TY - JOUR
T1 - A novel action of terpendole E on the motor activity of mitotic kinesin Eg5
AU - Nakazawa, Junko
AU - Yajima, Junichiro
AU - Usui, Takeo
AU - Ueki, Masashi
AU - Takatsuki, Akira
AU - Imoto, Masaya
AU - Toyoshima, Yoko Y.
AU - Osada, Hiroyuki
N1 - Funding Information:
The authors are grateful to Drs. S. Omura and H. Tomoda (Kitasato University) for the gift of terpendole C as an authentic sample. We also acknowledged Dr. G. Okada (RIKEN Institute) for taxonomic study of the producer strain, and Drs E. Schiebel and K. Labib (CRC Paterson Institute) for helpful comments on the manuscripts. This study was supported by a Grant of Bioarchitect Basic Research in RIKEN, and a grant from the Ministry of Education, Culture, Sports, Science, and Technology.
PY - 2003/2/1
Y1 - 2003/2/1
N2 - To reveal the mechanism of mitosis, the development of M phase-specific inhibitors is an important strategy. We have been screening microbial products to find specific M phase inhibitors that do not directly target tubulins, and rediscovered terpendole E (TerE) as a novel Eg5 inhibitor. TerE did not affect microtubule integrity in interphase, but induced formation of a monoastral spindle in M phase. TerE inhibited both motor and microtubule-stimulated ATPase activities of human Eg5, but did not affect conventional kinesin from either Drosophila or bovine brain. Although terpendoles have been reported as inhibitors of acyl-CoA:cholesterol O-acyltransferase (ACAT), the Eg5 inhibitory activity of TerE was independent of ACAT inhibition. Taken together, we demonstrate that TerE is a novel Eg5 inhibitor isolated from a fungal strain.
AB - To reveal the mechanism of mitosis, the development of M phase-specific inhibitors is an important strategy. We have been screening microbial products to find specific M phase inhibitors that do not directly target tubulins, and rediscovered terpendole E (TerE) as a novel Eg5 inhibitor. TerE did not affect microtubule integrity in interphase, but induced formation of a monoastral spindle in M phase. TerE inhibited both motor and microtubule-stimulated ATPase activities of human Eg5, but did not affect conventional kinesin from either Drosophila or bovine brain. Although terpendoles have been reported as inhibitors of acyl-CoA:cholesterol O-acyltransferase (ACAT), the Eg5 inhibitory activity of TerE was independent of ACAT inhibition. Taken together, we demonstrate that TerE is a novel Eg5 inhibitor isolated from a fungal strain.
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U2 - 10.1016/S1074-5521(03)00020-6
DO - 10.1016/S1074-5521(03)00020-6
M3 - Article
C2 - 12618185
AN - SCOPUS:0242515795
SN - 1074-5521
VL - 10
SP - 131
EP - 137
JO - Chemistry and Biology
JF - Chemistry and Biology
IS - 2
ER -