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PMID: 8163010 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cell cycle-dependent association of Gag-Mil and hsp90.

FEBS letters ·Vol. 343 ·No. 1 ·1994-04-18 ·Pages 15-21

Lovrić J, Bischof O, Moelling K

Abstract

Immunoprecipitated p100Gag-Mil protein kinase from MH2-transformed quail embryo fibroblasts is associated with an 89 kDa protein. The molar ratio between p89 and Gag-Mil in the immunocomplex is 0.72, indicating that the majority of Gag-Mil is complexed with p89. During mitosis part of Gag-Mil is shifted to a form with reduced electrophoretic mobility, p102Gag-Mil. Appearance of p102Gag-Mil leads to a reduced association with p89 indicating that p102 is not associated with p89. Microsequencing of p89 isolated from immunoprecipitates of Gag-Mil identified the protein as the quail homologue of chicken hsp90. Our results show that p100Gag-Mil is associated with hsp90 with a high stoichiometry and that upshifted p102Gag-Mil is released from the complex with hsp90.

MeSH Terms
Amino Acid Sequence Animals Cell Cycle Cell Line, Transformed Gene Products, gag/metabolism Heat-Shock Proteins/metabolism Humans Molecular Sequence Data Protein Serine-Threonine Kinases/metabolism Proto-Oncogene Proteins/metabolism Proto-Oncogene Proteins c-raf Quail
Chemicals
Gene Products, gag Heat-Shock Proteins Proto-Oncogene Proteins Protein Serine-Threonine Kinases Proto-Oncogene Proteins c-raf
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Lovrić J
Max-Planck-Institut für Molekulare Genetik, Abt. Schuster, Berlin (Dahlem), Germany.
Bischof O
Moelling K
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1994-04-18
Pages
15-21
Language
English
Region
England
NLM ID
0155157
Subset
IM
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