Synchrotron SAXS data from solutions of labrum-interacting protein from saliva in 25 mM HEPES/NaOH, 0.1 M NaCl, pH 8 were collected on the BM29 beam line at the ESRF (Grenoble, France) using a Pilatus 1M detector at a sample-detector distance of 2.9 m and at a wavelength of λ = 0.099 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Size exclusion chromatography coupled to SAXS (SEC-SAXS) was carried out at at 20°C using Nexera High Pressure Liquid Chromatography system (HPLC; Shimadzu). 50 μL of LIPS-2 concentrated at 10 mg/mL were injected into a Superdex 75 3.2/300 PC (GE Healthcare), pre-equilibrated with 25 mM HEPES/NaOH, 100 mM NaCl, pH 8.0. 82 successive 1 second frames were collected through the sample elution peak and processed using CHROMIXS that included the identification and subtraction of an appropriate solvent-blank.
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