Taschler Ulrike
Institute of Molecular Biosciences, NAWI Graz, University of Graz, 8010 Graz, Austria.
BioTechMed-Graz, 8010 Graz, Austria.
Metabolites. 2022 Aug 18;12(8):761. doi: 10.3390/metabo12080761.
α/β-hydrolase domain-containing 6 (ABHD6) belongs to the α/β-hydrolase fold superfamily and was originally discovered in a functional proteomic approach designed to discover monoacylglycerol (MAG) hydrolases in the mouse brain degrading the endocannabinoid 2-arachidonoylglycerol. Subsequent studies confirmed that ABHD6 acts as an MAG hydrolase regulating cannabinoid receptor-dependent and -independent signaling processes. The enzyme was identified as a negative modulator of insulin secretion and regulator of energy metabolism affecting the pathogenesis of obesity and metabolic syndrome. It has been implicated in the metabolism of the lysosomal co-factor bis(monoacylglycerol)phosphate and in the surface delivery of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid-type glutamate receptors. Finally, ABHD6 was shown to affect cancer cell lipid metabolism and tumor malignancy. Here, we provide new insights into the experimentally derived crystal structure of ABHD6 and its possible orientation in biological membranes, and discuss ABHD6's functions in health and disease.
含α/β水解酶结构域6(ABHD6)属于α/β水解酶折叠超家族,最初是在一项功能蛋白质组学研究中发现的,该研究旨在寻找小鼠大脑中降解内源性大麻素2-花生四烯酸甘油酯的单酰甘油(MAG)水解酶。随后的研究证实,ABHD6作为一种MAG水解酶,可调节大麻素受体依赖性和非依赖性信号传导过程。该酶被确定为胰岛素分泌的负调节因子以及能量代谢的调节因子,影响肥胖症和代谢综合征的发病机制。它还参与溶酶体辅助因子双(单酰甘油)磷酸酯的代谢以及α-氨基-3-羟基-5-甲基-4-异恶唑丙酸型谷氨酸受体的表面转运。最后,研究表明ABHD6会影响癌细胞的脂质代谢和肿瘤恶性程度。在此,我们对通过实验获得的ABHD6晶体结构及其在生物膜中的可能取向提供了新的见解,并讨论了ABHD6在健康和疾病中的功能。