TY - JOUR
T1 - Analysis of internal motions of interleukin-13 variant associated with severe bronchial asthma using 15N NMR relaxation measurements
AU - Yoshida, Yuichiro
AU - Ohkuri, Takatoshi
AU - Takeda, Chika
AU - Kuroki, Ryota
AU - Izuhara, Kenji
AU - Imoto, Taiji
AU - Ueda, Tadashi
PY - 2007/6/22
Y1 - 2007/6/22
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=34248179165&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=34248179165&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2007.04.128
DO - 10.1016/j.bbrc.2007.04.128
M3 - Article
C2 - 17482144
AN - SCOPUS:34248179165
SN - 0006-291X
VL - 358
SP - 292
EP - 297
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 1
ER -