Published June 22, 2007 | Version v1
Journal article

Analysis of internal motions of interleukin-13 variant associated with severe bronchial asthma using 15N NMR relaxation measurements

  • 1. Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka 812-8582 (Japan)
  • 2. Research Group for Molecular Structural Biology, Quantum Beam Science Directorate, Japan Atomic Energy Agency, 2-4 Shirakata-Shirane, Tokai, Ibaraki 319-1195 (Japan)
  • 3. Division of Medical Biochemistry, Department of Biomolecular Sciences, Center for Comprehensive Community Medicine, Saga Medical School, Saga 849-8501 (Japan)
  • 4. Faculty of Biotechnology and Life Science, Sojo University, Kumamoto 860-0082 (Japan)

Description

The single nucleotide polymorphism interleukin-13 (IL-13) R110Q is associated with severe bronchial asthma because its lower affinity leads to the augmentation of local IL-13 concentration, resulting in an increase in the signal transduction via IL-13R. Since the mutation site does not directly bind to IL-13Rα2, we carried out NMR relaxation analyses of the wild-type IL-13 and IL-13-R110Q in order to examine whether the R110Q mutation affects the internal motions in IL-13 molecules. The results showed that the internal motion in the micro- to millisecond time scale on helix D, which is suggested to be important for the interaction between IL-13 and IL-13Rα2, is increased in IL-13-R110Q compared with that in the wild-type IL-13. It therefore appears that the difference in the internal motions on helix D between the wild-type IL-13 and IL-13-R110Q may be involved in their affinity differences with IL-13Rα2

Additional details

Identifiers

DOI
10.1016/j.bbrc.2007.04.128;
PII
S0006-291X(07)00855-8;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
358
Journal Issue
1
Journal Page Range
p. 292-297
ISSN
0006-291X
CODEN
BBRCA9

Optional Information

Copyright
Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.