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General Scheme. Some Biotinylated Chemical Moiety. Index of DNA Dumbells. Biotin labels. Addition of Streptavidin. Origami Schematic. Method. Conjugate different functional groups to selected staple strandsBind biotin to selected staple strandsVisualize formation or cleavage of individual chemical bonds by attachment or removal of biotin-streptavidin complex12 specific staples modifiedImaged under liquid in tapping mode AFM.
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1. “Single-molecule chemical reactions on DNA origami” Niels V. Voigt, Thomas Tørring, AlexandruRotaru, Mikkel F. Jacobsen, Jens B. Ravnsbæk, RameshSubramani, WaelMamdouh, JørgenKjems, AndriyMokhir, FlemmingBesenbacher& Kurt VesteragerGothelf, Nat Nano 5, no. 3 (March 2010): 200-203.
3. Origami Schematic
4. Method Conjugate different functional groups to selected staple strands
Bind biotin to selected staple strands
Visualize formation or cleavage of individual chemical bonds by attachment or removal of biotin-streptavidin complex
12 specific staples modified
Imaged under liquid in tapping mode AFM
5. Linkers Linker A – non-cleavable linker
Linker B – disulphide bond cleaved by reduction
Applied 1,4-dithiothreitol (DTT)
Linker C – 1,2-bis(alkylthio)ethene cleaved by singlet oxygen
Applied singlet oxygen photosensitizer eosin and white light
6. Linker Images
7. Chemical Bond CleavageRxns Assembly Anneal Concentration: 5nM
1:30 viral DNA:staples
Annealed in 1 x TAE-Mg2+ (12.5mM Mg Acetate) – pH=8.0
Thermal Anneal: 90°C - 4°C over 14 hrs (0.1°C/min)
Purified using 100kDa MWCO centrifugal filter
Streptavidin (2uM) incubated for 2 hrs
8. Reductive Cleavage with DTT In solution
10mM DTT incubated with unfiltered origamis for 6 hrs at RT
Streptavidin added for 2 hrs at RT
AFM
On mica
Filtered origami added to cleaved mica (adsorbed 3 min)
Incubate with 30mM DTT 4 hrs at RT
Washed surface with 1xTAE-Mg2+
Results were comparable
9. Cleavage with singlet Oxygen On mica
Sample deposited on mica after DTT treatment
Added eosin (100uM) and DTT (1mM)
Irradiate samples with 150 W for 60 min
Remove buffer and wash 2x with 1xTAE-Mg2+
10. Single Molecule Bond Formation Alkyne
Copper(I)-catalyzed click reaction w/ azide to form triazole
Amine
Reacts w/ N-hydroxysuccinimide activates ester (NHS-ester) to form amide
Azide
Copper(I)-catalyzed click reaction w/ alkyne to form triazole
11. Single Molecule Images
12. Chemical Bond FormingRxns Assembly Anneal Concentration: 10 nM
1:10 viral DNA:staples
Annealed in 20mM HEPES buffer (12.5mM MgCl2) – pH=7.4
Thermal Anneal: 90°C - 4°C over 14 hrs (0.1°C/min)
13. SM reaction Conditions Origami deposited on Mica under HEPES/Mg2+ buffer (pH=7.4)
Alkyne
Copper(I)-THTA in DMF/buffer mixture
Amine
Slightly alkaline buffer/DMF mixture (pH=8.3)
Azide
Copper(I)-THTA catalyst
Incubate reagents for 20 min
Incubate with streptavidin for 5 min
14. First Click Rxn On mica
Origami added to cleaved mica (adsorbed 3 min)
Add HEPES/Mg2+ buffer
Image with AFM
Remove buffer and add coupling solution
Coupling soln: CuSO4 (200uM), THTA(1.4mM), Sodium ascorbate (20mM), azidefunctionalized biotin (10mM)
Incubate for 20 min
Wash with HEPES/Mg2+ buffer
Incubate with streptavidin (200nM) in HEPES/Mg2+ buffer 5 min
Wash and Image with AFM
15. Amine and Activated Acid Rxn On mica
Origami added to cleaved mica (adsorbed 3 min)
Add HEPES/Mg2+ buffer
Image with AFM
Remove buffer and add coupling solution
Coupling soln: Biotin-NHS (10mM), 1:4 DMF/Buffer (HEPES; 20mM, Mg2+; 12.5mM, pH=8.26)
Incubate for 20 min
Wash with HEPES/Mg2+ buffer
Incubate with streptavidin (200nM) in HEPES/Mg2+ buffer 5 min
Wash and Image with AFM
16. Second Click Rxn On mica
Origami added to cleaved mica (adsorbed 3 min)
Add HEPES/Mg2+ buffer
Image with AFM
Remove buffer and add coupling solution
Coupling soln: CuSO4 (200uM), THTA(1.4mM), Sodium ascorbate (20mM), alkyne functionalized biotin (5mM in DMF/HEPES/Mg2+)
Incubate for 20 min
Wash with HEPES/Mg2+ buffer
Incubate with streptavidin (200nM) in HEPES/Mg2+ buffer 5 min
Wash and Image with AFM
Note: Imaging conditions make index difficult to see
17. Yield Calculation
18. Yields