| Literature DB >> 34050464 |
Qiaojing Li1, Hideaki Yoshimura2, Takeaki Ozawa1.
Abstract
A split-luciferase-based cell fusion assay enables high-throughput screening of myogenesis-promoting chemicals in chemical libraries. The assay consists of two C2C12 myoblast-derived cell lines (N- and C-cells), each of which stably expresses either an N- or C-terminal split-firefly luciferase (FLuc) fragment fused to a naturally split DnaE intein (N- and C-probes, respectively). The fusion of N- and C-cells during myogenesis induces bioluminescence (BL) in the cytosol due to a stable reconstitution of the split-FLuc. Thus, the myogenesis-promoting effects of a chemical compound can be determined through the enhanced BL intensity. Here, we describe the preparation of N- and C-cells and determination of the myogenesis-promoting effects of imatinib using a 96-well microplate-based assay.Entities:
Keywords: 96-Well microplate-based assay; C2C12 myoblast; Cell fusion; DnaE intein; Firefly luciferase; Imatinib; Myogenesis; Protein splicing; Split luciferase reconstitution
Year: 2021 PMID: 34050464 DOI: 10.1007/978-1-0716-1258-3_8
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745