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在经过压力抛光的斑马鱼绿锥细胞贴片电极中加入光转导蛋白。

Incorporating phototransduction proteins in zebrafish green cone with pressure-polished patch pipettes.

机构信息

Department of Biomedical and Specialized Surgical Sciences, Section of Physiology, Via Borsari 46, I-44121 Ferrara, Italy.

Department of Neurosciences, Biomedicine and Movement Sciences, Section of Biological Chemistry, University of Verona, Strada le Grazie 8, I-37124 Verona, Italy.

出版信息

Biophys Chem. 2019 Oct;253:106230. doi: 10.1016/j.bpc.2019.106230. Epub 2019 Jul 22.

Abstract

The neuronal Ca-sensor guanylate cyclase-activating protein 3 (zGCAP3) is a major regulator of guanylate cyclase (GC) activity expressed in zebrafish cone cells. Here, the zGCAP3, or a monoclonal antibody directed against zGCAP3, was injected in the cone cytoplasm by employing the pressure-polished pipette technique. This technique allows to perform "real time" zGCAP3 (or of any other phototransduction protein) over-expression or knock-down, respectively, via the patch pipette. Photoresponses were not affected by purified zGCAP3, indicating that GC was already saturated with endogenous zGCAP3. The cytosolic injection of anti-zGCAP3 produced the slowing down kinetics of the flash response recovery, as theoretically expected by a minimal phototransduction model considering the antibody acting exclusively on the maximal GC activation by low Ca. However, the antibody produced a progressive current decay toward the zero level, as if the antibody affected also the basal GC activity in the dark.

摘要

神经元钙传感器鸟苷酸环化酶激活蛋白 3(zGCAP3)是斑马鱼视锥细胞中鸟苷酸环化酶(GC)活性的主要调节剂。在这里,通过使用抛光压管技术将 zGCAP3 或针对 zGCAP3 的单克隆抗体注射到视锥细胞质中。该技术允许通过贴片管分别进行“实时”zGCAP3(或任何其他光转导蛋白)的过表达或敲低。光反应不受纯化的 zGCAP3 的影响,表明 GC 已经被内源性 zGCAP3 饱和。细胞质内注射抗 zGCAP3 会导致闪光反应恢复的动力学减慢,这与考虑抗体仅通过低钙对最大 GC 激活起作用的最小光转导模型理论上的预期一致。然而,抗体产生了朝向零水平的渐进电流衰减,就好像抗体也影响了黑暗中基础 GC 的活性。

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