Chandler Jennifer C, Gandhi Neha S, Mancera Ricardo L, Smith Greg, Elizur Abigail, Ventura Tomer
GenEcology Research Centre, Faculty of Science, Health, Education and Engineering, University of the Sunshine Coast, 4 Locked Bag, Maroochydore, Queensland 4556, Australia.
School of Mathematical Sciences, Queensland University of Technology, 2 George Street, Brisbane, Queensland 4000, Australia.
Int J Mol Sci. 2017 Aug 23;18(9):1832. doi: 10.3390/ijms18091832.
The insulin signalling system is one of the most conserved endocrine systems of from mollusc to man. In decapod , such as the Eastern spiny lobster, (Sv) and the red-claw crayfish, (Cq), insulin endocrinology governs male sexual differentiation through the action of a male-specific, insulin-like androgenic gland peptide (IAG). To understand the bioactivity of IAG it is necessary to consider its bio-regulators such as the insulin-like growth factor binding protein (IGFBP). This work has employed various molecular modelling approaches to represent IGFBP and IAG, along with additional Sv-ILP ligands, in order to characterise their binding interactions. Firstly, we present Sv- and Cq-ILP2: neuroendocrine factors that share closest homology with ILP8 (Dilp8). We then describe the binding interaction of the N-terminal domain of Sv-IGFBP and each ILP through a synergy of computational analyses. In-depth interaction mapping and computational alanine scanning of IGFBP_N' highlight the conserved involvement of the hotspot residues Q, G, D, S, G, G, T and D. The significance of the negatively charged residues D and D was then further exemplified by structural electrostatics. The functional importance of the negative surface charge of IGFBP is exemplified in the complementary electropositive charge on the reciprocal binding interface of all three ILP ligands. When examined, this electrostatic complementarity is the inverse of vertebrate homologues; such physicochemical divergences elucidate towards ligand-binding specificity between Phyla.
胰岛素信号系统是从软体动物到人类最保守的内分泌系统之一。在十足目动物中,如东方多刺龙虾(Sv)和红爪小龙虾(Cq),胰岛素内分泌学通过一种雄性特异性的、胰岛素样的雄激素腺肽(IAG)的作用来控制雄性性别分化。为了理解IAG的生物活性,有必要考虑其生物调节因子,如胰岛素样生长因子结合蛋白(IGFBP)。这项工作采用了各种分子建模方法来表征IGFBP和IAG,以及其他Sv-ILP配体,以确定它们的结合相互作用。首先,我们展示了Sv-和Cq-ILP2:与ILP8(Dilp8)具有最密切同源性的神经内分泌因子。然后,我们通过计算分析的协同作用描述了Sv-IGFBP的N端结构域与每个ILP的结合相互作用。对IGFBP_N'的深入相互作用图谱分析和计算丙氨酸扫描突出了热点残基Q、G、D、S、G、G、T和D的保守参与。然后,通过结构静电学进一步例证了带负电荷的残基D和D的重要性。IGFBP负表面电荷的功能重要性在所有三种ILP配体的相互结合界面上的互补正电荷中得到体现。经检查,这种静电互补性与脊椎动物同源物相反;这种物理化学差异阐明了不同门之间配体结合特异性。