Hi Manjula,
I will lyse the bacterials cells and monitor the degradation of the lysed
protein in lysis buffer over 4-5 days before proceeding with purification.
What is the lifetime of this expressed protein once lysed? How long can it
stay after lysis without degradation or aggregation?
Does this protein contain disulfide bonds? How many? How big is this protein?
Smita Smita Mohanty, Ph.D. Associate Professor Department of Chemistry447
Physical SciencesOklahoma State UniversityStillwater, OK 74078-3071 Phone:
(405) 744 6636E-mail: Smita.Mohanty@okstate.eduWeb:
chemistry.okstate.edu/mohanty
On Monday, May 18, 2015 11:49 PM, Manjula Ramu <manjula....@gmail.com>
wrote:
Hi all,I am purifying a basic protein with pI 7.8. I used 50mM tris 8.8, 300
mm NaCl, 5% glycerol, 0.1mM PMSFand 5mM beta ME in the buffer and performed
affinity purification. Eluted with 200mM imidazole. While elution I could see
slight turbid in eluted protein (I get pure protein, single band on SDS-PAGE).
However, when I centrifuged I couldn't see any pellet. After some time(a day)
protein got degraded. In other method I tried cation exchange purification of
lysate with MES buffer pH 6.5. Here also I saw slight precipitation and later
degradation.After this again I tried with MES buffer pH 5.5 and PIPES buffer pH
6.0, here also same problem I faced.Please suggest me a method where I can get
stable protein.
Thanks and Regards,Manjula R
Research Scholar
Department of Biophysics
National Institute of Mental Health and Neurosciences
Bengaluru-29, Karnataka
INDIA
E-mail: manjula.iob@gmail.comMobile no:+91-9538553356
http://www.nimhans.kar.nic.in/
