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  • Protein measurement using bicinchoninic acid: elimination of interfering substances.

Protein measurement using bicinchoninic acid: elimination of interfering substances.

Analytical biochemistry (1989-07-01)
R E Brown, K L Jarvis, K J Hyland
ABSTRACT

Protein quantitation based on bicinchoninic acid (BCA) is simple, sensitive, and tolerant to many detergents and substances known to interfere with the Lowry method. However, certain compounds often used during protein purification do interfere with the BCA protein assay. The response of the BCA chromophore to various interfering substances has provided insight into the mechanism of protein quantitation by BCA. Certain substances (e.g., glucose, mercaptoethanol, and dithiothreitol) elicit a strong absorbance at 562 nm when combined with the BCA working reagent. The absorbance appears to be identical to the normal response elicited by protein. Other agents (e.g., ammonium sulfate and certain ampholytes) diminish the protein-induced color development and shift the wave-length of the color response. Both types of interference can be eliminated by selectively precipitating protein with deoxycholate and trichloroacetic acid (A. Bensadoun and D. Weinstein (1976) Anal. Biochem. 70,241-250) prior to reaction with bicinchoninic acid. The modifications described here permit quick, efficient removal of many interfering substances that are commonly utilized during protein purification.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
QuantiPro BCA Assay Kit, for 0.5-30 μg/ml protein
Sigma-Aldrich
Bicinchoninic Acid Kit for Protein Determination, for 200-1000 μg/ml protein