TY - JOUR
T1 - Neutron Laue diffraction experiments on a large unit cell
T2 - Concanavalin A complexed with methyl-α-D-glucopyranoside
AU - Joseph Kalb, A.
AU - Myles, Dean A.A.
AU - Habash, Jarjis
AU - Raftery, James
AU - Helliwell, John R.
PY - 2001
Y1 - 2001
N2 - A neutron Laue diffraction experiment on a complex of concanavalin A with methyl-α-D-glucopyranoside extensively soaked in D2O (space group I213, a = 167.8 Å), which resulted in 3.5 Å diffraction data, is described. In a programme of structural studies of crystalline saccharide complexes of concanavalin A, the unit cell of the cubic I213 complex of concanavalin A with methyl-α-D-glucopyranoside is one of the largest. With its cell edge of 167.8 Å and its asymmetric unit of molecular weight 50 kDa, it represents a challenge for current neutron diffraction technology. The size of the crystal used in this experiment, although large (4 × 3 x × 2 mm), was not the largest ever produced for this complex. The degree of spatial overlapping observed in the Laue experiment, however, suggests that use of larger crystals would be a disadvantage. On the basis of these observations, several technical improvements for macromolecular neutron crystallography are suggested.
AB - A neutron Laue diffraction experiment on a complex of concanavalin A with methyl-α-D-glucopyranoside extensively soaked in D2O (space group I213, a = 167.8 Å), which resulted in 3.5 Å diffraction data, is described. In a programme of structural studies of crystalline saccharide complexes of concanavalin A, the unit cell of the cubic I213 complex of concanavalin A with methyl-α-D-glucopyranoside is one of the largest. With its cell edge of 167.8 Å and its asymmetric unit of molecular weight 50 kDa, it represents a challenge for current neutron diffraction technology. The size of the crystal used in this experiment, although large (4 × 3 x × 2 mm), was not the largest ever produced for this complex. The degree of spatial overlapping observed in the Laue experiment, however, suggests that use of larger crystals would be a disadvantage. On the basis of these observations, several technical improvements for macromolecular neutron crystallography are suggested.
UR - http://www.scopus.com/inward/record.url?scp=20644459005&partnerID=8YFLogxK
U2 - 10.1107/S0021889801007245
DO - 10.1107/S0021889801007245
M3 - Article
AN - SCOPUS:20644459005
SN - 0021-8898
VL - 34
SP - 454
EP - 457
JO - Journal of Applied Crystallography
JF - Journal of Applied Crystallography
IS - 4
ER -