Yu Xiaoli, Gilden Donald H, Ritchie Alanna M, Burgoon Mark P, Keays Kathryne M, Owens Gregory P
Department of Neurology, University of Colorado Health Sciences Center, 4200 E. 9th Avenue, Mail Stop B182, Denver, Colorado 80262, USA.
J Neuroimmunol. 2006 Mar;172(1-2):121-31. doi: 10.1016/j.jneuroim.2005.11.010. Epub 2005 Dec 20.
We generated recombinant antibodies (rAbs) from over-represented IgG sequences expressed by single plasma cells from multiple sclerosis (MS) cerebrospinal fluid (CSF). Panning of a phage-displayed random peptide library with the rAbs revealed several specific peptide sequences. Inhibition assays confirmed specific binding of the peptides to the antigen-binding site of the antibody. The native IgG of MS CSF from which the recombinant antibody was cloned also recognized these peptides. Our data demonstrate that MS rAb reflects the specificity of IgG in the CSF. Thus, the epitopes/mimotopes identified by MS rAb may provide clues to disease-relevant antigens.
我们从多发性硬化症(MS)脑脊液(CSF)中单个浆细胞表达的高丰度IgG序列生成了重组抗体(rAbs)。用这些rAbs筛选噬菌体展示的随机肽库,发现了几个特定的肽序列。抑制试验证实了这些肽与抗体抗原结合位点的特异性结合。克隆重组抗体所用的MS CSF天然IgG也识别这些肽。我们的数据表明,MS rAb反映了CSF中IgG的特异性。因此,MS rAb鉴定出的表位/模拟表位可能为疾病相关抗原提供线索。