提取酵母菌总蛋白的方法

Grow 25mls yeast cells to 5x10E6.
Sequentially spin down cells in a 15 ml polypro tube.
Wash cells with 1ml ice cold ddH2O, transferrring to an eppy tube.
Recon. cells in 1 ml ice cold ddH2O containing 100ug/ml PMSF.
Add 150ul ice cold 2N NaOH + 8% 2-ME (for 1 ml 400ul 5N NaOH + 600ul ddH2O + 80ul 2-ME). Mix by inverting tube several times. Inc. on ice for 10 min.
Add 150ul ice cold 50% TCA, mix by inverting tube several times. Inc. on ice for 10 min.
Spin 2 min. in microfuge. Wash pellet with 1ml. ice cold acetone, spin 2 min. and aspirate off the supernatant. Dry pellet.
Resuspend pellet in 100 ul sample buffer: 500ul 3X Sample buffer pH6.8 + 500ul ddH2O + 12.5ul 2-ME + 25ul 1M TRIS base + 100ug PMSF + dab of bromphenol blue. You may have to work at this, I've heard a wire homogenizer does the trick.
Heat 95¡C x 2-5 min. Try loading 10ul on the gel, may need more.

Note: Make PMSF at 10mg/ml in isopropanol and stor