Structure basis for antitumor effect of aplyronine a |
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Authors: | Hirata Kunio Muraoka Shin Suenaga Kiyotake Kuroda Takeshi Kato Kenichi Tanaka Hiroshi Yamamoto Masaki Takata Masaki Yamada Kiyoyuki Kigoshi Hideo |
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Institution: | JASRI/SPring-8, 1-1-1 Kouto, Mikazuki-cho, Sayo-gun, Hyogo 679-5198 Japan. |
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Abstract: | Aplyronine A, isolated from the sea hare Aplysia kurodai, possesses an exceedingly potent antitumor effect in vivo and it is one of the promising candidates as an anticancer drug. This macrolide is known to depolymerize F-actin and inhibit the polymerization of actin by forming a 1:1 complex with monomeric actin. The first complex structure of actin-aplyronine A was determined via a synchrotron X-ray analysis at a 1.45 A resolution. As expected, aplyronine A binds to a hydrophobic cleft composed of subdomains 1 and 3 of actin by intercalating its aliphatic tail part into the actin molecule as do the other reported F-actin depolymerizing agents. Unexpectedly, this complex structure shows the specific structural features around the trimethylserine moiety, revealed as an important moiety of aplyronine A for cytotoxicity against HeLa cells. Combining this result and our previous one, the moiety should strongly relate to the specific biological activity of aplyronine A; i.e. a potent antitumor effect. |
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Keywords: | F-actin depolymerizing agent antitumor substance X-ray crystallography marine macrolide cytotoxicity |
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