Microfluidic approaches for the analysis of protein-protein interactions in solution.

Approaches Diffusional sizing Droplet Electrophoresis Microfluidic Protein–protein interactions

Journal

Biophysical reviews
ISSN: 1867-2450
Titre abrégé: Biophys Rev
Pays: Germany
ID NLM: 101498573

Informations de publication

Date de publication:
Apr 2020
Historique:
received: 08 01 2020
accepted: 02 03 2020
pubmed: 9 4 2020
medline: 9 4 2020
entrez: 9 4 2020
Statut: ppublish

Résumé

Exploration and characterisation of the human proteome is a key objective enabling a heightened understanding of biological function, malfunction and pharmaceutical design. Since proteins typically exhibit their behaviour by binding to other proteins, the challenge of probing protein-protein interactions has been the focus of new and improved experimental approaches. Here, we review recently developed microfluidic techniques for the study and quantification of protein-protein interactions. We focus on methodologies that utilise the inherent strength of microfluidics for the control of mass transport on the micron scale, to facilitate surface and membrane-free interrogation and quantification of interacting proteins. Thus, the microfluidic tools described here provide the capability to yield insights on protein-protein interactions under physiological conditions. We first discuss the defining principles of microfluidics, and methods for the analysis of protein-protein interactions that utilise the diffusion-controlled mixing characteristic of fluids at the microscale. We then describe techniques that employ electrophoretic forces to manipulate and fractionate interacting protein systems for their biophysical characterisation, before discussing strategies that use microdroplet compartmentalisation for the analysis of protein interactions. We conclude by highlighting future directions for the field, such as the integration of microfluidic experiments into high-throughput workflows for the investigation of protein interaction networks.

Identifiants

pubmed: 32266673
doi: 10.1007/s12551-020-00679-4
pii: 10.1007/s12551-020-00679-4
pmc: PMC7242286
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

575-585

Subventions

Organisme : Engineering and Physical Sciences Research Council
ID : EP/L015978/1
Organisme : Frances and Augustus Newman Foundation
ID : /
Organisme : Horizon 2020 Framework Programme
ID : 841466
Organisme : European Research Council
ID : FP7/2007-2013
Pays : International

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Auteurs

William E Arter (WE)

Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
Cavendish Laboratory, University of Cambridge, JJ Thomson Avenue, Cambridge, CB3 0HE, UK.

Aviad Levin (A)

Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.

Georg Krainer (G)

Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.

Tuomas P J Knowles (TPJ)

Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK. tpjk2@cam.ac.uk.
Cavendish Laboratory, University of Cambridge, JJ Thomson Avenue, Cambridge, CB3 0HE, UK. tpjk2@cam.ac.uk.

Classifications MeSH