dc984, on Aug 11 2009, 09:22 PM, said:
Hi all,
I have some newbie questions regarding the stability of protein lysates.
1. As far as I know, protein inhibitors have to be added fresh to the lysis buffer because they don't store well (?). After cell lysis, I froze my protein lysates at -80C. However, I repeatedly freeze/thawed my samples to do several SDS-PAGEs. Would the inhibitors lose their inhibitory activity, resulting in enzyme activity once thawed? As I am doing western blot of phospho-proteins, I am especially worried with phosphatases knocking off my phosphate groups. Surely I don't need to add another round of protein inhibitors every time I thaw them?!
2. More generally, how should I store protein solutions? I've read that BSA solutions must be made fresh before use. Does this mean I can't store e.g. PBST+BSA or TBST+BSA (blocking buffers) solutions at room temperature? If I do make a stock, how does freeze-thaw cycles affect general protein solutions?
Thanks very much!!!!

Hi DC,
1. Yes, freeze-thaw cycles can compromise protein samples. It would be better to store your lysates as aliquots, and defrost as-needed. This way you can minimize the number of freeze-thaw cycles you subject your samples to. The proteinase inhibitors will be OK as long as they are frozen, but if you plan on refreezing leftovers, maybe adding some fresh would be a good idea. (I don't do this b/c I make aliquots in the amount I need, with the P.I.s in them. The minimal surplus gets discarded.) Just remember to note the addition somewhere, in case you need specific concentrations.
2. You can store TPBS and TTBS + BSA in the fridge. In our lab, TBS and PBS are used by lots of people, so we make up large batches, aliquot into 500 ml bottles, autoclave, and store until used. I add the BSA when I run my WBs, and keep leftover solution, if any, at 4C. I've used TTBS+ BSA a month after I made it and it worked fine.
Edited by lab rat, 12 August 2009 - 11:28 AM.