13-Deoxytedanolide, a marine sponge-derived antitumor macrolide, binds to the 60S large ribosomal subunit

被引:62
作者
Nishimura, S
Matsunaga, S
Yoshida, M
Hirota, H
Yokoyama, S
Fusetani, N [1 ]
机构
[1] Univ Tokyo, Grad Sch Agr & Life Sci, Lab Aquat Nat Prod Chem, Bunkyo Ku, Tokyo 1138657, Japan
[2] RIKEN, Genom Sci Ctr, Yokohama, Kanagawa 2300045, Japan
[3] RIKEN, Chem Genet Lab, Wako, Saitama 3510198, Japan
关键词
13-deoxytedanlide; antitumor macrolide; ribosome; pederin;
D O I
10.1016/j.bmc.2004.10.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
13-Deoxytedanolide is a potent antitumor macrolide isolated from the marine sponge Mycale adhaerens. In spite of its remarkable activity, the mode of action of 13-deoxytedanolide has not been elucidated. [11-H-3]-(11S)-13-Deoxydihydrotedanolide derived from the macrolide was used for identifying the target molecule from the yeast cell lysate. Fractionation of the binding protein revealed that the labeled 13-deoxytedanolide derivative strongly bound to the 80S ribosome as well as to the 60S large subunit, but not to the 40S small subunit. In agreement with this observation, 13-deoxytedanolide efficiently inhibited the polypeptide elongation. Interestingly, competition studies demonstrated that 13-deoxytedanolide shared the binding site on the 60S large subunit with pederin and its marine-derived analogues. These results indicate that 13-deoxytedanolide is a potent protein synthesis inhibitor and is the first macrolide to inhibit the eukaryotic ribosome. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:449 / 454
页数:6
相关论文
共 38 条
[1]   Development and characterization of a reconstituted yeast translation initiation system [J].
Algire, MA ;
Maag, D ;
Savio, P ;
Acker, MG ;
Tarun, SZ ;
Sachs, AB ;
Asano, K ;
Nielsen, KH ;
Olsen, DS ;
Phan, L ;
Hinnebusch, AG ;
Lorsch, JR .
RNA, 2002, 8 (03) :382-397
[2]   RIBOSOME CHANGES DURING TRANSLATION [J].
BARBACID, M ;
VAZQUEZ, D .
JOURNAL OF MOLECULAR BIOLOGY, 1975, 93 (04) :449-463
[3]  
BURRES NS, 1989, CANCER RES, V49, P2935
[4]  
CREWS CM, 1994, J BIOL CHEM, V269, P15411
[5]  
Cundliffe E., 1981, MOL BASIS ANTIBIOTIC, V2nd, P402
[6]  
FERNANDEZMUNOZ R, 1971, METHOD ENZYMOL, V20, P481
[7]   ISOLATION AND STRUCTURE ELUCIDATION OF RITTERAZINE-B AND RITTERAZINE-C, HIGHLY CYTOTOXIC DIMERIC STEROIDAL ALKALOIDS, FROM THE TUNICATE RITTERELLA-TOKIOKA [J].
FUKUZAWA, S ;
MATSUNAGA, S ;
FUSETANI, N .
JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (03) :608-614
[8]   BIOACTIVE MARINE METABOLITES .35. CYTOTOXIC METABOLITES OF THE MARINE SPONGE MYCALE-ADHAERENS LAMBE [J].
FUSETANI, N ;
SUGAWARA, T ;
MATSUNAGA, S ;
HIROTA, H .
JOURNAL OF ORGANIC CHEMISTRY, 1991, 56 (16) :4971-4974
[9]   BIOACTIVE MARINE METABOLITES SERIES .41. THEOPEDERINS-A-E, POTENT ANTITUMOR METABOLITES FROM A MARINE SPONGE, THEONELLA SP [J].
FUSETANI, N ;
SUGAWARA, T ;
MATSUNAGA, S .
JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (14) :3828-3832
[10]   Structures of five antibiotics bound at the peptidyl transferase center of the large ribosomal subunit [J].
Hansen, JL ;
Moore, PB ;
Steitz, TA .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 330 (05) :1061-1075