Visualization of interactions among bZIP and Rel family proteins in living cells using bimolecular fluorescence complementation.
By Chang‐Deng Hu, Yurii Chinenov, T. Kerppola. Molecules and Cells, 2002
1,582 citations recorded by the source corpus.
Subfields: Biophysics, Cell Biology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/5470fb9b5e1b57ce73916fb94064fcc34ac7adbe
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In Biophysics
- A. Visser
- Jan Willem Borst
- Thomas J. Magliery
- Jason J. Lavinder
- B. Sullivan
- M. Matz
- Sergey A. Lukyanov
- M. Sheetz
In Cell Biology
- A. Visser
- Jan Willem Borst
- Thomas J. Magliery
- Jason J. Lavinder
- B. Sullivan
- M. Matz
- Sergey A. Lukyanov
- M. Sheetz
In Molecular Biology
- A. Visser
- Jan Willem Borst
- S. Dinesh-Kumar
- Michael Schiff
- Jason J. Lavinder
- Thomas J. Magliery
- B. Sullivan
- José M. Alonso
Citations in the corpus
- Force sensing by mechanical extension of the Src family kinase substrate p130Cas. (2006, background): “When the two halves of a split YFP, YFP-N and YFP-C, were fused to the aminoand carboxy-terminal ends of NC-biotinylated CasSD, respectively (NY/CY-NC-biotinylated CasSD, Figure 3B), we observed yellow fluorescence in both NY/CY-NC-biotinylated CasSD-expressing bacteria and the purified protein, as ”
- Split-Cre Complementation Indicates Coincident Activity of Different Genes In Vivo (2009, background): “However, fluorescent protein complementation still constitutes only a transient signal [27].”
- Fluorescence lifetime imaging microscopy in life sciences (2010, methodology): “When two potentially interacting proteins, fused to two complementing GFP fragments, are in close proximity, the proteins can bring the N- and C-terminal GFP domains into a favourable position and orientation and thereby facilitate their association into a functional fluorophore [84, 85].”
- The interplay between the glucocorticoid receptor and nuclear factor-kappaB or activator protein-1: molecular mechanisms for gene repression. (2003, background): “] with respect to its cofactor partners (274, 392, 457, 458).”
- Direct observation of individual endogenous protein complexes in situ by proximity ligation (2006, methodology): “In contrast, techniques such as bimolecular fluorescence complementatio”
- A Novel Role for the TIR Domain in Association with Pathogen-Derived Elicitors (2007, methodology): “BiFC does not require that the associating proteins make direct contact with each other and therefore cannot distinguish between direct and indirect associations [40].”