Description: This simple NHS ester is applicable for the introduction of dibenzylcyclooctyne into organic/inorganic compounds and for the modification of surfaces and particles bearing a terminal amino functionality. Once the molecule is DBCO-labeled, it can react with an azide-labeled molecule to produce a stable conjugate (triazole) via Cu(I)-free or strain-promoted click reaction. Because DBCOs and azides are absent from biological systems, there is minimal background labeling of cells or lysates.
Important Product Information
NHS esters are moisture-sensitive. To avoid moisture condensation onto the product always let the vial come to room temperature before opening, be careful to limit exposure to moisture and restore under an inert atmosphere. The NHS-ester moiety readily hydrolyzes and becomes non-reactive, therefore, prepare stock solutions immediately before use. Stock solutions in anhydrous solvents can be kept for several days (freeze when not in use).
Hydrolysis of the NHS ester is a competing reaction. Conjugation with primary amines of proteins/peptides (i.e. acylation) is favored at near neutral pH (6 - 9) and with concentrated protein solutions. For conjugation, use non-amine-containing buffers at pH 7 - 9 such as PBS (20 mM sodium phosphate, 150 mM sodium chloride, pH 7.4), 20 mM HEPES, 100 mM carbonate/biocarbonate, or 50 mM borate buffer.
Do not use buffers that contain primary amines (e.g. Tris, Glycine).
Avoid buffers that contain azides, which can react with DBCO.
Dissolve DBCO-NHS ester in a dry water-miscible organic solvent such as DMSO or DMF before diluting in final reaction buffer. DBCO-NHS ester is not soluble in aqueous buffers.
DBCO-NHS ester is a moderately hydrophobic molecule with limited solubility in aqueous buffers. We generally do not recommend using this product for labeling of biopolymers. For labeling of proteins in aqueous buffers we recommend using more hydrophilic DBCO-PEG4-NHS ester (CLK-A134) or water soluble DBCO-sulfo-NHS ester (CLK-A124).
Additional Material Required
Water-miscible organic solvent such as dimethyl sulfoxide (DMSO) or dimethyl formamide (DMF)
Reaction buffer: Phosphate-buffered saline (PBS) or other buffer at pH 5 - 9
Quenching buffer: 1 M Tris-HCl, pH 8.0
Spin Desalting Columns or Slide-A-Lyzer Dialysis Cassettes (Pierce Biotechnology)
Prepare protein in PBS.
Immediately before use, prepare 10 mM of the DBCO-NHS reagent in DMSO or DMF.
Add the NHS reagent to the protein sample at a final concentration of 0.5 - 2 mM. If the protein concentration is 5 mg/ml, use a 10 - fold molar excess of the reagent. For samples < 5 mg/ml, use a 20 - to 50 - fold molar excess.
Incubate the reaction at room temperature for 30 minutes or on ice for 2 hours.
Stop the reaction by adding Quenching Buffer to a final concentration of 50 - 100 mM Tris.
Incubate the reaction at room temperature for 5 minutes or on ice for 15 minutes.
Remove non-reactive reagent by dialysis or desalting
Long-term aqueous Stability of DBCO-labeled Samples
DBCO modified goat IgG (DOL 7) losses about 3 - 5 % of its reactivity toward azides over 4 weeks at 4 °C or -20 °C. For long time storage azide- and thiol-containing buffers should be avoided.
Direct Measurement of DBCO Incorporation
The degree of DBCO incorporation (i.e. the number of DBCO per protein molecule) can be determined from the absorbance scan of the purified conjugate (235 - 400 nm).
Copper-free Click Reaction
Prepare the azide-containing sample in reaction buffer.
Add DBCO-protein conjugate to azide-containing sample.
Recommendation: Add 1 mol equivalent of limiting protein to 1.5 - 3.0 mol equivalents of highest abundance protein.
Incubate the reaction at room temperature for 1 - 4 hours or at 4 °C for 2 - 12 hours.
The reaction is now ready for purification.
Problem: No conjugation of DBCO with azide
Possible reason: One or more sample is not labeled
- Confirm molecules were labeled or repeat activation process
Possible reason: NHS-ester hydrolyzed
- Allow product to equilibrate to room temperature before opening
- Prepare new solutions in the indicated dry solvents
- Avoid buffers that contain primary amines such as Tris and glycine
Possible reason: Excess reagent not quenched or removed
- Remove excess reagent by dialysis or desalting
Problem: Low conjugation of DBCO and azide
Possible reason: Suboptimal reaction conditions
- Increase incubation time
- Optimize conjugation conditions by altering molar excess
- Perform conjugation reactions at 37 °C
Product Citations: Please click the black arrow on the right to expand the citation list. Click publication title for the full text.
Simon et al. (2012) Facile Double-Functionalization of Designed Ankyrin Repeat Proteins using Click and Thiol Chemistries. Bioconjugate Chem.23 (2):279.
Zeng et al. (2012). 64Cu Core-Labeled Nanoparticles with High Specific Activity via Metal-Free Click Chemistry. ACS Nano.6 (6):5209.
Arumugam et al. (2011). [18F]Azadibenzocyclooctyne ([18F]ADIBO): A biocompatible radioactive labeling synthon for peptides using catalyst free [3+2] cycloaddition. Bioorg. Med. Chem. Lett.21:6987.
Campbell-Verduyn et al. (2011). Strain-Promoted Copper-Free Click Chemistry for 18F Radiolabeling of Bombesin. Angew. Chem. Int. Ed.50:11117.
Debets et al. (2010) Aza-dibenzocyclooctynes for fast and efficient enzyme PEGylation via copper-free (3+2) cycloaddition. Chem. Commun.46:97.