SEC-SAXS data of Fc-hel8-L1-3

Adriana Badarau.

SASDZ46 – Engineered LysM-CHAP derivative of autolysin LytN (Fc-hel8-L1-3)

Fc-hel8-L1-3
MWexperimental 120 kDa
MWexpected 109 kDa
log I(s) 3.65×103 3.65×102 3.65×101 3.65×100
Fc-hel8-L1-3 small angle scattering data  s, nm-1
ln I(s)
Fc-hel8-L1-3 Guinier plot ln 3.65×103 Rg: 6.4 nm 0 (6.4 nm)-2 s2
(sRg)2I(s)/I(0)
Fc-hel8-L1-3 Kratky plot 1.104 0 3 sRg
p(r)
Fc-hel8-L1-3 pair distance distribution function Rg: 7.2 nm 0 Dmax: 30 nm

Data validation


There are no models related to this curve.

Synchrotron SAXS data from solutions of Engineered LysM-CHAP derivative of autolysin LytN (Fc-hel8-L1-3) in 20 mM HEPES, 150 mM NaCl, pH 7.0, pH 7 were collected on the EMBL P12 beam line at the PETRA III storage ring (DESY; Hamburg, Germany) using a Pilatus 6M detector at a sample-detector distance of 3 m and at a wavelength of λ = 0.124 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 25.00 μl sample at 5 mg/ml was injected at a 0.35 ml/min flow rate onto a Cytiva Superdex 200 Increase 5/150 column at 25°C. 1800 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.

Fc-hel8-L1-3 (Fc-hel8-L1-3)
Mol. type   Protein
Organism   S.aureus
Olig. state   Dimer
Mon. MW   54.4 kDa
Sequence   FASTA