When yeast "a" and "alpha" cells encounter mating pheromones of the opposite cell type they induce genes necessary for mating, arrest the cell cycle in G1, alter cell surface and nuclear determinants, and also undergo dramatic morphological elongation into pear shapes, affectionately termed "schmooing". These alterations prepare the yeast cells for mating and fusion to form stable diploids. The a/alpha diploids are not responsive to mating pheromone of either type, but can be induced to undergo meiosis via nutrient deprivation. The use of yeast mating pheromones has pioneered the study of the cell cycle, cellular morphology, transcriptional induction, as well as signal transduction pathways. Zymo Research provides the a-factor peptide mating pheromone as a ready to use liquid that has been optimized for both activity and stability and is guaranteed to retain biological function through multiple freeze-thaw cycles.

Concentration	1 mg/ml in methanol
Molecular Weight	1630.0 Da
Product Storage	Store at -20°C. a-factor is stable during multiple freeze-thaw cycles.
Purity	> 80% by HPLC
Structure	a-Factor is a farnesylated dodecapeptide
Usage	We recommend using the a-factor at concentrations of 0.5 µg/ml (BAR1Δ). However, BAR1 strains have not been tested. To dilute the a-factor to working concentrations, we recommend using 0.5 mg/ml BSA (bovine serum albumin) in water.

Alpha-factor mating pheromone was used to arrest and synchronize yeast cells at the G1 phase while expression of CopN protein was induced. Synchronization resulted in a homogenous cell culture which was important for studying the effects CopN had on cell cycle progression.

Huang, J., et al. (2008). The essential role of the CopN protein in Chlamydia pneumonia intracellular growth. Nature, 456: 112-115