4.4 Review

Determination of protein-protein interactions at the single-molecule level using optical tweezers

Journal

QUARTERLY REVIEWS OF BIOPHYSICS
Volume 55, Issue -, Pages -

Publisher

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033583522000075

Keywords

Protein-protein interaction; optical tweezers; Dudko-Hummer-Szabo model; force spectroscopy; binding parameters

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Funding

  1. FONDECYT [1181361, PCI PII20150073]

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This article introduces the application of single-molecule experiments in studying biomolecular interactions, with a focus on optical tweezer experiments for applying and measuring forces in molecular systems. The use of optical trapping allows for the revelation of hidden mechanisms and interactions, and various parameters characterizing the energy landscape of the interactions can be obtained.
Biomolecular interactions are at the base of all physical processes within living organisms; the study of these interactions has led to the development of a plethora of different methods. Among these, single-molecule (in singulo) experiments have become relevant in recent years because these studies can give insight into mechanisms and interactions that are hidden for ensemble-based (in multiplo) methods. The focus of this review is on optical tweezer (OT) experiments, which can be used to apply and measure mechanical forces in molecular systems. OTs are based on optical trapping, where a laser is used to exert a force on a dielectric bead; and optically trap the bead at a controllable position in all three dimensions. Different experimental approaches have been developed to study protein-protein interactions using OTs, such as: (1) refolding and unfolding in trans interaction where one protein is tethered between the beads and the other protein is in the solution; (2) constant force in cis interaction where each protein is bound to a bead, and the tension is suddenly increased. The interaction may break after some time, giving information about the lifetime of the binding at that tension. And (3) force ramp in cis interaction where each protein is attached to a bead and a ramp force is applied until the interaction breaks. With these experiments, parameters such as kinetic constants (k(off), k(on)), affinity values (K-D), energy to the transition state Delta G(not equal), distance to the transition state Delta x(not equal) can be obtained. These parameters characterize the energy landscape of the interaction. Some parameters such as distance to the transition state can only be obtained from force spectroscopy experiments such as those described here.

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