Identification and characterization of new cellular interacting proteins of HIV-1 integrase

dc.contributor.authorParvez, Md. Kamal Uddin
dc.contributor.examiningcommitteeFowke, Keith (Medical Microbiology) Peng, Zhikang (Immunology) Cheng, keding (Human Anatomy & Cell Science)en
dc.contributor.supervisorYao, Xiaojian (Medical Microbiology)en
dc.date.accessioned2011-04-12T17:31:06Z
dc.date.available2011-04-12T17:31:06Z
dc.date.issued2011-04-12T17:31:06Z
dc.degree.disciplineMedical Microbiologyen_US
dc.degree.levelMaster of Science (M.Sc.)en_US
dc.description.abstractHIV-1 integrase (IN) enzyme employs several viral and cellular proteins for nuclear translocation and crucial integration of viral cDNA. Successful identification of new viral/cellular interactions may shed light for better understanding of HIV-1 replication. 293T cells were transiently transfected with pYEF-1-TAP-IN and cell lysate were subjected to Tandem Affinity Purification system to pull down putative IN-interacting cellular partners. A number of distinct bands from the Coomassie-stained gel were excised followed by in-gel digestion and mass spectrometry. Putative cellular partners of HIV-1 IN were heat shock protein 60 (HSP60), β-tubulin, γ-actin, ATP synthase alpha subunit and histone H1.2 were identified by mass spectrometry. Additionally, SF3A3 (splicing factor 3A3), another previously reported factor, was successfully co-immunoprecipitated with IN. The C-terminal portion of IN was found to be the region of interaction with SF3A3. Overall, this study has provided better understanding of IN dynamics enriching existing knowledge of HIV-1 IN biology.en
dc.description.noteMay 2011en
dc.format.extent7332987 bytes
dc.format.mimetypeapplication/pdf
dc.identifier.urihttp://hdl.handle.net/1993/4525
dc.language.isoengen_US
dc.rightsopen accessen_US
dc.subjectHIV-1en
dc.subjectIntegraseen
dc.titleIdentification and characterization of new cellular interacting proteins of HIV-1 integraseen
dc.typemaster thesisen_US
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