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Three-step channel conformational changes common to DNA packaging motors of bacterial viruses T3, T4, SPP1, and Phi29. | LitMetric

Three-step channel conformational changes common to DNA packaging motors of bacterial viruses T3, T4, SPP1, and Phi29.

Virology

Division of Pharmaceutics and Pharmaceutical Chemistry, College of Pharmacy, Department of Physiology & Cell Biology, College of Medicine, and Dorothy M. Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH, USA; College of Pharmacy, Nanobiotechnology Center, Markey Cancer Center, University of Kentucky, Lexington, KY, USA. Electronic address:

Published: January 2017

AI Article Synopsis

  • - The DNA packaging motor in dsDNA bacterial viruses features a head-tail connector that allows the genome to enter during assembly and exit during infection.
  • - Recent findings regarding the phi29 virus show it uses a "One-way revolving" mechanism, which raises questions about how DNA can be ejected if the channel only allows inward movement.
  • - New research indicates that bacterial viruses (T3, T4, SPP1, and phi29) go through a three-step conformational change in their portal channels, facilitating the transition needed for DNA ejection after it has entered.

Article Abstract

The DNA packaging motor of dsDNA bacterial viruses contains a head-tail connector with a channel for the genome to enter during assembly and to exit during host infection. The DNA packaging motor of bacterial virus phi29 was recently reported to use the "One-way revolving" mechanism for DNA packaging. This raises a question of how dsDNA is ejected during infection if the channel acts as a one-way inward valve. Here we report a three step conformational change of the portal channel that is common among DNA translocation motors of bacterial viruses T3, T4, SPP1, and phi29. The channels of these motors exercise three discrete steps of gating, as revealed by electrophysiological assays. The data suggest that the three step channel conformational changes occur during DNA entry process, resulting in a structural transition in preparation for DNA movement in the reverse direction during ejection.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5107171PMC
http://dx.doi.org/10.1016/j.virol.2016.04.015DOI Listing

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