Scientific Article
previous document  unige:11208  next document
add to browser collection

Ca2+ regulation of interactions between endoplasmic reticulum chaperones

Corbett, Elaine F.
Oikawa, Kim
Tessier, Daniel C.
Kay, Cyril
Bergeron, John J.
Thomas, David Y.
show hidden authors show all authors [1 - 9]
Published in Journal of Biological Chemistry. 1999, vol. 274, no. 10, p. 6203-6211
Abstract Casade Blue (CB), a fluorescent dye, was used to investigate the dynamics of interactions between endoplasmic reticulum (ER) lumenal chaperones including calreticulin, protein disulfide isomerase (PDI), and ERp57. PDI and ERp57 were labeled with CB, and subsequently, we show that the fluorescence intensity of the CB-conjugated proteins changes upon exposure to microenvironments of a different polarity. CD analysis of the purified proteins revealed that changes in the fluorescence intensity of CB-ERp57 and CB-PDI correspond to conformational changes in the proteins. Using this technique we demonstrate that PDI interacts with calreticulin at low Ca2+ concentration (below 100 microM), whereas the protein complex dissociates at >400 microM Ca2+. These are the Ca2+ concentrations reminiscent of Ca2+ levels found in empty or full ER Ca2+ stores. The N-domain of calreticulin interacts with PDI, but Ca2+ binding to the C-domain of the protein is responsible for Ca2+ sensitivity of the interaction. ERp57 also interacts with calreticulin through the N-domain of the protein. Initial interaction between these proteins is Ca2+-independent, but it is modulated by Ca2+ binding to the C-domain of calreticulin. We conclude that changes in ER lumenal Ca2+ concentration may be responsible for the regulation of protein-protein interactions. Calreticulin may play a role of Ca2+ "sensor" for ER chaperones via regulation of Ca2+-dependent formation and maintenance of structural and functional complexes between different proteins involved in a variety of steps during protein synthesis, folding, and post-translational modification.
Keywords AnimalsCalcium/ metabolismDogsEndoplasmic Reticulum/ metabolismFluorescent DyesMolecular Chaperones/chemistry/ metabolismProtein BindingProtein ConformationProtein Processing, Post-Translational
Stable URL
Full text
Article - document accessible for UNIGE members only Limited access to UNIGE
Other version:
PMID: 10037706
106 hits and 2 downloads since 2010-08-27
Export document
Format :
Citation style :