Centre for Biological Timing, Division of Neuroscience, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PT, UK.
Department of Biomedical Engineering, Columbia University, New York, NY, 10027, USA.
Pflugers Arch. 2023 Dec;475(12):1387-1407. doi: 10.1007/s00424-023-02879-9. Epub 2023 Dec 1.
Animal opsins are light activated G-protein-coupled receptors, capable of optogenetic control of G-protein signalling for research or therapeutic applications. Animal opsins offer excellent photosensitivity, but their temporal resolution can be limited by long photoresponse duration when expressed outside their native cellular environment. Here, we explore methods for addressing this limitation for a prototypical animal opsin (human rod opsin) in HEK293T cells. We find that the application of the canonical rhodopsin kinase (GRK1)/visual arrestin signal termination mechanism to this problem is complicated by a generalised suppressive effect of GRK1 expression. This attenuation can be overcome using phosphorylation-independent mutants of arrestin, especially when these are tethered to the opsin protein. We further show that point mutations targeting the Schiff base stability of the opsin can also reduce signalling lifetime. Finally, we apply one such mutation (E122Q) to improve the temporal fidelity of restored visual responses following ectopic opsin expression in the inner retina of a mouse model of retinal degeneration (rd1). Our results reveal that these two strategies (targeting either arrestin binding or Schiff-base hydrolysis) can produce more time-delimited opsin signalling under heterologous expression and establish the potential of this approach to improve optogenetic performance.
动物视蛋白是光激活的 G 蛋白偶联受体,能够对 G 蛋白信号进行光遗传学控制,用于研究或治疗应用。动物视蛋白具有出色的光敏性,但当它们在其天然细胞环境之外表达时,其光反应持续时间较长,可能会限制其时间分辨率。在这里,我们探索了在 HEK293T 细胞中解决这个问题的方法,该问题针对的是一种典型的动物视蛋白(人视杆蛋白)。我们发现,将经典的视紫红质激酶(GRK1)/视觉阻遏蛋白信号终止机制应用于该问题时,由于 GRK1 表达的普遍抑制作用而变得复杂。通过使用阻遏蛋白的无磷酸化突变体,可以克服这种衰减,尤其是当这些突变体与视蛋白蛋白结合时。我们还表明,针对视蛋白的席夫碱稳定性的点突变也可以减少信号寿命。最后,我们应用了这样的突变(E122Q)来改善在视网膜变性(rd1)小鼠模型的内视网膜异位表达视蛋白后恢复的视觉反应的时间保真度。我们的结果表明,这两种策略(靶向阻遏蛋白结合或席夫碱水解)可以在异源表达下产生更限时的视蛋白信号,并确立了这种方法提高光遗传学性能的潜力。