Protocol: Click-Chemistry Labeling of Oligonucleotides and DNA

Click chemistry is a versatile reaction that can be used for the synthesis of a variety of conjugates. Virtually any biomolecule can be easily labelled with small molecules, such as fluorescent dyes, biotin, etc using click chemistry method.

Click chemistry reaction takes place between two components: azide and alkyne (terminal acetylene). Both azido and alkyne groups are nearly never encountered in natural biomolecules. Hence, the reaction is highly bioorthogonal and specific. If there is a need to label an oligonucleotide, alkyne-modified oligonucleotides can be ordered at many of the custom oligo-synthesizing facilities and companies.

We recommend using the following general protocol for Click chemistry labeling of alkyne-modified oligonucleotides with azides produced by Lumiprobe Corp. The auxiliary reagents can be ordered at Lumiprobe Corp..

1. Calculate the volumes of reagents required for Click chemistry labeling using the table below. Prepare the required stock solutions (see Appendix).

   Reagent	Final concentration in the mixture	Stock solution concentration
   Oligonucleotide, alkyne-modified	Varies (20 – 200 uM)	varies
   Azide	1.5 x (oligonucleotide concentration)	10 mM in DMSO
   DMSO	50 vol %	-
   Ascorbic acid	0.5 mM	5 mM in water
   Cu-TBTA complex	0.5 mM	10 mM in 55 vol % DMSO

2. Dissolve alkyne-modified oligonucleotide or DNA in water in a pressure-tight vial.
3. Add 2M triethylammonium acetate buffer, pH 7.0, to final concentration 0.2 M.
4. Add DMSO, and vortex.
5. Add azide stock solution (10 mM in DMSO), and vortex.
6. Add the required volume of 5mM Ascorbic Acid Stock solution to the mixture, and vortex briefly.
7. Degass the solution by bubbling inert gas in it for 30 seconds. Nitrogen, argon, or helium can be used.
8. Add the required amount of 10 mM Copper (II)-TBTA Stock in 55% DMSO to the mixture. Flush the vial with inert gas and close the cap.
9. Vortex the mixture thoroughly. If significant precipitation of azide is observed, heat the vial for 3 minutes at 80°C, and vortex.
10. Keep at room temperature overnight.
11. Precipitate the conjugate with acetone (for oligonucleotides) or with ethanol (for DNA). Add at least 4-fold volume of acetone to the mixture (If the volume of the mixture is large, split in several vials). Mix thoroughly and keep at -20°C for 20 minutes.
12. Centrifuge at 10000 rpm for 10 minutes.
13. Discard the supernatant.
14. Wash the pellet with acetone (1 mL), centrifuge at 10000 rpm for 10 minutes.
15. Discard the supernatant, dry the pellet, and purify the conjugate by RP-HPLC or PAGE.

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