beta PAK-interacting exchange factor may regulate actin cytoskeleton through interaction with actin
Experimental & Molecular Medicine
;
: 582-587, 2004.
Article
in English
| WPRIM
| ID: wpr-145920
ABSTRACT
p21-activated kinase (PAK)-interacting exchange factor (PIX) is known to be involved in regulation of Cdc42/Rac GTPases and PAK activity. PIX binds to the proline-rich region of PAK, and regulates biological events through activation of Cdc42/Rac GTPase. To further investigate the role of PIX we produced monoclonal antibodies (Mab) against beta PAK. Three clones; N-C6 against N-terminal half and C-A3 and C-B7 against C- terminal half of beta PAK were generated and characterized. N-C6 Mab detected beta PAK as a major band in most cell lines. C-A3 Mab recognizes GIT-binding domain (GBD), but it does not interfere with GIT binding to beta PAK. Using C-A3 Mab possible beta PAK interaction with actin in PC12 cells was examined. beta PAK Mab (C-A3) specifically precipitated actin of the PC12 cell lysates whereas actin Mab failed to immunoprecpitate beta PAK. Co-sedimentation of PC12 cell lysates with the polymerized F-actin resulted in the recovery of most of beta PAK in the cell lysates. These results suggest that beta PAK may not interact with soluble actin but with polymerized F-actin and revealed that beta PAK constitutes a functional complex with actin. These data indicate real usefulness of the beta PAK Mab in the study of beta PAK role(s) in regulation of actin cyoskeleton.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Actin Cytoskeleton
/
Actins
/
Protein Structure, Tertiary
/
Epitope Mapping
/
Cell Cycle Proteins
/
Guanine Nucleotide Exchange Factors
/
Cytoskeletal Proteins
/
Cell Line, Tumor
/
Immunoprecipitation
/
Antibodies, Monoclonal
Limits:
Animals
Language:
English
Journal:
Experimental & Molecular Medicine
Year:
2004
Type:
Article
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