リン酸化抗体の作製
リン酸化は、細胞の状態を切り替えるための '細胞活性装置' としての役割を担います。胚の発生から細胞のアポトーシスに至るまで必要不可欠な現象です。
Cells are packed to the brim with protein, lipids, carbohydrates, nucleic acids, and others. To make sure all these substances work together to sustain life, they need to be regulated. Phosphorylation is a key way that cells toggle activity of their equipment, playing integral roles in processes spanning from embryonic development to apoptosis. But how does one create an antibody that can recognize the tiny bump that differentiates a phosphorylated state from a non-phosphorylated state?
In 1982, Paul Greengard’s laboratory discovered how to develop such an antibody for G-substrate, a protein highly expressed in the cerebellum [1]. To generate an antibody specific towards the dephosphorylated form, they used a short amino acid fragment of the protein with the dephosphorylated residue as the antigen. For the phosphorylated form, they used the whole protein since it happened to be the case that the phosphorylated region was highly immunogenic. After immunogenizing rabbits with these polypeptides, they purified them using an affinity column. The antibodies’ ability to distinguish between the phosphorylated and dephosphorylated forms was then validated using immunoprecipitation and radioimmunoassays. The most exciting part of this method is its adaptability to any phosphoprotein. In 1991, a refined version was described in a methods paper [2].
In 1992, Richard Epstein, Charles Stiles, and colleagues described an alternative, but similar method called Activation-Specific Phosphoprotein Immunodection (APHID) [3]. Two years later, Epstein and Stiles filed a patent for this method [4]. On the surface, this sounds like Epstein and Stiles have patented all production of phosphoprotein antibodies and could prevent any company from producing or selling phosphoprotein antibodies. However, the patent covers only one specific method; it covers neither the phosphoprotein antibodies themselves nor all methods of creating phosphoprotein antibodies. Although the general idea is the same as the Greengard laboratory (i.e., using a phosphorylated fragment as the antigen), APHID differs in a key detail. In the 1991 Greengard method, the synthesized polypeptide is phosphorylated using an appropriate kinase while the APHID method takes advantage of advances in chemical synthesis. Chemical methods of synthesis are more efficient and tractable than kinases. In the late 1990s, the Greengard laboratory updated the protocol further to reflect progress in chemistry and protein purification [reviewed in 5-6].
Today, phosphoprotein antibodies are made in a similar way to that described by the Greengard laboratory. Hundreds are now commercially available, providing essential tools for cancer research, development, and countless other fields.
References
- Nairn, A, Detre, J, Casnellie, J & Greengard, P. Nature 299, 734–736 (1982).
- Czernik, A, Girault, J, Nairn, A, Chen, J, Snyder, G, Kebabian, J & Greengard, P. Methods in Enzymology 201 264–283 (1991).
- Epstein, R, Druker, B, Roberts, T, & Stiles, C. Proc. Natl. Acad. Sci. 89 10435–10439 (1992).
- Epstein, R. & Stiles, C. Activation-state Specific Phosphoprotein Immunodetection. (1994).
- Czernik AJ, Mathers J, Tsou K, Greengard P, Mische SM. Phosphorylation state-specific antibodies: preparation and applications. Neuroprotocols 6 56–61 (1995).
- Czernik AJ, Mathers J, Mische. Neuromethods 30 219–250 (1997).
