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Tom K. Kerppola

University of Michigan

ORCID: 0000-0002-0611-9446

Publishes on Genomics and Chromatin Dynamics, Ubiquitin and proteasome pathways, RNA and protein synthesis mechanisms. 99 papers and 11.8k citations.

99Publications
11.8kTotal Citations

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Top publicationsby citations

Bimolecular Fluorescence Complementation (BiFC) Analysis as a Probe of Protein Interactions in Living Cells
Tom K. Kerppola|Annual Review of Biophysics|2008
Cited by 711Open Access

Protein interactions are a fundamental mechanism for the generation of biological regulatory specificity. The study of protein interactions in living cells is of particular significance because the interactions that occur in a particular cell depend on the full complement of proteins present in the cell and the external stimuli that influence the cell. Bimolecular fluorescence complementation (BiFC) analysis enables direct visualization of protein interactions in living cells. The BiFC assay is based on the association between two nonfluorescent fragments of a fluorescent protein when they are brought in proximity to each other by an interaction between proteins fused to the fragments. Numerous protein interactions have been visualized using the BiFC assay in many different cell types and organisms. The BiFC assay is technically straightforward and can be performed using standard molecular biology and cell culture reagents and a regular fluorescence microscope or flow cytometer.