Groszmann Michael, De Rosa Annamaria, Chen Weihua, Qiu Jiaen, McGaughey Samantha A, Byrt Caitlin S, Evans John R
Australian Research Council (ARC) Centre of Excellence for Translational Photosynthesis, Research School of Biology, Australian National University, Canberra, ACT, Australia.
Australian Research Council (ARC) Centre of Excellence in Plant Energy Biology, School of Agriculture, Food and Wine, University of Adelaide, Glen Osmond, SA, Australia.
Front Plant Sci. 2023 Jan 19;14:1078220. doi: 10.3389/fpls.2023.1078220. eCollection 2023.
Engineering membrane transporters to achieve desired functionality is reliant on availability of experimental data informing structure-function relationships and intelligent design. Plant aquaporin (AQP) isoforms are capable of transporting diverse substrates such as signaling molecules, nutrients, metalloids, and gases, as well as water. AQPs can act as multifunctional channels and their transport function is reliant on many factors, with few studies having assessed transport function of specific isoforms for multiple substrates.
High-throughput yeast assays were developed to screen for transport function of plant AQPs, providing a platform for fast data generation and cataloguing of substrate transport profiles. We applied our high-throughput growth-based yeast assays to screen all 13 Arabidopsis PIPs (AtPIPs) for transport of water and several neutral solutes: hydrogen peroxide (H2O2), boric acid (BA), and urea. Sodium (Na+) transport was assessed using elemental analysis techniques.
All AtPIPs facilitated water and H2O2 transport, although their growth phenotypes varied, and none were candidates for urea transport. For BA and Na+ transport, AtPIP2;2 and AtPIP2;7 were the top candidates, with yeast expressing these isoforms having the most pronounced toxicity response to BA exposure and accumulating the highest amounts of Na+. Linking putative AtPIP isoform substrate transport profiles with phylogenetics and gene expression data, enabled us to align possible substrate preferences with known and hypothesized biological roles of AtPIPs.
This testing framework enables efficient cataloguing of putative transport functionality of diverse AQPs at a scale that can help accelerate our understanding of AQP biology through big data approaches (e.g. association studies). The principles of the individual assays could be further adapted to test additional substrates. Data generated from this framework could inform future testing of AQP physiological roles, and address knowledge gaps in structure-function relationships to improve engineering efforts.
对膜转运蛋白进行工程改造以实现所需功能,依赖于能够揭示结构 - 功能关系的实验数据以及智能设计。植物水通道蛋白(AQP)亚型能够运输多种底物,如信号分子、营养物质、类金属和气体以及水。AQP可作为多功能通道,其转运功能依赖于许多因素,很少有研究评估特定亚型对多种底物的转运功能。
开发了高通量酵母试验来筛选植物AQP的转运功能,为快速生成数据和编目底物转运谱提供了一个平台。我们应用基于高通量生长的酵母试验,筛选了拟南芥的所有13种质膜内在蛋白(AtPIPs)对水和几种中性溶质的转运:过氧化氢(H2O2)、硼酸(BA)和尿素。使用元素分析技术评估钠(Na +)的转运。
所有AtPIPs都促进了水和H2O2的转运,尽管它们的生长表型有所不同,且没有一个是尿素转运的候选者。对于BA和Na +转运,AtPIP2;2和AtPIP2;7是最佳候选者,表达这些亚型的酵母对BA暴露具有最明显的毒性反应,并且积累的Na +量最高。将推定的AtPIP亚型底物转运谱与系统发育学和基因表达数据联系起来,使我们能够将可能的底物偏好与AtPIPs已知和假设的生物学作用进行比对。
这个测试框架能够高效编目各种AQP的推定转运功能,其规模有助于通过大数据方法(如关联研究)加速我们对AQP生物学的理解。各个试验的原理可以进一步调整以测试其他底物。从这个框架生成的数据可以为未来AQP生理作用的测试提供信息,并填补结构 - 功能关系方面的知识空白,以改进工程研究。