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Protein- protein interaction detection system using fluorescent protein microdomains

Patent ·
OSTI ID:1014181
The invention provides a protein labeling and interaction detection system based on engineered fragments of fluorescent and chromophoric proteins that require fused interacting polypeptides to drive the association of the fragments, and further are soluble and stable, and do not change the solubility of polypeptides to which they are fused. In one embodiment, a test protein X is fused to a sixteen amino acid fragment of GFP (.beta.-strand 10, amino acids 198-214), engineered to not perturb fusion protein solubility. A second test protein Y is fused to a sixteen amino acid fragment of GFP (.beta.-strand 11, amino acids 215-230), engineered to not perturb fusion protein solubility. When X and Y interact, they bring the GFP strands into proximity, and are detected by complementation with a third GFP fragment consisting of GFP amino acids 1-198 (strands 1-9). When GFP strands 10 and 11 are held together by interaction of protein X and Y, they spontaneous association with GFP strands 1-9, resulting in structural complementation, folding, and concomitant GFP fluorescence.
Research Organization:
Los Alamos National Security, LLC (Los Alamos, NM)
Sponsoring Organization:
USDOE
DOE Contract Number:
W-7405-ENG-36
Assignee:
Los Alamos National Security, LLC (Los Alamos, NM)
Patent Number(s):
7,666,606
Application Number:
US Patent Application 11/295,368
OSTI ID:
1014181
Country of Publication:
United States
Language:
English

References (7)

Visualization of Interactions among bZIP and Rel Family Proteins in Living Cells Using Bimolecular Fluorescence Complementation journal April 2002
Seeing what was unseen: New analytical methods for molecular imaging journal January 2003
Circularly permuted green fluorescent proteins engineered to sense Ca2+ journal March 2001
A Fluorescent Indicator for Detecting Protein−Protein Interactions in Vivo Based on Protein Splicing journal November 2000
Antiparallel Leucine Zipper-Directed Protein Reassembly:  Application to the Green Fluorescent Protein journal June 2000
Combinatorial Marking of Cells and Organelles with Reconstituted Fluorescent Proteins journal October 2004
Protein Splicing-Based Reconstitution of Split Green Fluorescent Protein for Monitoring Protein−Protein Interactions in Bacteria:  Improved Sensitivity and Reduced Screening Time journal December 2001

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