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. 2005 Dec;79(24):15398–15404. doi: 10.1128/JVI.79.24.15398-15404.2005

FIG. 3.

FIG. 3.

Binding activities of d(1-8)-SDF-1α (A) and d(1-10)-vMIP-II-(9-68)-SDF-1α (B) to wild-type CXCR4 and mutants. (A) The binding activity of d(1-8)-SDF-1α was reduced by Y45A, F87A, D171A, D187A, E288D, and DNX4. (B) The point mutation of Tyr45, Phe87, Asp97, Tyr121, Asp171, Asp187, Tyr219, Trp252, Tyr255, Asp262, Glu288, or Phe292 as well as the deletion of the N terminus impaired d(1-10)-vMIP-II-(9-68)-SDF-1α binding. All data are shown as the mean ± standard deviation from at least three independent experiments.