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| Hello every body. I am a new member. My name is Minh. I come from proteomics Lab, Institute of Biotechnology, Hanoi, Viet nam. I have some difficulties in a proteomics application to identify HBs Ag (from a recombinant vaccine sample). The sample comprises: HBs Ag 20ug/ml; Al(OH)3 < 1.25mg/ml; Themerosal< 0.1<%; formaldehyde<0.01%. I tried several methods: 1. SDS-PAGE of 100ul sample (dryness), 1 observed band (Mw appro. 22kda) then was cut and followed by ingel-digestion and ESI-1DLCMS/MS identification (AB_QSTAR XL system). 2. Direct trypsin digestion (insolution digestion) of 100ul sample (dryness), following by ESI-1DLCMS/MS identification. I spent more than 2 weeks on doing this work. now, I still do not identify the protein of interest. I think that Al(OH)3 may impact on ability of trypsin digestion. But I don't know how to remove the impact. If you have experiences or any idea, please suggest me how to solve this problem. I am looking forward to hearing from you soon. Thanks and best regards. Pham Dinh Minh Protein Biochemistry Lab, Institute of Biotechnology Vietnamese Academy of Science & Technology 18 Hoang Quoc Viet Street, Cau Giay Dist., Ha Noi , Viet Nam Tel: (+84)-4-7561903 Fax: (+84)-4-8363144 Emai: minhphd@ibt.ac.vn |
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| Dear oBWhat Thank you very much for the suggestions. I tried some methods like that, such as recovery of proteins form ziptip c18, or ingel digestion. But the problem is I dont understand the bounds between proteins and AL(0H)3, and how the bounds impact on trypsin digestion and molecular weigh of peptides after digestion. Please share me your ideas. To all members in forum: If you have any ideas, please suggest me! Thanks alot! |
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