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PMID: 16909206 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

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

Cellular and molecular life sciences : CMLS ·Vol. 63 ·No. 18 ·2006-09-00 ·Pages 2119-34

Allingham JS, Klenchin VA, Rayment I

Abstract

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.

MeSH Terms
Actins/antagonists & inhibitors,metabolism Animals Biological Products Cell Movement/drug effects Cytoskeleton/metabolism GTP-Binding Proteins/antagonists & inhibitors,metabolism Humans Marine Toxins Microfilament Proteins/antagonists & inhibitors,metabolism Protein Binding Signal Transduction
Chemicals
Actins Biological Products Marine Toxins Microfilament Proteins GTP-Binding Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Allingham J S
Department of Biochemistry, University of Wisconsin, 433 Babcock Drive, Madison, Wisconsin 53706, USA.
Klenchin V A
Rayment I
Article Info
Journal
Cellular and molecular life sciences : CMLS
Abbr.
Cell Mol Life Sci
ISSN
1420-682X
Published
2006-09-00
Pages
2119-34
Language
English
Region
Switzerland
NLM ID
9705402
Subset
IM
Grants
NIAMS NIH HHS · AR35186 · United States
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