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Please use this identifier to cite or link to this item: http://arks.princeton.edu/ark:/88435/dsp01qz20sw62h
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dc.contributor.advisorYan, Nieng-
dc.contributor.authorKim, Minyoung-
dc.date.accessioned2021-08-20T17:53:19Z-
dc.date.available2021-08-20T17:53:19Z-
dc.date.created2021-04-16-
dc.date.issued2021-08-20-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/dsp01qz20sw62h-
dc.description.abstractThe throughput of electron cryo-microscopy (cryo-EM) can be improved by collecting data using beam-image shift instead of the traditional stage-shift method. Despite successful implementation of beam-image shift on various cryo-EM instruments, it remains unknown how beam-image shift affects the quality of data collected on spherical aberration (Cs)-corrected cryo-EM instruments. To investigate this, a cryo-EM dataset for Thermoplasma acidophilum 20S (T20S) proteasome was collected on a 300 kV Cs-corrected transmission electron microscope (TEM) using beam-image shift. Analyzing the dataset in two different image-processing software, RELION and CryoSPARC demonstrated that there are minimal differences between the resolutions of T20S structures generated from datasets collected using with and without beam-image shift. In addition, findings of this study demonstrated that data collected using with and without beam-image shift can be combined and processed together to correct for image abberations.en_US
dc.format.mimetypeapplication/pdf
dc.language.isoenen_US
dc.titleBEAM IMAGE-SHIFT ACCELERATED DATA ACQUISITION FOR SINGLE-PARTICLE ELECTRON CRYO-MICROSCOPY WITH SPHERICAL ABERRATION CORRECTIONen_US
dc.typePrinceton University Senior Theses
pu.date.classyear2021en_US
pu.departmentMolecular Biologyen_US
pu.pdf.coverpageSeniorThesisCoverPage
pu.contributor.authorid920191731
pu.mudd.walkinNoen_US
Appears in Collections:Molecular Biology, 1954-2023

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