Olszakier Shunit, Hussein Wessal, Heinrich Ronit, Andreyanov Michael, Blau Achinoam, Otor Yara, Schiller Jackie, Kellner Shai, Berlin Shai
Department of Neuroscience, Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 3525433, Israel.
Proc Natl Acad Sci U S A. 2025 May 20;122(20):e2415268122. doi: 10.1073/pnas.2415268122. Epub 2025 May 13.
Genetically encoded calcium indicators (GECIs) have revolutionized the study of cellular calcium signaling, offering powerful tools for real-time optical monitoring of calcium dynamics. Although contemporary GECIs can be targeted to various organelles, there are no means to obtain active and functional GECIs exclusively at interorganellar junctions. To address this gap, we have developed a toolbox of split versions of green and red GECIs designed to reassemble only when the two "halves" come into proximity. We developed split probes to investigate interorganellar connectivity and activity between mitochondria and the ER (via split-MEGIC) or between the plasma membrane and the ER (via split-sf-MEMBER). We employ the various split-sensors to image neural Ca activity in vitro and in vivo and, in the process, identify Mito-ER junctions and calcium activity within individual dendritic spines by use of split-MEGIC.
基因编码钙指示剂(GECIs)彻底改变了细胞钙信号传导的研究,为钙动力学的实时光学监测提供了强大工具。尽管当代GECIs可以靶向各种细胞器,但目前尚无专门在细胞器间连接部位获得有活性且功能正常的GECIs的方法。为了填补这一空白,我们开发了一个工具箱,其中包含绿色和红色GECIs的拆分版本,设计为仅在两个“半体”靠近时重新组装。我们开发了拆分探针来研究线粒体与内质网之间(通过拆分MEGIC)或质膜与内质网之间(通过拆分sf-MEMBER)的细胞器间连接和活性。我们使用各种拆分传感器对体外和体内的神经钙活性进行成像,并在此过程中通过使用拆分MEGIC识别单个树突棘内的线粒体-内质网连接和钙活性。