1 / 25

Vector Conversion Simplified

Vector Conversion Simplified. U Penn School of Dental Medicine March 15, 2005 Dolores Ciufo Technology Specialist. E. coli. Native protein expression. Mammalian. N-terminal fusion protein expression . Insect. Yeast. C-terminal fusion protein expression . Others. DESTination vectors.

juan
Download Presentation

Vector Conversion Simplified

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Vector Conversion Simplified U Penn School of Dental Medicine March 15, 2005 Dolores Ciufo Technology Specialist

  2. E. coli Native protein expression Mammalian N-terminal fusion protein expression Insect Yeast C-terminal fusion protein expression Others DESTination vectors Check www.invitrogen.com/gateway for the most up-to-date vector list

  3. DEST vector list Products The most up-to-date information

  4. DEST Vector List

  5. Vectors in the freezer program Cell-free Prokaryotic

  6. Vectors in the freezer program Insect expression

  7. Vectors in the freezer program Mammalian expression vectors

  8. Destination vectors – What if the vector with the tag you need is NOT there? Solution: vector conversion

  9. R1 R2 ccdB Cmr R2 R1 Ligation Tag Tag ccdB Cmr Tag Tag Destination Vector Promoter MCS Apr Expression Vector Apr • Cassettes available in three reading frames, ready for blunt-end ligation into the MCS of any vector • Competent cell strain available for propagating Destination plasmids: One-ShotTM Survivor ccdB Competent Cells Vector conversion Any vector can be Gateway® compatible

  10. Features of conversion cassette 3 cassettes for 3 different reading frames ~1.7 Kb blunt ended double stranded DNA attR1 and attR2 sites Chloramphenicol resistance marker ccdB gene Unique restriction enzyme site RfA MluI RfB Bgl II RfC.1 XbaI

  11. Proctocol • Choose the appropriate Rf cassette • Linearize the vector with a restriction enzyme(s). If the restriction enzyme generates an overhang, blunt the ends. • 3. Remove the 5’ phosphates using calf intestinal alkaline phosphatase (CIAP). • 4. Ligate the Rf cassette into your vector using T4 DNA ligase. • 5. Transform the ligation rxn into One Shot® ccdB Survival™ Competent E. coli and select transformants on 15-30 ug/ml chloramphenicol agar. • 6. Analyze transformants – check orientation of cassette.

  12. BsrGI BsrGI **Cannot be TG or TA BsrGI BsrGI **Cannot be GA or AA or AG BsrGI BsrGI Reading frames cassettes Rf A Rf B Rf C.1 Non-shaded region becomes part of attB site

  13. Reading frames of attR sites Reading frame Reading frame Rf A 2 1 3 1 2 3 BsrGI BsrGI Rf B **Cannot be TG or TA BsrGI BsrGI Rf C.1 **Cannot be GA or AA or AG BsrGI BsrGI

  14. Terminates after a complete codon triplet ......... RfA If the coding sequence of the blunt end... use.... Encodes 2 bases of a complete codon triplet ...... RfB Encodes 1 base of a complete codon triplet ...... RfC.1 Vectors with N-terminal fusion tags TIP: Keep the AAA-AAA triplets of the attR1 site in frame with the translation reading frame of the N-terminal fusion tag in the vector being converted

  15. If the coding sequence of the blunt end... use.... Terminates after a complete codon triplet ...... RfB Encodes 2 bases of a complete codon triplet ...... RfC.1 Encodes 1 base of a complete codon triplet ..... RfA Vectors with C-terminal fusion tags TIP: Keep the TAC-AAA triplets of the attR2 site in frame with the translation reading frame of the C-terminal fusion tag in the vector being converted

  16. Vector Conversion Examples

  17. CMV pr N-term HA Tag

  18. …………………. …………………. CMV pr N-term HA MCS showing HA tag HA tag Sfi I G GCC NNN N/NGGCC C CGG N/NNNNCCGG GC/GGCCGC NotI CGCCGG/CG Sfi I G GCC NNNN C CGG N GGCCGC NotI CG Klenow rxn Sfi I G GCC NNN N C CGG Nnn n GGCCGC NotI ccggCG

  19. Encodes 1 base of a complete codon triplet ...... RfC.1 CMV pr N-term HA MCS showing HA tag Sfi I G GCC NNN N C CGG Nnn n GG CCG C NotI cc ggC G Klenow rxn

  20. EGFP CMV pr – C-term of EGFP

  21. EGFP Kozak Age I G/ CTA G CG CTA ..........A/ CCG G TC GCC ACCATG GTG C GAT C/GC GAT ..........T GGC C/AG CGG TGG TAC CAC NheI EGFP Kozak Age I NheI G CCG GTC GCC ACCATG GTG C GAT CAG CGG TGG TAC CAC Age I NheI Gcta gCCG GTC GCC ACCATG GTG C GAT Cggc cAG CGG TGG TAC CAC EGFP Convert to Gateway C-term EGFP DEST vector Klenow Which attR site do you need to consider? Which Rf cassette should be used to keep EGFP in frame?

  22. Terminates after a complete codon triplet ...... RfB Age I NheI GCTA G CCG GTC GCC ACCATG GTG C GAT C GGC CAG CGG TGG TAC CAC EGFP Convert to Gateway C-term EGFP DEST vector TIP: Keep the TAC-AAA triplets of the attR2 site in frame with the reading frame of the C-term fusion tag Answers: attR2 RfB

  23. Do att sites impact protein expression?

  24. GUS 6xHis-Gus Trx-GUS GST-GUS MW MW MW MW 50 kDa U I U I U I U I U I U I U I U I Std GW Std GW Std GW Std GW E. coli strain BL21 U = Uninduced, I = Induced Expression in Gateway® converted vectors

  25. Questions?

More Related