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Evidence for bacteriophage T7 tail extension during DNA injection
BACKGROUND: Electron micrographs of bacteriophage T7 reveal a tail shorter than needed to reach host cytoplasm during infection-initiating injection of a T7 DNA molecule through the tail and cell envelope. However, recent data indicate that internal T7 proteins are injected before the DNA molecule i...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2525648/ https://www.ncbi.nlm.nih.gov/pubmed/18710489 http://dx.doi.org/10.1186/1756-0500-1-36 |
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author | Serwer, Philip Wright, Elena T Hakala, Kevin W Weintraub, Susan T |
author_facet | Serwer, Philip Wright, Elena T Hakala, Kevin W Weintraub, Susan T |
author_sort | Serwer, Philip |
collection | PubMed |
description | BACKGROUND: Electron micrographs of bacteriophage T7 reveal a tail shorter than needed to reach host cytoplasm during infection-initiating injection of a T7 DNA molecule through the tail and cell envelope. However, recent data indicate that internal T7 proteins are injected before the DNA molecule is injected. Thus, bacteriophage/host adsorption potentially causes internal proteins to become external and lengthen the tail for DNA injection. But, the proposed adsorption-induced tail lengthening has never been visualized. FINDINGS: In the present study, electron microscopy of particles in T7 lysates reveals a needle-like capsid extension that attaches partially emptied bacteriophage T7 capsids to non-capsid vesicles and sometimes enters an attached vesicle. This extension is 40–55 nm long, 1.7–2.4× longer than the T7 tail and likely to be the proposed lengthened tail. The extension is 8–11 nm in diameter, thinner than most of the tail, with an axial hole 3–4 nm in diameter. Though the bound vesicles are not identified by microscopy, these vesicles resemble the major vesicles in T7 lysates, found to be E. coli outer membrane vesicles by non-denaturing agarose gel electrophoresis, followed by mass spectrometry. CONCLUSION: The observed lengthened tail is long enough to reach host cytoplasm during DNA injection. Its channel is wide enough to be a conduit for DNA injection and narrow enough to clamp DNA during a previously observed stalling/re-starting of injection. However, its outer diameter is too large to explain formation by passing of an intact assembly through any known capsid hole unless the hole is widened. |
format | Text |
id | pubmed-2525648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25256482008-08-27 Evidence for bacteriophage T7 tail extension during DNA injection Serwer, Philip Wright, Elena T Hakala, Kevin W Weintraub, Susan T BMC Res Notes Short Report BACKGROUND: Electron micrographs of bacteriophage T7 reveal a tail shorter than needed to reach host cytoplasm during infection-initiating injection of a T7 DNA molecule through the tail and cell envelope. However, recent data indicate that internal T7 proteins are injected before the DNA molecule is injected. Thus, bacteriophage/host adsorption potentially causes internal proteins to become external and lengthen the tail for DNA injection. But, the proposed adsorption-induced tail lengthening has never been visualized. FINDINGS: In the present study, electron microscopy of particles in T7 lysates reveals a needle-like capsid extension that attaches partially emptied bacteriophage T7 capsids to non-capsid vesicles and sometimes enters an attached vesicle. This extension is 40–55 nm long, 1.7–2.4× longer than the T7 tail and likely to be the proposed lengthened tail. The extension is 8–11 nm in diameter, thinner than most of the tail, with an axial hole 3–4 nm in diameter. Though the bound vesicles are not identified by microscopy, these vesicles resemble the major vesicles in T7 lysates, found to be E. coli outer membrane vesicles by non-denaturing agarose gel electrophoresis, followed by mass spectrometry. CONCLUSION: The observed lengthened tail is long enough to reach host cytoplasm during DNA injection. Its channel is wide enough to be a conduit for DNA injection and narrow enough to clamp DNA during a previously observed stalling/re-starting of injection. However, its outer diameter is too large to explain formation by passing of an intact assembly through any known capsid hole unless the hole is widened. BioMed Central 2008-06-26 /pmc/articles/PMC2525648/ /pubmed/18710489 http://dx.doi.org/10.1186/1756-0500-1-36 Text en Copyright © 2008 Serwer et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Report Serwer, Philip Wright, Elena T Hakala, Kevin W Weintraub, Susan T Evidence for bacteriophage T7 tail extension during DNA injection |
title | Evidence for bacteriophage T7 tail extension during DNA injection |
title_full | Evidence for bacteriophage T7 tail extension during DNA injection |
title_fullStr | Evidence for bacteriophage T7 tail extension during DNA injection |
title_full_unstemmed | Evidence for bacteriophage T7 tail extension during DNA injection |
title_short | Evidence for bacteriophage T7 tail extension during DNA injection |
title_sort | evidence for bacteriophage t7 tail extension during dna injection |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2525648/ https://www.ncbi.nlm.nih.gov/pubmed/18710489 http://dx.doi.org/10.1186/1756-0500-1-36 |
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