Figure 1 T-cell receptor 2D1 recognizes human leukocyte antigen (HLA)–A2–restricted octameric and nonameric synthetic peptides T-cell receptor 2D1 recognizes.

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Figure 1 T-cell receptor 2D1 recognizes human leukocyte antigen (HLA)–A2–restricted octameric and nonameric synthetic peptides T-cell receptor 2D1 recognizes human leukocyte antigen (HLA)–A2–restricted octameric and nonameric synthetic peptides Left: Fluorescence microscope images from coculture of 58α−β− T hybridoma cells expressing TCR 2D1, human CD8αβ molecules, and sGFP under the control of nuclear factor of activated T cells (58-2D1-CD8-sGFP) and COS-7 cells expressing HLA-A*02:01(COS-7-A2) cells preincubated with synthetic peptides. Green cells indicate activation of 58-2D1-CD8-sGFP cells. The names of the peptides are given as inserts. Scale bars: 100 μm. Right: Secreted interleukin (IL)–2 as measured by ELISA of the coculture's supernatants. In the top row (A–D), octameric peptides were used. Only glycerolphosphatidylcholine phosphodiesterase 1 (GPCPD1) (15-22) weakly activated 58-2D1-CD8-sGFP cells. In the second row (E–H), the same octameric peptides were used but all carried an additional methionine residue at their N-terminus. All of them strongly activated 58-2D1-CD8-sGFP cells. In the third row (I–L), the same octameric peptides were used but all carried their original amino acid residue at their N-terminus. Only GPCPD1(14-22) activated 58-2D1-CD8-sGFP cells. Lowest row: (M) The entire domain of GPCPD1(1-118) that harbors the antigenic peptide GPCPD1(14-22) did not activate 58-2D1-CD8-sGFP cells when transfected into COS-7-A2 cells. When no peptide (N) or the irrelevant peptide T-lymphotrophic virus-2 protein (TAX) (11-19) (O) was added, 58-2D1-CD8-sGFP cells were not activated. Error bars represent standard deviation of the mean. DMXL2 = Dmx-like-2; EML5 = echinoderm microtubule associated protein-like 5; NCAN = Neurocan. Geraldine Rühl et al. Neurol Neuroimmunol Neuroinflamm 2016;3:e241 © 2016 American Academy of Neurology