Biotin, succinimidyl ester *CAS 35013-72-0*
Biotin succinimidyl ester is the most popular amine-reactive biotin derivative for modifying proteins and other biological molecules. This primary amine coupling reagent is successfully used to selectively label Escherichia coli cell envelope proteins in vivo. It preferentially labels outer membrane, periplasmic, and inner membrane proteins as well as a specific inner membrane marker protein (Tet-LacZ).
Example protocol
PREPARATION OF STOCK SOLUTIONS
Unless otherwise noted, all unused stock solutions should be divided into single-use aliquots and stored at -20 °C after preparation. Avoid repeated freeze-thaw cycles.
1. Protein stock solution (Solution A)
Mix 100 µL of a reaction buffer (e.g., 1 M sodium carbonate solution or 1 M phosphate buffer with pH ~9.0) with 900 µL of the target protein solution (e.g. antibody, protein concentration >2 mg/mL if possible) to give 1 mL protein labeling stock solution. Note: The pH of the protein solution (Solution A) should be 8.5 ± 0.5. If the pH of the protein solution is lower than 8.0, adjust the pH to the range of 8.0-9.0 using 1 M sodium bicarbonate solution or 1 M pH 9.0 phosphate buffer. Note: The protein should be dissolved in 1X phosphate buffered saline (PBS), pH 7.2-7.4. If the protein is dissolved in Tris or glycine buffer, it must be dialyzed against 1X PBS, pH 7.2-7.4, to remove free amines or ammonium salts (such as ammonium sulfate and ammonium acetate) that are widely used for protein precipitation. Note: Impure antibodies or antibodies stabilized with bovine serum albumin (BSA) or gelatin will not be labeled well. The presence of sodium azide or thimerosal might also interfere with the conjugation reaction. Sodium azide or thimerosal can be removed by dialysis or spin column for optimal labeling results. Note: The conjugation efficiency is significantly reduced if the protein concentration is less than 2 mg/mL. For optimal labeling efficiency the final protein concentration range of 2-10 mg/mL is recommended.2. Biotin succinimidyl ester stock solution (Solution B)
Add anhydrous DMSO into the vial of Biotin succinimidyl ester to make a 10 mM stock solution. Mix well by pipetting or vortex. Note: Prepare the Biotin succinimidyl ester (Solution B) before starting the conjugation. Use promptly. Extended storage of the Biotin succinimidyl ester stock solution may reduce its activity. Solution B can be stored in freezer for two weeks when kept from light and moisture. Avoid freeze-thaw cycles.SAMPLE EXPERIMENTAL PROTOCOL
This labeling protocol was developed for the conjugate of Goat anti-mouse IgG with Biotin succinimidyl ester. You might need further optimization for your particular proteins. Note: Each protein requires distinct Biotin/protein ratio, which also depends on the properties of Biotin. Over labeling of a protein could detrimentally affects its binding affinity while the protein conjugates of low Biotin/protein ratio gives reduced sensitivity.
Run conjugation reaction
- Use 10:1 molar ratio of Solution B (Biotin)/Solution A (protein) as the starting point: Add 5 µL of the Biotin stock solution (Solution B, assuming the Biotin stock solution is 10 mM) into the vial of the protein solution (95 µL of Solution A) with effective shaking. The concentration of the protein is ~0.05 mM assuming the protein concentration is 10 mg/mL and the molecular weight of the protein is ~200KD. Note: We recommend to use 10:1 molar ratio of Solution B (Biotin)/Solution A (protein). If it is too less or too high, determine the optimal Biotin/protein ratio at 5:1, 15:1 and 20:1 respectively.
- Continue to rotate or shake the reaction mixture at room temperature for 30-60 minutes.
Purify the conjugation
The following protocol is an example of dye-protein conjugate purification by using a Sephadex G-25 column.- Prepare Sephadex G-25 column according to the manufacture instruction.
- Load the reaction mixture (From "Run conjugation reaction") to the top of the Sephadex G-25 column.
- Add PBS (pH 7.2-7.4) as soon as the sample runs just below the top resin surface.
- Add more PBS (pH 7.2-7.4) to the desired sample to complete the column purification. Combine the fractions that contain the desired Biotin-protein conjugate. Note: For immediate use, the Biotin-protein conjugate need be diluted with staining buffer, and aliquoted for multiple uses. Note: For longer term storage, Biotin-protein conjugate solution need be concentrated or freeze dried.
Calculators
Common stock solution preparation
Table 1. Volume of DMSO needed to reconstitute specific mass of Biotin, succinimidyl ester *CAS 35013-72-0* to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.
0.1 mg | 0.5 mg | 1 mg | 5 mg | 10 mg | |
1 mM | 292.929 µL | 1.465 mL | 2.929 mL | 14.646 mL | 29.293 mL |
5 mM | 58.586 µL | 292.929 µL | 585.857 µL | 2.929 mL | 5.859 mL |
10 mM | 29.293 µL | 146.464 µL | 292.929 µL | 1.465 mL | 2.929 mL |
Molarity calculator
Enter any two values (mass, volume, concentration) to calculate the third.
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Citations
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References
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Authors: Bogusiewicz A, Mock NI, Mock DM.
Journal: Anal Biochem (2005): 98
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Authors: Bogusiewicz A, Mock NI, Mock DM.
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Authors: Bogusiewicz A, Mock NI, Mock DM.
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Design, synthesis, and evaluation of 5'-S-aminoethyl-N(6)- azidobenzyl-5'-thioadenosine biotin conjugate: a bifunctional photoaffinity probe for the es nucleoside transporter
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Authors: Addo JK, Buolamwini JK.
Journal: Bioconjug Chem (2004): 536
Biotin is endogenously expressed in select regions of the rat central nervous system
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Authors: McKay BE, Molineux ML, Turner RW.
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