Simultaneous visualization of multiple protein interactions in living cells using multicolor fluorescence complementation analysis
By Chang‐Deng Hu, T. Kerppola. Nature Biotechnology, 2003
802 citations recorded by the source corpus.
Subfields: Biophysics, Cell Biology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/e564dee8f5ac185d745ba434e1fb11902676242b
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Biophysics
- M. Matz
- Sergey A. Lukyanov
- T. Kerppola
- Konstantin A. Lukyanov
- Dmitriy M. Chudakov
- Thomas J. Magliery
- Jason J. Lavinder
- B. Sullivan
In Cell Biology
In Molecular Biology
- T. C. Terwilliger
- M. Matz
- Sergey A. Lukyanov
- T. Kerppola
- Konstantin A. Lukyanov
- Dmitriy M. Chudakov
- Jason J. Lavinder
- Thomas J. Magliery
Citations in the corpus
- Fluorescent proteins and their applications in imaging living cells and tissues. (2010, background): “A very important step forward was the multicolor BiFC assay (179).”
- Visualization of protein interactions in living plant cells using bimolecular fluorescence complementation. (2004, background): “Furthermore, by introducing a large numberof differentGFPvariants the techniquewasextended to multicolor BiFC, which allows the direct visualization of multiple protein interactions within the same cell (Grinberg et al., 2004; Hu and Kerppola, 2003).”
- Bimolecular fluorescence complementation (BiFC) analysis as a probe of protein interactions in living cells. (2008, methodology): “The validity of results from BiFC analysis must be confirmed by examining fluorescence complementation by fusion proteins in which the interaction interface has been mutated (37,45,46).”
- Protein tagging and detection with engineered self-assembling fragments of green fluorescent protein (2005, background): “, but the GFP fragments reported thus far are large and fold poorl”