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. 1998 Sep 29;95(20):11709–11714. doi: 10.1073/pnas.95.20.11709

Figure 1.

Figure 1

VEGF-B binds selectively to VEGFR-1. (A) Metabolically labeled VEGF165, mVEGF-B167, mVEGF-B186, or VEGF-C was precipitated by using receptor-Ig fusion proteins bound to protein A-Sepharose, or immunoprecipitated with specific antibodies as described in the text. Approximately 50 ng of each receptor-Ig was used. The precipitates were analyzed by SDS/PAGE in reducing conditions. (B) mVEGF-B167 and mVEGF-B186 were bound to VEGFR-1-Ig as above in the absence (−) or presence (+) of 2 μg of recombinant hVEGF165. (C) Displacement of 125I-hVEGF165 from NIH 3T3/VEGFR-1 cells by mVEGF-B186 or mVEGF164. (D) Displacement of 125I-hVEGF165 from NIH 3T3/VEGFR-1 cells by conditioned medium containing equal amounts of mVEGF-BEx1–5 wild-type (WT) or mutant forms. Mean ± SD of triplicate samples in one of three independent experiment is shown.