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Methods to Isolate Proteins from Detergent-containing Solutions for Proteome Analysis

dc.contributor.authorCrowell, Andrew
dc.contributor.copyright-releaseYesen_US
dc.contributor.degreeMaster of Scienceen_US
dc.contributor.departmentDepartment of Chemistryen_US
dc.contributor.ethics-approvalReceiveden_US
dc.contributor.external-examinern/aen_US
dc.contributor.graduate-coordinatorDr. Mark Stradiottoen_US
dc.contributor.manuscriptsYesen_US
dc.contributor.thesis-readerDr. Robert Whiteen_US
dc.contributor.thesis-readerDr. Amares Chatten_US
dc.contributor.thesis-supervisorDr. Alan Doucetteen_US
dc.date.accessioned2014-12-10T14:18:56Z
dc.date.available2014-12-10T14:18:56Z
dc.date.defence2014-12-03
dc.date.issued2014-12-10
dc.description.abstractThe use of the detergent sodium dodecyl sulfate (SDS) to assist in the solubilization of protein samples can be highly beneficial in the proteomics workflow. However, SDS is incompatible with LC-MS. Acetone precipitation is an effective means of depleting SDS from protein samples. However, inconsistent and variable yields have limited the use of this technique as a front-end purification strategy ahead of MS. This thesis provides an in-depth characterization of protein recovery through acetone precipitation. An improved protocol is proposed, using an increased amount of ionic buffer to ensure proper protein precipitation efficiency. The use of a filter cartridge to separate the organic solvent from the protein pellet is examined. High SDS removal (99.75%) efficiency and high protein recovery (>80%) were found to be possible with this device. Overall, this work provides evidence that acetone precipitation is an effective method to deplete SDS ahead of MS analysis.en_US
dc.identifier.urihttp://hdl.handle.net/10222/55988
dc.language.isoenen_US
dc.subjectBioanalyticalen_US
dc.subjectProteomicsen_US
dc.subjectMass Spectrometryen_US
dc.subjectSample Preparationen_US
dc.titleMethods to Isolate Proteins from Detergent-containing Solutions for Proteome Analysisen_US

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