Purification of Bovine Brain Tubulins

Source: Banerjee, A., M. C. Roach, P. Treka, R. F. Luduena. 1990. Increased microtubule assembly in bovine brain tubulin lacking the type III isotype of β-tubulin. J. Biol. Chem. 265: 1794–1799.

Corresponding chapter(s) in the textbook: Chapter 13 (and 4)

Review the following terms before working on the problem: cytoskeleton, microtubules, tubulins, agarose, column chromatography, polyacrylamide gel electrophoresis, Coomassie Blue staining, Western blotting

Read the paper and answer the questions below that refers to the data described in Figure 1 of the paper.

Be prepared to discuss the other experiments described, in class.

Experiment

Tubulin was isolated from bovine brain, purified by phosphocellulose ion exchange chromatography, and further fractionated by affinity chromatography on an anti-2-tubulin-agarose column. (Note: Affinity chromatography is a powerful separation technique based on the specific, noncovalent interaction between two molecules; in this experiment: between β2-tubulin and its antibody. The antibody is immobilized on agarose beads, and the protein solution is passed through the antibody-agarose column. Unbound molecules are washed out with excess sample buffer, and the specifically bound proteins are eluted with a high-salt solution.)

The original tubulin (PC, for phosphocellulose-purified), the unbound fraction (U), and a bound fraction eluted from the column (B) were fractionated by polyacrylamide gel electrophoresis. The gels were subjected to the following procedures:

(a) Coomassie Blue protein staining

(b) Western blot with anti-2-tubulin

(c) Western blot with anti-1-tubulin

Figure