Conditional control of fluorescent protein degradation by an auxin-dependent nanobody

被引:78
作者
Daniel, Katrin [1 ]
Icha, Jaroslav [2 ,3 ]
Horenburg, Cindy [1 ]
Mueller, Doris [1 ]
Norden, Caren [2 ]
Mansfeld, Joerg [1 ]
机构
[1] Tech Univ Dresden, Biotechnol Ctr, Cell Cycle, Tatzberg 47-49, D-01307 Dresden, Germany
[2] Max Planck Inst Mol Cell Biol & Genet, Pfotenhauerstr 108, D-01307 Dresden, Germany
[3] Univ Turku, Turku Ctr Biotechnol, Tykistokatu 6, FIN-20520 Turku, Finland
基金
欧洲研究理事会;
关键词
ANAPHASE-PROMOTING COMPLEX; NUCLEAR-PORE COMPLEX; DEGRON SYSTEM; GENE-FUNCTION; HUMAN-CELLS; ZEBRAFISH; GFP; DEPLETION; CONSTRUCTION; MICROSCOPY;
D O I
10.1038/s41467-018-05855-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The conditional and reversible depletion of proteins by auxin-mediated degradation is a powerful tool to investigate protein functions in cells and whole organisms. However, its wider applications require fusing the auxin-inducible degron (AID) to individual target proteins. Thus, establishing the auxin system for multiple proteins can be challenging. Another approach for directed protein degradation are anti-GFP nanobodies, which can be applied to GFP stock collections that are readily available in different experimental models. Here, we combine the advantages of auxin and nanobody-based degradation technologies creating an AID-nanobody to degrade GFP-tagged proteins at different cellular structures in a conditional and reversible manner in human cells. We demonstrate efficient and reversible inactivation of the anaphase promoting complex/cyclosome (APC/C) and thus provide new means to study the functions of this essential ubiquitin E3 ligase. Further, we establish auxin degradation in a vertebrate model organism by employing AID-nanobodies in zebrafish.
引用
收藏
页数:13
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