生物
Cas9
融合蛋白
清脆的
核酸酶
细胞生物学
支架蛋白
计算生物学
绿色荧光蛋白
转录因子
基因表达
基因
分子生物学
遗传学
信号转导
重组DNA
作者
Marvin E. Tanenbaum,Luke A. Gilbert,Lei S. Qi,Jonathan S. Weissman,Ronald D. Vale
出处
期刊:Cell
[Elsevier]
日期:2014-10-01
卷期号:159 (3): 635-646
被引量:1229
标识
DOI:10.1016/j.cell.2014.09.039
摘要
Signals in many biological processes can be amplified by recruiting multiple copies of regulatory proteins to a site of action. Harnessing this principle, we have developed a protein scaffold, a repeating peptide array termed SunTag, which can recruit multiple copies of an antibody-fusion protein. We show that the SunTag can recruit up to 24 copies of GFP, thereby enabling long-term imaging of single protein molecules in living cells. We also use the SunTag to create a potent synthetic transcription factor by recruiting multiple copies of a transcriptional activation domain to a nuclease-deficient CRISPR/Cas9 protein and demonstrate strong activation of endogenous gene expression and re-engineered cell behavior with this system. Thus, the SunTag provides a versatile platform for multimerizing proteins on a target protein scaffold and is likely to have many applications in imaging and controlling biological outputs.
科研通智能强力驱动
Strongly Powered by AbleSci AI