荧光素酶
蛋白质片段互补分析
互补
荧光素
原生质体
化学
植物细胞
转染
细胞
细胞生物学
生物化学
生物
基因
突变体
作者
Jian‐Feng Li,Dandan Zhang
标识
DOI:10.1002/0471142727.mb2009s107
摘要
This unit describes the split firefly luciferase complementation (SFLC) assay, a high-throughput quantitative method that can be used to investigate protein-protein interactions (PPIs) in plant mesophyll protoplasts. In SFLC, the two proteins to be tested for interaction are expressed as chimeric proteins, each fused to a different half of firefly luciferase. If the proteins interact, a functional luciferase can be transitorily reconstituted, and is detected using the cell-permeable substrate D-luciferin. An advantage of the SFLC assay is that dynamic changes in PPIs in a cell can be detected in a near real-time manner. Another advantage is the unusually high DNA co-transfection and protein expression efficiencies that can be achieved in plant protoplasts, thereby enhancing the throughput of the method.
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