Synchrotron SAXS data from solutions of the sensory rhodopsin II with its cognate truncated transducer in 150 mM NaCl, 25 Na/K-Pi, 1 mM EDTA, 0.05 % DDM, 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 = 0.09918 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). One solute concentration of 0.78 mg/ml was measured at 20°C. 20 successive 0.500 second frames were collected. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.
The protein of study is a non-fused complex of sensory rhodopsin II (NpSRII, UniProt ID P42196) with its cognate truncated transducer (NpHtrII(1-137), UniProt ID P42259) from Nartonomonas pharaonis. The NpSRII/NpHtrII(1-137) complex in 0.05% (w/v) n-Dodecyl β-D-maltoside (DDM) detergent forms dimers at 150 mM NaCl.
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