Actin-targeting natural products: structures, properties and mechanisms of action

被引:160
作者
Allingham, J. S. [1 ]
Klenchin, V. A. [1 ]
Rayment, I. [1 ]
机构
[1] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
关键词
cytotoxic compound; anti-cancer drugs; actin filament dynamics; sequestering; capping; severing; filament stabilization;
D O I
10.1007/s00018-006-6157-9
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
Natural small-molecule inhibitors of actin cytoskeleton dynamics have long been recognized as valuable molecular probes for dissecting complex mechanisms of cellular function. More recently, their potential use as chemotherapeutic drugs has become a focus of scientific investigation. The primary focus of this review is the molecular mechanism by which different actin-targeting natural products function, with an emphasis on structural considerations of toxins for which high-resolution structural information of their interaction with actin is available. By comparing the molecular interactions made by different toxin families with actin, the structural themes of those that alter filament dynamics in similar ways can be understood. This provides a framework for novel synthetic-compound designs with tailored functional properties that could be applied in both research and clinical settings.
引用
收藏
页码:2119 / 2134
页数:16
相关论文
共 113 条
[1]   Structures of microfilament destabilizing toxins bound to actin provide insight into toxin design and activity [J].
Allingham, JS ;
Zampella, A ;
D'Auria, MV ;
Rayment, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (41) :14527-14532
[2]   Absolute stereochemistry of ulapualide A [J].
Allingham, JS ;
Tanaka, J ;
Marriott, G ;
Rayment, I .
ORGANIC LETTERS, 2004, 6 (04) :597-599
[3]   High rates of actin filament turnover in budding yeast and roles for actin in establishment and maintenance of cell polarity revealed using the actin inhibitor latrunculin-A [J].
Ayscough, KR ;
Stryker, J ;
Pokala, N ;
Sanders, M ;
Crews, P ;
Drubin, DG .
JOURNAL OF CELL BIOLOGY, 1997, 137 (02) :399-416
[4]   (-)-doliculide, a new macrocyclic depsipeptide enhancer of actin assembly [J].
Bai, RL ;
Covell, DG ;
Liu, CF ;
Ghosh, AK ;
Hamel, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (35) :32165-32171
[5]   Dolastatin 11, a marine depsipeptide, arrests cells at cytokinesis and induces hyperpolymerization of purified actin [J].
Bai, RL ;
Verdier-Pinard, P ;
Gangwar, S ;
Stessman, CC ;
McClure, KJ ;
Sausville, EA ;
Pettit, GR ;
Bates, RB ;
Hamel, E .
MOLECULAR PHARMACOLOGY, 2001, 59 (03) :462-469
[6]  
Belmont LD, 1999, J CELL SCI, V112, P1325
[7]   BISTRAMIDE-A, BISTRAMIDE-B, BISTRAMIDE-C, BISTRAMIE-D, AND BISTRAMIDE-K - A NEW CLASS OF BIOACTIVE CYCLIC POLYETHERS FROM LISSOCLINUM-BISTRATUM [J].
BIARD, JF ;
ROUSSAKIS, C ;
KORNPROBST, JM ;
GOUIFFESBARBIN, D ;
VERBIST, JF ;
COTELLE, P ;
FOSTER, MP ;
IRELAND, CM ;
DEBITUS, C .
JOURNAL OF NATURAL PRODUCTS, 1994, 57 (10) :1336-1345
[8]   SWINHOLIDE-A IS A MICROFILAMENT DISRUPTING MARINE TOXIN THAT STABILIZES ACTIN DIMERS AND SEVERS ACTIN-FILAMENTS [J].
BUBB, MR ;
SPECTOR, I ;
BERSHADSKY, AD ;
KORN, ED .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (08) :3463-3466
[9]   Polylysine induces an antiparallel actin dimer that nucleates filament assembly -: Crystal structure at 3.5-Å resolution [J].
Bubb, MR ;
Govindasamy, L ;
Yarmola, EG ;
Vorobiev, SM ;
Almo, SC ;
Somasundaram, T ;
Chapman, MS ;
Agbandje-McKenna, M ;
McKenna, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) :20999-21006
[10]   Effects of jasplakinolide on the kinetics of actin polymerization -: An explanation for certain in vivo observations [J].
Bubb, MR ;
Spector, I ;
Beyer, BB ;
Fosen, KM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (07) :5163-5170