I expressed protein and unfortunately it became insoluble and remained in cell pellet. How do I get protein from pellet, so later I can use it for antibodies production?
Over-expression of a heterologous protein usually rsults in the formation of insoluble inclusion bodies. This results primarily because of the overloading of protein folding machinery of host. There are different ways of getting the soluble protein fro the inclusion bodies and one of the most commonly used method is solubilizing the inclusion bodies with guanidinium hydrochloride or urea. Once the protein is solubilized the denaturant is allowed to slowly dialyse out. The refolding conditions have to be determined and optimized for the protein in question. The extent of refolding can be measured by determining the amount of refolded protein.from a given sample.
There is lot of literature available on recovery and refolding of insoluble proteins.
Hello Prem! There are a number of detergents widely used to solublize protein. I can tell u some detergents: trition, CHAPS, sarkosyl, urea. Generally, sarkosyl works well,however it is a harsh detergent and may affect your protein activity. In case you use it try to optimize and use as less as possible to get enough protein for purification.Also make sure you remove the detergent by dialysis, so that it does not hamper your further applications.
thank you everyone for your valuable suggestions. Does it possible to run insoluble pellet on SDS-PAGE, then cut out the band, elute out and followed by the renaturation process?