A new protein-protein interaction sensor based on tripartite split-GFP association.
A new protein-protein interaction sensor based on tripartite split-GFP association.
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DOI:
10.1038/srep02854
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发表时间:
2013-10-04
影响因子:
4.6
通讯作者:
Waldo, Geoffrey S.
中科院分区:
文献类型:
--
作者:
Cabantous, Stephanie;Nguyen, Hau B.;Pedelacq, Jean-Denis;Koraichi, Faten;Chaudhary, Anu;Ganguly, Kumkum;Lockard, Meghan A.;Favre, Gilles;Terwilliger, Thomas C.;Waldo, Geoffrey S.
Monitoring protein-protein interactions in living cells is key to unraveling their roles in numerous cellular processes and various diseases. Previously described split-GFP based sensors suffer from poor folding and/or self-assembly background fluorescence. Here, we have engineered a micro-tagging system to monitor protein-protein interactions in vivo and in vitro. The assay is based on tripartite association between two twenty amino-acids long GFP tags, GFP10 and GFP11, fused to interacting protein partners, and the complementary GFP1-9 detector. When proteins interact, GFP10 and GFP11 self-associate with GFP1-9 to reconstitute a functional GFP. Using coiled-coils and FRB/FKBP12 model systems we characterize the sensor in vitro and in Escherichia coli. We extend the studies to mammalian cells and examine the FK-506 inhibition of the rapamycin-induced association of FRB/FKBP12. The small size of these tags and their minimal effect on fusion protein behavior and solubility should enable new experiments for monitoring protein-protein association by fluorescence.
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DOI:
10.1093/protein/gzr021
发表时间:
2011-07
期刊:
Protein engineering, design & selection : PEDS
影响因子:
--
作者:
Lockard MA;Listwan P;Pedelacq JD;Cabantous S;Nguyen HB;Terwilliger TC;Waldo GS
通讯作者:
Waldo GS
影响因子:
46.9
作者:
Galarneau, A;Primeau, M;Michnick, SW
通讯作者:
Michnick, SW
影响因子:
15
作者:
Magliery, TJ;Wilson, CGM;Regan, L
通讯作者:
Regan, L
影响因子:
14.9
作者:
Pedelacq, Jean-Denis;Nguyen, Hau B.;Waldo, Geoffrey S.
通讯作者:
Waldo, Geoffrey S.
DOI:
10.1073/pnas.94.16.8405
发表时间:
1997-08-05
影响因子:
11.1
作者:
Rossi, F;Charlton, CA;Blau, HM
通讯作者:
Blau, HM