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探索stargazin V143L突变对AMPA受体:stargazin复合物动力学的影响。

Exploring the impact of the stargazin V143L mutation on the dynamics of the AMPA receptor: stargazin complex.

作者信息

Gouveia Raquel P, Barreto Carlos A V, Melo Rita, Carvalho Ana Luísa, Moreira Irina S

机构信息

Department of Life Sciences, University of Coimbra, Calçada Martim de Freitas, Coimbra, Portugal.

CNC-Center for Neuroscience and Cell Biology, CIBB-Center for Innovative Biomedicine and Biotechnology, University of Coimbra, Coimbra, Portugal.

出版信息

Front Cell Neurosci. 2025 Jan 17;18:1505846. doi: 10.3389/fncel.2024.1505846. eCollection 2024.

Abstract

Stargazin, a transmembrane AMPAR regulatory protein (TARP), plays a crucial role in facilitating the transport of AMPA receptors to the cell surface, stabilising their localisation at synapses and influencing their gating properties. The primary objective of this study was to investigate the effect of the V143L mutation in stargazin, previously linked to intellectual disability, on the interaction between stargazin and AMPA receptors. To achieve this, we conducted a thorough examination of eight distinct molecular dynamics simulations of AMPA receptor-stargazin complexes, each associated with different conductance levels. Through extensive analysis of complex interface structures and dynamics, we revealed that the stargazin V143L mutation had a more pronounced destabilising effect on complexes with lower conductance levels than on the conductive states of the receptor, suggesting a potential association with impaired synaptic transmission in individuals with this mutation.

摘要

促离子型谷氨酸受体γ-8亚基结合蛋白(Stargazin)是一种跨膜AMPA受体调节蛋白(TARP),在促进AMPA受体向细胞表面转运、稳定其在突触处的定位以及影响其门控特性方面发挥着关键作用。本研究的主要目的是探究此前与智力残疾相关的Stargazin中V143L突变对Stargazin与AMPA受体之间相互作用的影响。为实现这一目标,我们对AMPA受体-Stargazin复合物的八个不同分子动力学模拟进行了全面检查,每个模拟都与不同的电导水平相关。通过对复合物界面结构和动力学的广泛分析,我们发现Stargazin V143L突变对低电导水平复合物的去稳定作用比对受体的传导状态更为明显,这表明该突变个体的突触传递受损可能存在潜在关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/500d/11782175/d613e3d5b18b/fncel-18-1505846-g001.jpg

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