Bradfordproteinassay

Bradford protein assay

Considerations for use

The Bradford assay is very fast and uses about the same amount of protein as the Lowry assay. It is fairly accurate and samples that are out of range can be retested within minutes. The Bradford is recommended for general use, especially for determining protein content of cell fractions and assesing protein concentrations for gel electrophoresis.

Assay materials including color reagent, protein standard, and instruction booklet are available from Bio-Rad Corporation. The method described below is for the "standard Procedure" with sensitivity to about 20 to 200 micrograms protein. Simply scale down the volume for the "microassay procedure," which uses 1 ml cuvettes. Microtiter plate protocols are also described in the flyer that comes with the kit.

Principle

The assay is based on the observation that the absorbance maximum for an acidic solution of Coomassie Brilliant Blue G-250 shifts from 465 nm to 595 nm when binding to protein occurs. Both hydrophobic and ionic interactions stabilize the anionic form of the dye, causing a visible color change. The assay is useful since the extinction coefficient of a dye-albumin complex solution is constant over a 10-fold concentration range.

Equipment

In addition to standard liquid handling supplies a visible light spectrophotometer is needed, with maximum transmission in the region of 595 nm, on the border of the visible spectrum (no special lamp or filter usually needed). Glass or polystyrene (cheap) cuvettes may be used, however the color reagent stains both. Disposable cuvettes are recommended.

Procedure

Reagents

1. Bradford reagent: Dissolve 100 mg Coomassie Brilliant Blue G-250 in 50 ml 95% ethanol, add 100 ml 85% (w/v) phosphoric acid. Dilute to 1 liter when the dye has completely dissolved, and filter through Whatman #1 paper just before use.

2. (Optional) 1 M NaOH (to be used if samples are not readily soluble in the color reagent).

The Bradford reagent should be a light brown in color. Filtration may have to be repeated to rid the reagent of blue components. The Bio-Rad concentrate is expensive, but the lots of dye used have apparently been screened for maximum effectiveness. "Homemade" reagent works quite well but is usually not as sensitive as the Bio-Rad product.

Assay

1. Warm up the spectrophotometer 15 min. before use.

2. Dilute samples with buffer to an estimated concentration of 20 to 200 micrograms/ml

3. Prepare standards containing a range of 20 to 200 micrograms protein (albumin or gamma globulin are recommended) to a standard volume (generally 1 ml or less). See how to prepare and use a protein standard curve for suggestions as to setting up the standards.

4. Prepare unknowns to estimated amounts of 20 to 200 micrograms protein per tube, same volume as the unknowns.

5. (optional) Add 0.25 ml 1 M NaOH to each sample and vortex.

6. Add 5 ml dye reagent and incubate 5 min.

7. Measure the absorbance at 590 nm.

Analysis

Prepare a standard curve of absorbance versus micrograms protein (or vice versa), and determine amounts from the curve. Determine concentrations of original samples from the amount protein, volume/sample, and dilution factor, if any. If you are unfamiliar with how to obtain a protein concentration for a diluted sample from a standard curve, see how to prepare and use a protein standard curve.

Comments

The dye reagent reacts primarily with arginine residues and less so with histidine, lysine, tyrosine, tryptophan, and phenylalanine residues. Obviously, the assay is less accurate for basic or acidic proteins. The Bradford assay is rather sensitive to bovine serum albumin, more so than "average" proteins, by about a factor of two. Immunoglogin G (IgG - gamma globulin) is the preferred protein standard. The addition of 1 M NaOH was suggested by Stoscheck (1990) to allow the solubilization of membrane proteins and reduce the protein-to-protein variation in color yield.

References

• Bradford, MM. A rapid and sensitive for the quantitation of microgram quantitites of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72: 248-254. 1976.

• Stoscheck, CM. Quantitation of Protein. Methods in Enzymology 182: 50-69 (1990)