Computational and structural evidence for neurotransmitter-mediated modulation of the oligomeric states of human insulin in storage granules

0476143 - ÚOCHB 2018 RIV US eng J - Článek v odborném periodiku
Palivec, Vladimír - Viola, C. M. - Kozak, M. - Ganderton, T. R. - Křížková, Květoslava - Turkenburg, J. P. - Halušková, Petra - Žáková, Lenka - Jiráček, Jiří - Jungwirth, Pavel - Brzozowski, A. M.
Computational and structural evidence for neurotransmitter-mediated modulation of the oligomeric states of human insulin in storage granules.
Journal of Biological Chemistry. Roč. 292, č. 20 (2017), s. 8342-8355. ISSN 0021-9258. E-ISSN 1083-351X
Grant CEP: GA ČR(CZ) GA16-01074S
Institucionální podpora: RVO:61388963
Klíčová slova: insulin * serotonin * dopamine * molecular dynamics * crystallography * spectroscopy
Obor OECD: Biochemistry and molecular biology
Impakt faktor: 4.011, rok: 2017
http://www.jbc.org/content/292/20/8342.full

Human insulin is a pivotal protein hormone controlling metabolism, growth, and aging and whose malfunctioning underlies diabetes, some cancers, and neurodegeneration. Despite its central position in human physiology, the in vivo oligomeric state and conformation of insulin in its storage granules in the pancreas are not known. In contrast, many in vitro structures of hexamers of this hormone are available and fall into three conformational states: T-6, T3R3f, and R-6. As there is strong evidence for accumulation of neurotransmitters, such as serotonin and dopamine, in insulin storage granules in pancreatic beta-cells, we probed by molecular dynamics (MD) and protein crystallography (PC) if these endogenous ligands affect and stabilize insulin oligomers. Parallel studies independently converged on the observation that serotonin binds well within the insulin hexamer (site I), stabilizing it in the T3R3 conformation. Both methods indicated serotonin binding on the hexamer surface (site III) as well. MD, but not PC, indicated that dopamine was also a good site III ligand. Some of the PC studies also included arginine, which may be abundant in insulin granules upon processing of pro-insulin, and stable T3R3 hexamers loaded with both serotonin and arginine were obtained. The MD and PC results were supported further by in solution spectroscopic studies with R-state-specific chromophore. Our results indicate that the T3R3 oligomer is a plausible insulin pancreatic storage form, resulting from its complex interplay with neurotransmitters, and pro-insulin processing products. These findings may have implications for clinical insulin formulations.
Trvalý link: http://hdl.handle.net/11104/0272675