308 496

Cited 0 times in

Scaffolding Protein in Ca2+ signaling

Authors
 Hong Jeong Hee  ;  Kim Min Seuk  ;  Shin Dong Min  ;  Lee Syng-Ill  ;  Joe Hae 
Citation
 International Journal of Oral Biology, Vol.28(3) : 75-80, 2003 
Journal Title
International Journal of Oral Biology
ISSN
 1226-7155 
Issue Date
2003
MeSH
Scaffolding Protein ; ca〖^〗2+ Signaling ; Homer Proteins
Keywords
Scaffolding Protein ; ca〖^〗2+ Signaling ; Homer Proteins
Abstract
Polarized expression of signaling complexes requires retention of the proteins in the microdomains, which expression and retention are aided by scaffolding proteins. Little or 1 m information is available as to the nature of scaffoldini: proteins in CaZ+ signaling in non-excitable cells. Recently 1 lomers are regarded as an attractive candidate of scaffoldin I : protein in Ca 2+ signaling, because Homers bind G protei . coupled receptors (GPCRs), IP3 receptors, ryanodinc receptors and TRP channels. However, their role in CaZ+ si: haling in vivo and in vitro is not known. The data suggested by our work using Homer knock-out mice demonstr ate a novel, unexpected function of Homer proteins, in that RGS proteins and PLCP GTPase Activatin;: activities are regulated and provide a molecular mechanis 1 a for tuning signal intensity generated by GPCRs and thus the characteristics of intracellualr CaZ+ oscillations. In addition, Homer protein facilitates a physical association between TRP channels and IP3 receptor that is required `Dr the TRP channel in response to signals, which provide t; .e evidence for a conformational coupling model with an e:;;ential role for interaction between TRP channels and intral ellular CaZ+ release channels.
Files in This Item:
T200301136.pdf Download
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Biology (구강생물학교실) > 1. Journal Papers
Yonsei Authors
Shin, Dong Min(신동민) ORCID logo https://orcid.org/0000-0001-6042-0435
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/113219
사서에게 알리기
  feedback

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse

Links