Inline small‐angle X‐ray scattering‐coupled chromatography under extreme hydrostatic pressure

Miller R, Cummings C, Huang Q, Ando N, Gillilan R, Protein Science 31(12) (2022) DOI

SASDPB7 – Acidic leucine-rich nuclear phosphoprotein 32 family member A (pp32) at 4 °C and 100 MPa (1000 atm)

Acidic leucine-rich nuclear phosphoprotein 32 family member A (L60A mutant)
MWexperimental 17 kDa
MWexpected 29 kDa
VPorod 37 nm3
log I(s) 1.46×10-3 1.46×10-4 1.46×10-5 1.46×10-6
Acidic leucine-rich nuclear phosphoprotein 32 family member A (L60A mutant) small angle scattering data  s, nm-1
ln I(s)
Acidic leucine-rich nuclear phosphoprotein 32 family member A (L60A mutant) Guinier plot ln 1.46×10-3 Rg: 2.0 nm 0 (2.0 nm)-2 s2
(sRg)2I(s)/I(0)
Acidic leucine-rich nuclear phosphoprotein 32 family member A (L60A mutant) Kratky plot 1.104 0 3 sRg
Dmax: 7.5 nm

Data validation


There are no models related to this curve.

Synchrotron SAXS data from solutions of pp32 in 25 mM BisTRIS, 10 mM NaCl, 5 mM DTT, pH 6.8 were collected on the ID7A1 BioSAXS / HP-Bio Beamline beam line at the Cornell High Energy Synchrotron Source (CHESS; Ithaca, NY, USA) using a Eiger 4M detector at a sample-detector distance of 1.7 m and at a wavelength of λ = 0.088 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 sample at 10 mg/ml was injected onto a column at 4°C. One 2 second frame was collected. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.

SEC column = UNKNOWN. Sample injection volume = UNKNOWN. Flow rate = UNKNOWN

Acidic leucine-rich nuclear phosphoprotein 32 family member A (L60A mutant) (pp32)
Mol. type   Protein
Organism   Homo sapiens
Olig. state   Monomer
Mon. MW   28.5 kDa
 
UniProt   P39687 (1-249)
Sequence   FASTA