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Epitope Mapping Using the Cell-Based 2 × Alanine Substitution Method About the Anti-mouse CXCR6 Monoclonal Antibody, Cx 6 Mab-1.

Yu IsodaTomohiro TanakaHiroyuki SuzukiTeizo AsanoTakeo YoshikawaKaishi KitamuraYuma KudoRyo EjimaKazuki OzawaMika K KanekoYukinari Kato
Published in: Monoclonal antibodies in immunodiagnosis and immunotherapy (2022)
An anti-mouse CXC chemokine receptor 6 (mCXCR6) monoclonal antibody (mAb), Cx 6 Mab-1, was developed recently. Cx 6 Mab-1 is applicable for flow cytometry, Western blotting, and enzyme-linked immunosorbent assay. The purpose of this study is to determine the binding epitope of Cx 6 Mab-1 using 2 × alanine mutated mCXCR6. Analysis of flow cytometry revealed that Cx 6 Mab-1 did not recognize S8A-A9G, L10A-Y11A, D12A-G13A, and H14A-Y15A mutants of mCXCR6. The results clearly indicate that the binding epitope of Cx 6 Mab-1 includes Ser8, Ala9, Leu10, Tyr11, Asp12, Gly13, His14, and Tyr15 of mCXCR6. The successful determination of the Cx 6 Mab-1 epitope might contribute to the pathophysiological investigation of mCXCR6.
Keyphrases
  • monoclonal antibody
  • flow cytometry
  • stem cells
  • high throughput
  • bone marrow
  • dna binding
  • molecularly imprinted
  • wild type