根拠: SAXS, Size-exclusion chromatography-coupled small-angle X-ray scattering (SEC-SAXS) was performed to assess the oligomerisation state of glycosylated (high mannose) Mossman virus receptor ...根拠: SAXS, Size-exclusion chromatography-coupled small-angle X-ray scattering (SEC-SAXS) was performed to assess the oligomerisation state of glycosylated (high mannose) Mossman virus receptor binding protein in solution. Using the dimeric crystal structure data a best fitting model was generated using molecular dynamics, which considered the flexibility of the high mannose N-linked glycans and C- and N-termini. The extensive homodimeric interface observed in the crystal structure was largely retained.