Arai Yoshiyuki, Nagai Takeharu
The Institute of Scientific and Industrial Research, Osaka University, Osaka, Japan.
Curr Protoc Chem Biol. 2014 Dec 1;6(4):221-236. doi: 10.1002/9780470559277.ch140168.
Chemiluminescence imaging can be performed without excitation light sources at various spatial levels ranging from a single cell to the whole body. Thus far, chemiluminescence imaging has been primarily performed with long exposure times because of weak signals, resulting in low temporal resolution. Recently, the brightest-known chemiluminescent proteins--Nano-lantern and Nano-lantern-based functional indicators--have been developed. Nano-lantern probes break the limitation of temporal resolution and enable chemiluminescence imaging of living samples such as cells, plants, and small animals at video rates. This unit describes one protocol for observation of a freely moving unshaved mouse transplanted with Nano-lantern-expressing tumor cells, and another for compatible use of optogenetic tools and a Nano-lantern calcium indicator. Both protocols utilize the synchronization of illumination and camera acquisition sessions, thereby enabling real-time chemiluminescence imaging.
化学发光成像可以在没有激发光源的情况下在从单细胞到整个身体的各种空间水平上进行。到目前为止,由于信号较弱,化学发光成像主要是在长时间曝光下进行的,导致时间分辨率较低。最近,已经开发出了已知最亮的化学发光蛋白——纳米灯笼和基于纳米灯笼的功能指示剂。纳米灯笼探针打破了时间分辨率的限制,能够以视频速率对细胞、植物和小动物等活样本进行化学发光成像。本单元描述了一种观察移植了表达纳米灯笼的肿瘤细胞的自由活动未剃毛小鼠的方案,以及另一种用于光遗传学工具和纳米灯笼钙指示剂兼容使用的方案。这两种方案都利用了照明和相机采集会话的同步,从而实现实时化学发光成像。