Exploring DNA-protein interactions on the single DNA molecule level using nanofluidic tools
Journal article, 2017

DNA-protein interactions are at the core of the cellular machinery and single molecule methods have revolutionized the possibilities to study, and our understanding of these interactions on the molecular level. Nanofluidic channels have been extensively used for studying single DNA molecules during the last twelve years and in this review, we discuss how this experimental platform has been extended to studies of DNA-protein interactions. We first present how the design of the device can be tailored for the specific DNA-protein system studied and how the channels can be passivated to avoid non-specific binding of proteins. We then focus on describing the different kinds of DNA-interacting proteins that have been studied in nanofluidic devices, including proteins that compact DNA and proteins that form filaments on DNA. Our main objective is to highlight the diverse functionalitiesof DNA-protein systems that have been characterized using nanofluidic structures and hence demonstrate the versatility of these experimental tools. We finally discuss potential future directions studies of DNA-protein complexes in nanochannels might take, including specific DNA-protein systems that are difficult to analyze with traditional techniques, devices with increased complexity, and fully integrated lab-on-a-chip devices for analysis of material extracted from (single) cells.

Devices

Filaments

Dynamics

Elongation

Switch

Compaction

Nanochannels

Conformations

Channels

Author

Karolin Frykholm

Chalmers, Biology and Biological Engineering, Chemical Biology

Lena Nyberg

Chalmers, Biology and Biological Engineering, Chemical Biology

Fredrik Westerlund

Chalmers, Biology and Biological Engineering, Chemical Biology

Integrative Biology (United Kingdom)

1757-9694 (ISSN) 1757-9708 (eISSN)

Vol. 9 8 650-661

Subject Categories

Biochemistry and Molecular Biology

Chemical Engineering

DOI

10.1039/c7ib00085e

More information

Created

10/7/2017