| Literature DB >> 27984731 |
Guanshi Wang1, Jesse Hauver2, Zachary Thomas3, Seth A Darst4, Alexandros Pertsinidis5.
Abstract
Many essential cellular processes, such as gene control, employ elaborate mechanisms involving the coordination of large, multi-component molecular assemblies. Few structural biology tools presently have the combined spatial-temporal resolution and molecular specificity required to capture the movement, conformational changes, and subunit association-dissociation kinetics, three fundamental elements of how such intricate molecular machines work. Here, we report a 3D single-molecule super-resolution imaging study using modulation interferometry and phase-sensitive detection that achieves <2 nm axial localization precision, well below the few-nanometer-sized individual protein components. To illustrate the capability of this technique in probing the dynamics of complex macromolecular machines, we visualize the movement of individual multi-subunit E. coli RNA polymerases through the complete transcription cycle, dissect the kinetics of the initiation-elongation transition, and determine the fate of σ70 initiation factors during promoter escape. Modulation interferometry sets the stage for single-molecule studies of several hitherto difficult-to-investigate multi-molecular transactions that underlie genome regulation.Entities:
Keywords: RNA polymerase; axial localization; holoenzyme; interferometry; nuclear pore complex; sigma factor; single-molecule; super-resolution imaging; transcription; transcription cycle
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Year: 2016 PMID: 27984731 PMCID: PMC5444671 DOI: 10.1016/j.cell.2016.11.032
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582