mutagenesis and overexpression of dnase for single molecule studies

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Mutagenesis and Overexpression of DNase for Single Molecule Studies. Denise Der IM-SURE Program 2007 Mentor: Professor Philip Collins Collaborator: Professor Gregory Weiss Graduate Students: John Coroneus, Issa Moody, Jorge Lamboy. Background. - PowerPoint PPT Presentation

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  • Mutagenesis and Overexpression of DNase for Single Molecule StudiesDenise DerIM-SURE Program 2007Mentor: Professor Philip CollinsCollaborator: Professor Gregory WeissGraduate Students: John Coroneus, Issa Moody, Jorge Lamboy

  • BackgroundSingle molecule streptavidin attached to carbon nanotubeAttachment was nonspecificEDC/NHS functionalized carbon nanotubeTetrameric streptavidinFour lysines per monomer

    Figure from http://chem.ps.uci.edu/~gweiss/research.htmEDC = N-ethyl-N-(3-dimethyl aminopropyl) carbodiimide NHS = N-hydroxysuccinimide

  • GoalSite-specific protein attachment via cysteine-maleimide chemistry

    Significance: To monitor proteins in real-time, to elucidate kinetic information such as the turnover rate, and to see if the positioning of the attachment affects the performance of nano biosensor

  • BackgroundDNase domain of colicin E9Previously studiedMonomerNo cysteine residues

    Figure from the protein data bank online

  • Methodology OverviewMutagenesisOverexpressionPurificationActivity AssayAttachmentBiosensorDetector

  • Site-Specific MutationsTwo internal mutations: replacing a serine with a cysteineTwo external mutations: inserting a cysteine at the N-terminus or C-terminus

  • Quikchange

  • Verification500bp---900bp---Lane 1: 100 bp ladderLanes 2-3: colony PCR of C-30 mutantLanes 4-5: miniprep DNALanes 6-7: colony PCR of C-30 mutantLanes 8-13: colony PCR of C-49 mutant1 2 3 4 5 6 7 8 9 10 11 12 13

  • OverexpressionLane 1: molecular weight ladderLane 2: post-lysis cell pelletLane 3: post-lysis supernatantLane 4: pre-lysis supernatant

  • Flowthrough Wash Elution 1 Elution 2

  • Sample Protein GelFlowthrough Wash Elution1 of C30S mutant

  • After Dialysis against WaterLane 1: 1 kb ladderLane 2: miniprep DNALane 3: miniprep DNA + DNase

  • Arising ProblemSize exclusion chromatograph

  • Mass SpectrumExpected kDa: 15.11 kDaActual kDa: 15.104 kDa

    Impurity at 11.278 kDa

  • Future WorkTo continue working on purifying the DNase mutantsAdding protease inhibitor and inducing for less timeTo attach to a functionalized nanotubeTo measure the conductance of single molecule

  • AcknowledgementsCollins Group Members: Brett GoldsmithSteve HuntAlex KaneBucky KhalapTatyana ShepsDanny Wan Phil HaralsonYu-Jin ChenJohn CoroneusWeiss Group Members: John CoroneusIssa MoodyJorge LamboyMichael TodhunterCalvin KongSarah KiehnaLucie LeeSudipta MajumdarAgi Hajduczki Ryan Lin Cathie OverstreetJuan Diaz Glenn Eldridge IM-SURE/UROP programNational Science FoundationSaid ShokairProfessor Philip CollinsProfessor Gregory Weiss

  • Questions?

    Colors too dark?Add in a another little cartoon key here on the sidePut in protein gelDoubly charged ion