Probing DNA interactions with proteins using a single-molecule toolbox: inside the cell, in a test tube, and in a computer

TL;DR

This paper reviews advanced single-molecule techniques for studying DNA-protein interactions across in vivo, in vitro, and in silico environments, providing insights into molecular dynamics and functions.

Contribution

It introduces novel experimental and computational methods for analyzing DNA-protein interactions at the single-molecule level in various settings.

Findings

Single-molecule fluorescence microscopy elucidates bacterial replisome architecture.

Computational tools extract molecular signatures from live-cell data.

Optical and magnetic tweezers enable manipulation and imaging of DNA-protein complexes.

Abstract

DNA-interacting proteins have roles multiple processes, many operating as molecular machines which undergo dynamic metastable transitions to bring about their biological function. To fully understand this molecular heterogeneity, DNA and the proteins that bind to it must ideally be interrogated at a single molecule level in their native in vivo environments, in a time-resolved manner fast to sample the molecular transitions across the free energy landscape. Progress has been made over the past decade in utilising cutting-edge tools of the physical sciences to address challenging biological questions concerning the function and modes of action of several different proteins which bind to DNA. These physiologically relevant assays are technically challenging, but can be complemented by powerful and often more tractable in vitro experiments which confer advantages of the chemical environment with enhanced detection single-to-noise of molecular signatures and transition events. Here, we discuss a range of techniques we have developed to monitor DNA-protein interactions in vivo, in vitro and in silico. These include bespoke single-molecule fluorescence microscopy techniques to elucidate the architecture and dynamics of the bacterial replisome and the structural maintenance of bacterial chromosomes, as well as new computational tools to extract single-molecule molecular signatures from live cells to monitor stoichiometry, spatial localization and mobility in living cells. We also discuss recent developments from our lab made in vitro, complementing these in vivo studies, which combine optical and magnetic tweezers to manipulate and image single molecules of DNA, with and without bound protein, in a new superresolution fluorescence microscope.