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Protein-Protein Interactions

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Cover of 'Protein-Protein Interactions'

Table of Contents

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    Book Overview
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    Chapter 1 Structural Basis of Protein-Protein Interactions
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    Chapter 2 Quantitative Analysis of Protein-Protein Interactions
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    Chapter 3 Protein-Protein Interaction Databases
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    Chapter 4 Computational Prediction of Protein-Protein Interactions
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    Chapter 5 Structure-Based Computational Approaches for Small-Molecule Modulation of Protein-Protein Interactions
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    Chapter 6 Targeting Protein-Protein Interactions for Drug Discovery
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    Chapter 7 Studying Protein-Protein Interactions Using Surface Plasmon Resonance
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    Chapter 8 Resonant Waveguide Grating for Monitoring Biomolecular Interactions
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    Chapter 9 Quartz Microbalance Technology for Probing Biomolecular Interactions
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    Chapter 10 Label-Free Kinetic Analysis of an Antibody–Antigen Interaction Using Biolayer Interferometry
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    Chapter 11 Characterization of protein-protein interactions by isothermal titration calorimetry.
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    Chapter 12 Sedimentation Equilibrium Studies
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    Chapter 13 Detecting Protein-Protein Interactions by Gel Filtration Chromatography
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    Chapter 14 Using Light Scattering to Determine the Stoichiometry of Protein Complexes
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    Chapter 15 Circular Dichroism (CD) Analyses of Protein-Protein Interactions
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    Chapter 16 Protein-Protein Interaction Analysis by Nuclear Magnetic Resonance Spectroscopy
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    Chapter 17 Quantitative protein analysis by mass spectrometry.
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    Chapter 18 Using Peptide Arrays Created by the SPOT Method for Defining Protein-Protein Interactions
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    Chapter 19 Fluorescence Polarization Assay to Quantify Protein-Protein Interactions: An Update
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    Chapter 20 Förster Resonance Energy Transfer (FRET) Microscopy for Monitoring Biomolecular Interactions.
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    Chapter 21 Utilizing ELISA to Monitor Protein-Protein Interaction
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    Chapter 22 Glutathione- S -Transferase (GST)-Fusion Based Assays for Studying Protein-Protein Interactions
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    Chapter 23 Hexahistidine (6xHis) Fusion-Based Assays for Protein-Protein Interactions
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    Chapter 24 Studying Protein-Protein Interactions via Blot Overlay/Far Western Blot
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    Chapter 25 Co-immunoprecipitation from Transfected Cells
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    Chapter 26 In Vivo Protein Cross-Linking
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    Chapter 27 Identification of protein-protein interactions by standard gal4p-based yeast two-hybrid screening.
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    Chapter 28 Reverse Two-Hybrid Techniques in the Yeast Saccharomyces cerevisiae.
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    Chapter 29 MAPPIT, a Mammalian Two-Hybrid Method for In-Cell Detection of Protein-Protein Interactions
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    Chapter 30 Bioluminescence Resonance Energy Transfer to Detect Protein-Protein Interactions in Live Cells
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    Chapter 31 Mapping Biochemical Networks with Protein Fragment Complementation Assays
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    Chapter 32 Detection of Protein-Protein Interaction Using Bimolecular Fluorescence Complementation Assay
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    Chapter 33 Split-Luciferase Complementation Assay to Detect Channel–Protein Interactions in Live Cells
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    Chapter 34 Confocal Microscopy for Intracellular Co-localization of Proteins
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    Chapter 35 Fluorescence Polarization Assay to Quantify Protein-Protein Interactions in an HTS Format
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    Chapter 36 Estrogen Receptor Alpha/Co-activator Interaction Assay: TR-FRET
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    Chapter 37 High Content Screening Biosensor Assay to Identify Disruptors of p53–hDM2 Protein-Protein Interactions
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    Chapter 38 Case Study: Discovery of Inhibitors of the MDM2–p53 Protein-Protein Interaction
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    Chapter 39 Biophysical methods for identifying fragment-based inhibitors of protein-protein interactions.
Attention for Chapter 31: Mapping Biochemical Networks with Protein Fragment Complementation Assays
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Chapter title
Mapping Biochemical Networks with Protein Fragment Complementation Assays
Chapter number 31
Book title
Protein-Protein Interactions
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2425-7_31
Pubmed ID
Book ISBNs
978-1-4939-2424-0, 978-1-4939-2425-7
Authors

Ingrid Remy, Stephen W. Michnick, Remy, Ingrid, Michnick, Stephen W.

Abstract

Cellular biochemical machineries, what we call pathways, consist of dynamically assembling and disassembling macromolecular complexes. Although our models for the organization of biochemical machines are derived largely from in vitro experiments, do they reflect their organization in intact, living cells? We have developed a general experimental strategy that addresses this question by allowing the quantitative probing of molecular interactions in intact, living cells. The experimental strategy is based on Protein fragment Complementation Assays (PCA), a method whereby protein interactions are coupled to refolding of enzymes from cognate fragments where reconstitution of enzyme activity acts as the detector of a protein interaction. A biochemical machine or pathway is defined by grouping interacting proteins into those that are perturbed in the same way by common factors (hormones, metabolites, enzyme inhibitors, etc.). In this chapter we review some of the essential principles of PCA and provide details and protocols for applications of PCA, particularly in mammalian cells, based on three PCA reporters, dihydrofolate reductase, green fluorescent protein, and β-lactamase.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 43 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Canada 2 5%
Germany 1 2%
Unknown 40 93%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 11 26%
Professor > Associate Professor 6 14%
Researcher 5 12%
Professor 5 12%
Other 4 9%
Other 7 16%
Unknown 5 12%
Readers by discipline Count As %
Agricultural and Biological Sciences 18 42%
Biochemistry, Genetics and Molecular Biology 8 19%
Medicine and Dentistry 3 7%
Pharmacology, Toxicology and Pharmaceutical Science 2 5%
Physics and Astronomy 2 5%
Other 3 7%
Unknown 7 16%