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PMID: 7565735 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Correlation of two-hybrid affinity data with in vitro measurements.

Molecular and cellular biology ·Vol. 15 ·No. 10 ·1995-10-00 ·Pages 5820-9

Estojak J, Brent R, Golemis EA

Abstract

Since their introduction, the interaction trap and other two-hybrid systems have been used to study protein-protein interactions. Despite their general use, little is known about the extent to which the degree of protein interaction determined by two-hybrid approaches parallels the degree of interaction determined by biochemical techniques. In this study, we used a set of lexAop-LEU2 and lexAop-lacZ reporters to calibrate the interaction trap. For the calibration, we used two sets of proteins, the Myc-Max-Mxi1 helix-loop-helix proteins, and wild-type and dimerization-defective versions of the lambda cI repressor. Our results indicate that the strength of interaction as predicted by the two-hybrid approach generally correlates with that determined in vitro, permitting discrimination of high-, intermediate-, and low-affinity interactions, but there was no single reporter for which the amount of gene expression linearly reflected affinity measured in vitro. However, some reporters showed thresholds and only responded to stronger interactions. Finally, some interactions were subject to directionality, and their apparent strength depended on the reporter used. Taken together, our results provide a cautionary framework for interpreting affinities from two-hybrid experiments.

MeSH Terms
Bacterial Proteins/genetics Base Sequence DNA/metabolism DNA-Binding Proteins/metabolism Genes, Reporter/genetics Helix-Loop-Helix Motifs Kinetics Leucine Molecular Sequence Data Mutation Operator Regions, Genetic Protein Binding Recombinant Fusion Proteins/biosynthesis Repressor Proteins/genetics,metabolism Saccharomyces cerevisiae/genetics Serine Endopeptidases Transcriptional Activation Viral Proteins Viral Regulatory and Accessory Proteins beta-Galactosidase/genetics
Chemicals
Bacterial Proteins DNA-Binding Proteins LexA protein, Bacteria Recombinant Fusion Proteins Repressor Proteins Viral Proteins Viral Regulatory and Accessory Proteins phage repressor proteins DNA beta-Galactosidase Serine Endopeptidases Leucine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Estojak J
Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111, USA.
Brent R
Golemis E A
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1995-10-00
Pages
5820-9
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC230834
Subset
IM
Grants
NCI NIH HHS · R29 CA63366 · United States
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