Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

How reliable are experimental protein-protein interaction data?

Einat Sprinzak1, Shmuel Sattath, Hanah Margalit

  • 1Department of Molecular Genetics and Biotechnology, Faculty of Medicine, P.O. Box 12272, The Hebrew University of Jerusalem, 91120, Jerusalem, Israel.

Journal of Molecular Biology
|March 29, 2003
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Codon bias shapes bacterial small RNA binding sites within protein-coding sequences.

RNA (New York, N.Y.)·2026
Same author

Formation of a membraneless compartment regulates bacterial virulence.

Nature communications·2025
Same author

Unraveling the interplay between a small RNA and RNase E in bacteria.

Nucleic acids research·2024
Same author

RIL-seq reveals extensive involvement of small RNAs in virulence and capsule regulation in hypervirulent Klebsiella pneumoniae.

Nucleic acids research·2024
Same author

Prolonged survival of a patient with active MDR-TB HIV co-morbidity: insights from a <i>Mycobacterium tuberculosis</i> strain with a unique genomic deletion.

Frontiers in medicine·2023
Same author

TRS: a method for determining transcript termini from RNAtag-seq sequencing data.

Nature communications·2023

Assessing protein-protein interactions is crucial for understanding cellular networks. This study estimates the reliability of yeast two-hybrid assays at 50%, revealing key insights into the yeast interactome.

Area of Science:

  • Molecular Biology
  • Systems Biology
  • Bioinformatics

Background:

  • Protein-protein interactions (PPIs) are fundamental to cellular functions, forming complex molecular networks.
  • The accuracy and reliability of experimentally determined PPI data, particularly from high-throughput methods, are often debated.
  • A robust method is needed to evaluate the quality of PPI datasets.

Purpose of the Study:

  • To develop a computational method for directly assessing the true positive rate in experimentally determined PPI datasets.
  • To rigorously evaluate the reliability of high-throughput yeast two-hybrid (Y2H) assays.
  • To estimate the size of the yeast interactome based on reliable interaction data.

Main Methods:

  • A novel computation was developed to directly assess the true positive rate within PPI datasets.

Related Experiment Videos

  • The method was applied to analyze data generated from high-throughput yeast two-hybrid assays.
  • Statistical analysis was employed to estimate the size of the yeast interactome.
  • Main Results:

    • The reliability of high-throughput yeast two-hybrid assays was determined to be approximately 50%.
    • The computation provides an intelligible means to directly assess the true positive rate in PPI data.
    • The estimated size of the yeast interactome ranges from 10,000 to 16,600 interactions.

    Conclusions:

    • High-throughput yeast two-hybrid assays possess a reliability rate of about 50%, necessitating careful data interpretation.
    • The developed computational approach offers a reliable way to evaluate the accuracy of PPI data.
    • The yeast interactome is estimated to comprise 10,000-16,600 interactions, providing a quantitative measure for future research.