Antiviral signalling by a cyclic nucleotide activated CRISPR protease.

Rouillon C, Schneberger N, Chi H, Blumenstock K, Da Vela S, Ackermann K, Moecking J, Peter MF, Boenigk W, Seifert R, Bode BE, Schmid-Burgk JL, Svergun D, Geyer M, White MF, Hagelueken G, Nature 614(7946):168-174 (2023) Europe PMC

SASDQM4 – CRISPR associated Lon protease (CalpL)

SAVED domain-containing protein
MWexperimental 53 kDa
MWexpected 58 kDa
VPorod 80 nm3
log I(s) 7.47×102 7.47×101 7.47×100 7.47×10-1
SAVED domain-containing protein small angle scattering data  s, nm-1
ln I(s)
SAVED domain-containing protein Guinier plot ln 7.48×102 Rg: 3.1 nm 0 (3.1 nm)-2 s2
(sRg)2I(s)/I(0)
SAVED domain-containing protein Kratky plot 1.104 0 √3 sRg
p(r)
SAVED domain-containing protein pair distance distribution function Rg: 3.2 nm 0 Dmax: 10.3 nm

Data validation

Fits and models

log I(s)
 s, nm-1
SAVED domain-containing protein DAMMIF model
log I(s)
 s, nm-1
SAVED domain-containing protein MONSA model
Synchrotron SAXS data from solutions of CRISPR associated Lon protease (CalpL) in 20 mM Tris, 50 mM NaCl, pH 8 were collected on the EMBL P12 beam line at PETRA III (DESY, Hamburg, Germany) using a Pilatus 6M detector at a sample-detector distance of 3.1 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 40.00 μl sample at 8.8 mg/ml was injected at a 0.30 ml/min flow rate onto a GE Superdex 200 Increase 5/150 column at 20°C. 900 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.

SAVED domain-containing protein (CalpL)
Mol. type   Protein
Organism   Sulfurihydrogenibium sp. (strain YO3AOP1)
Olig. state   Monomer
Mon. MW   57.7 kDa
 
UniProt   B2V8L9 (2-496)
Sequence   FASTA