Bacteriophage PR772 X-Ray Free Electron Laser and Cryo-Electron Microscopy Studies

abstract: Structural details about viruses and their components are important for understanding the many steps in a virus life-cycle, including entry into host cells, replication, assembly, and release of progeny virions. X-ray crystallography and electron microscopy, including cryo-EM, have been u...

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Other Authors: Contreras, Alice Stephanie (Author)
Format: Dissertation
Language:English
Published: 2019
Subjects:
Online Access:http://hdl.handle.net/2286/R.I.55695
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spelling ndltd-asu.edu-item-556952020-01-15T03:01:17Z Bacteriophage PR772 X-Ray Free Electron Laser and Cryo-Electron Microscopy Studies abstract: Structural details about viruses and their components are important for understanding the many steps in a virus life-cycle, including entry into host cells, replication, assembly, and release of progeny virions. X-ray crystallography and electron microscopy, including cryo-EM, have been used extensively for virus structural studies. Recent advances with cryo-EM have significantly advanced the field with near-atomic resolution structures of viruses being achievable. X-ray free-electron lasers (XFELs) are a novel, developing method to solve structures for non-crystalline single particle targets like viruses. Diffraction patterns can be collected directly from particles at room temperature. High quality, homogeneous virus preparations are critical for both cryo-EM and XFEL studies. Thus, optimization of virus growth and sample preparation are important steps in virus structural studies. The work described in this thesis focused on optimization of protocols for growth and purification of bacteriophage PR772 for XFEL and complementary cryo-EM studies. PR772 is one of several model viruses used in the single particle initiative (SPI) experiments at the SLAC National Laboratory Accelerator Laboratory Linac Coherent Light Source (LCLS). SPI is a collaborative international effort that works towards identifying and solving challenges of high-resolution single particle imaging using XFELs. Single particle diffraction snapshots were collected from PR772 particles prepared with optimized protocols. PR772 preparations were also used for cryo-EM imaging, with the goal to obtain a high-resolution structure of the virus. The optimization and characterization employed to assure samples suitable for XFEL and cryo-EM are detailed, along with data collected with both approaches. Dissertation/Thesis Contreras, Alice Stephanie (Author) Hogue, Brenda G (Advisor) Hogue, Ian B (Committee member) Williams, Dewight (Committee member) Arizona State University (Publisher) Microbiology eng 107 pages Masters Thesis Microbiology 2019 Masters Thesis http://hdl.handle.net/2286/R.I.55695 http://rightsstatements.org/vocab/InC/1.0/ 2019
collection NDLTD
language English
format Dissertation
sources NDLTD
topic Microbiology
spellingShingle Microbiology
Bacteriophage PR772 X-Ray Free Electron Laser and Cryo-Electron Microscopy Studies
description abstract: Structural details about viruses and their components are important for understanding the many steps in a virus life-cycle, including entry into host cells, replication, assembly, and release of progeny virions. X-ray crystallography and electron microscopy, including cryo-EM, have been used extensively for virus structural studies. Recent advances with cryo-EM have significantly advanced the field with near-atomic resolution structures of viruses being achievable. X-ray free-electron lasers (XFELs) are a novel, developing method to solve structures for non-crystalline single particle targets like viruses. Diffraction patterns can be collected directly from particles at room temperature. High quality, homogeneous virus preparations are critical for both cryo-EM and XFEL studies. Thus, optimization of virus growth and sample preparation are important steps in virus structural studies. The work described in this thesis focused on optimization of protocols for growth and purification of bacteriophage PR772 for XFEL and complementary cryo-EM studies. PR772 is one of several model viruses used in the single particle initiative (SPI) experiments at the SLAC National Laboratory Accelerator Laboratory Linac Coherent Light Source (LCLS). SPI is a collaborative international effort that works towards identifying and solving challenges of high-resolution single particle imaging using XFELs. Single particle diffraction snapshots were collected from PR772 particles prepared with optimized protocols. PR772 preparations were also used for cryo-EM imaging, with the goal to obtain a high-resolution structure of the virus. The optimization and characterization employed to assure samples suitable for XFEL and cryo-EM are detailed, along with data collected with both approaches. === Dissertation/Thesis === Masters Thesis Microbiology 2019
author2 Contreras, Alice Stephanie (Author)
author_facet Contreras, Alice Stephanie (Author)
title Bacteriophage PR772 X-Ray Free Electron Laser and Cryo-Electron Microscopy Studies
title_short Bacteriophage PR772 X-Ray Free Electron Laser and Cryo-Electron Microscopy Studies
title_full Bacteriophage PR772 X-Ray Free Electron Laser and Cryo-Electron Microscopy Studies
title_fullStr Bacteriophage PR772 X-Ray Free Electron Laser and Cryo-Electron Microscopy Studies
title_full_unstemmed Bacteriophage PR772 X-Ray Free Electron Laser and Cryo-Electron Microscopy Studies
title_sort bacteriophage pr772 x-ray free electron laser and cryo-electron microscopy studies
publishDate 2019
url http://hdl.handle.net/2286/R.I.55695
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