Chaotic advection mixer for capturing transient states of diverse biological macromolecular systems with time-resolved small-angle X-ray scattering

Zielinski K, Katz A, Calvey G, Pabit S, Milano S, Aplin C, San Emeterio J, Cerione R, Pollack L, IUCrJ 10(3):363-375 (2023) DOI

SASDRM3 – Tissue Transglutaminase + Ca: 5min Equilibrium

Protein-glutamine gamma-glutamyltransferase 2
MWexperimental 126 kDa
MWexpected 77 kDa
VPorod 241 nm3
log I(s) 1.35×10-1 1.35×10-2 1.35×10-3 1.35×10-4
Protein-glutamine gamma-glutamyltransferase 2 small angle scattering data  s, nm-1
ln I(s)
Protein-glutamine gamma-glutamyltransferase 2 Guinier plot ln 1.36×10-1 Rg: 5.0 nm 0 (5.0 nm)-2 s2
(sRg)2I(s)/I(0)
Protein-glutamine gamma-glutamyltransferase 2 Kratky plot 1.104 0 3 sRg
Dmax: 27 nm

Data validation


There are no models related to this curve.

Synchrotron SAXS data from solutions of Tissue Transglutaminase + Ca: 5min Equilibrium in 20 mM HEPES, 100 mM NaCl, 10% glycerol, 1 mM DTT, pH 7.5 were collected on the ID7A1 BioSAXS / HP-Bio Beamline beam line at the Cornell High Energy Synchrotron Source (CHESS) storage ring (Ithaca, NY, USA) using a Eiger 4M detector at a wavelength of λ = 0.10972 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Solute concentrations ranging between 1.2 and 2 mg/ml were measured at 20°C. 10 successive 1 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.

TG (2 mg/mL) and CaCl2 (2 mM) were combined. The measurement was taken after ~5 minutes of interaction. Molecular Weight determined by Vc

Protein-glutamine gamma-glutamyltransferase 2 (TG2)
Mol. type   Protein
Organism   Homo sapiens
Olig. state   Unknown
Mon. MW   77.3 kDa
 
UniProt   P21980 (1-687)
Sequence   FASTA