Alternative splicing controls teneurin-3 compact dimer formation for neuronal recognition

Gogou C, Beugelink J, Frias C, Kresik L, Jaroszynska N, Drescher U, Janssen B, Hindges R, Meijer D, Nature Communications 15(1) (2024) DOI

SASDT33 – Teneurin-3 A1B1 isoform in 2 mM calcium - 0.31 mg/mL

Isoform A1B1 of Teneurin-3
MWI(0) 555 kDa
MWexpected 545 kDa
VPorod 1129 nm3
log I(s) 1.71×102 1.71×101 1.71×100 1.71×10-1
Isoform A1B1 of Teneurin-3 small angle scattering data  s, nm-1
ln I(s)
Isoform A1B1 of Teneurin-3 Guinier plot ln 1.72×102 Rg: 7.9 nm 0 (7.9 nm)-2 s2
(sRg)2I(s)/I(0)
Isoform A1B1 of Teneurin-3 Kratky plot 1.104 0 3 sRg
Dmax: 33 nm

Data validation


There are no models related to this curve.

Synchrotron SAXS data from solutions of Teneurin-3 A1B1 isoform in 20 mM HEPES, 150 mM NaCl, 2 mM CaCl2, pH 7.8 were collected on the BM29 beam line at the ESRF (Grenoble, France) using a Pilatus3 2M detector at a wavelength of λ = 0.099188 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). One solute concentration of 0.31 mg/ml was 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.

Sample detector distance = UNKNOWN

Isoform A1B1 of Teneurin-3 (Ten3-A1B1)
Mol. type   Protein
Organism   Mus musculus
Olig. state   Dimer
Mon. MW   272.4 kDa
 
UniProt   Q9WTS6-1 (343-2715)
Sequence   FASTA