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

被引:77
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
相关论文
共 44 条
[1]   RAC-tagging: Recombineering And Cas9-assisted targeting for protein tagging and conditional analyses [J].
Baker, Oliver ;
Gupta, Ashish ;
Obst, Mandy ;
Zhang, Youming ;
Anastassiadis, Konstantinos ;
Fu, Jun ;
Stewart, A. Francis .
SCIENTIFIC REPORTS, 2016, 6
[2]   Forces Driving Epithelial Spreading in Zebrafish Gastrulation [J].
Behrndt, Martin ;
Salbreux, Guillaume ;
Campinho, Pedro ;
Hauschild, Robert ;
Oswald, Felix ;
Roensch, Julia ;
Grill, Stephan W. ;
Heisenberg, Carl-Philipp .
SCIENCE, 2012, 338 (6104) :257-260
[3]  
Broers JLV, 1999, J CELL SCI, V112, P3463
[4]   Fluorescent fusion protein knockout mediated by anti-GFP nanobody [J].
Caussinus, Emmanuel ;
Kanca, Oguz ;
Affolter, Markus .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2012, 19 (01) :117-U142
[5]   Construction of a cyclin D1-Cdk2 fusion protein to model the biological functions of cyclin D1-Cdk2 complexes [J].
Chytil, A ;
Waltner-Law, M ;
West, R ;
Friedman, D ;
Aakre, M ;
Barker, D ;
Law, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (46) :47688-47698
[6]   A Method for the Acute and Rapid Degradation of Endogenous Proteins [J].
Clift, Dean ;
McEwan, William A. ;
Labzin, Larisa I. ;
Konieczny, Vera ;
Mogessie, Binyam ;
James, Leo C. ;
Schuh, Melina .
CELL, 2017, 171 (07) :1692-+
[7]   Ki-67 acts as a biological surfactant to disperse mitotic chromosomes [J].
Cuylen, Sara ;
Blaukopf, Claudia ;
Politi, Antonio Z. ;
Mueller-Reichert, Thomas ;
Neumann, Beate ;
Poser, Ina ;
Ellenberg, Jan ;
Hyman, Anthony A. ;
Gerlich, Daniel W. .
NATURE, 2016, 535 (7611) :308-+
[8]  
Fridy PC, 2014, NAT METHODS, V11, P1253, DOI [10.1038/nmeth.3170, 10.1038/NMETH.3170]
[9]   A map of protein dynamics during cell-cycle progression and cell-cycle exit [J].
Gookin, Sara ;
Min, Mingwei ;
Phadke, Harsha ;
Chung, Mingyu ;
Moser, Justin ;
Miller, Iain ;
Carter, Dylan ;
Spencer, Sabrina L. .
PLOS BIOLOGY, 2017, 15 (09)
[10]   Inducible, reversible system for the rapid and complete degradation of proteins in mammalian cells [J].
Holland, Andrew J. ;
Fachinetti, Daniele ;
Han, Joo Seok ;
Cleveland, Don W. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (49) :E3350-E3357