Brain and Mind Centre, The University of Sydney, 94 Mallett Street, Camperdown, NSW, 2050, Australia.
Sydney Pharmacy School, Faculty of Medicine and Health, The University of Sydney, NSW, 2006, Australia.
Br J Pharmacol. 2020 Sep;177(18):4275-4295. doi: 10.1111/bph.15188. Epub 2020 Aug 5.
Concatenation of Cys-loop receptor subunits is a commonly used technique to ensure experimental control of receptor assembly. However, we recently demonstrated that widely used constructs did not lead to the expression of uniform pools of ternary and more complex receptors. The aim was therefore to identify viable strategies for designing concatenated constructs that would allow strict control of resultant receptor pools.
Concatenated dimeric, tetrameric, and pentameric α4β2-containing nicotinic ACh (nACh) receptor constructs were designed with successively shorter linker lengths and expressed in Xenopus laevis oocytes. Resulting receptor stoichiometries were investigated by functional analysis in two-electrode voltage-clamp experiments. Molecular dynamics simulations were performed to investigate potential effects of linkers on the 3D structure of concatemers.
Dimeric constructs were found to be unreliable and should be avoided for expression of ternary receptors. By introducing two short linkers, we obtained efficient expression of uniform receptor pools with tetrameric and pentameric constructs. However, linkers should not be excessively short as that introduces strain on the 3D structure of concatemers.
The data demonstrate that design of concatenated Cys-loop receptors requires a compromise between the desire for control of assembly and avoiding introduction of strain on the resulting protein. The overall best strategy was found to be pentameric constructs with carefully optimised linker lengths. Our findings will advance studies of ternary or more complex Cys-loop receptors as well as enabling detailed analysis of how pharmacological agents interact with stoichiometry-specific binding sites.
连接 Cys 环受体亚基是确保受体组装实验控制的常用技术。然而,我们最近证明,广泛使用的构建体并不能导致形成均匀的三元和更复杂的受体池。因此,本研究旨在确定可行的设计策略,以设计出可严格控制受体池的串联构建体。
设计了具有不同长度连接子的串联二聚体、四聚体和五聚体 α4β2 型烟碱型乙酰胆碱 (nACh) 受体构建体,并在非洲爪蟾卵母细胞中进行表达。通过二电极电压钳实验中的功能分析研究了所得受体的化学计量比。进行分子动力学模拟以研究连接子对串联体 3D 结构的潜在影响。
发现二聚体构建体不可靠,不应用于表达三元受体。通过引入两个短连接子,我们成功地表达了具有均匀受体池的四聚体和五聚体构建体。然而,连接子不应过短,因为这会对串联体的 3D 结构造成应变。
数据表明,串联 Cys 环受体的设计需要在组装控制的愿望和避免对所得蛋白质引入应变之间进行权衡。总体而言,最佳策略是使用精心优化的连接子长度的五聚体构建体。我们的研究结果将推进对三元或更复杂 Cys 环受体的研究,并能够详细分析药理学试剂如何与化学计量比特异性结合位点相互作用。