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        (交流)PREDICTION OF B CELL EPITOPE (外国专家给我的信)

        丁香园论坛

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        小弟因为课题需要,要对融合蛋白进行B CELL EPITOPE 预测,一时没有办法下手。在网站上游荡许久,找到一个专门从事这项研究的专家,于是给他发信求助。他还真是好人,给我回了这封信,关于表位预测的,希望对大家有用:

        Thank you for your interest in my work. Unfortunately there is no accurate
        method for predicting Linear B cell epitopes currently available via the
        internet. Protein sequence profiling methods using Hydrophilicity, Flexibility,
        and Accessibility etc... do not work well. However if you choose to use one of
        these methods they can be found here:
        http://www.imtech.res.in/raghava/bcepred/

        If your intention is to successfully predict only 1 or 2 epitopes form your
        protein I would recommend trying to find protruding loop or turn structures
        located on the surface of the protein. If there is a known 3D structure of your
        protein in the PDB database this should be quite easy. Programs such as DSSP or
        STRIDE can analyze your 3D protein structure and tell you were these regions
        are and how accessible they are.
        Available here:
        http://bioweb.pasteur.fr/seqanal/interfaces/dssp-simple.html
        http://bioweb.pasteur.fr/seqanal/interfaces/stride.html

        If you do not have a known structure for your protein I would use a secondary
        structure prediction program such as JPRED or PREDATOR to predict the location
        of loop and turn structures within your protein

        http://www.compbio.dundee.ac.uk/~www-jpred/
        http://bioweb.pasteur.fr/seqanal/interfaces/predator-simple.html

        Once you have found a region of your protein that you think is likely to
        contain a B cell epitope I would also recommend synthesising a large peptide of
        approximately 15 amino acids to cover it as the local secondary structure maybe
        important in enabling an antibody to cross-react.

        Finally, I do not know a great deal about recombinant protein technology but I
        would imagine that so long as a predicted B cell epitope is still accessible
        and is not masked from being fussed to another protein (i.e. The predicted
        epitope is not facing the join to the other protein) the fussing or your
        protein should not have a significant effect.

        I hope I have been of some help to you,

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