Document Detail


Drug targeting: learning from toxin entry and trafficking in mammalian cells.
MedLine Citation:
PMID:  20047149     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A significant number of therapeutic targets reside inside cells and intracellular organelles. Therapeutics therefore must be able to gain access to cellular compartments, and be able to interact specifically with a given molecule to exert a desired effect. Many naturally occurring toxins perform such targeting with apparent ease, making them excellent paradigms for the delivery of therapeutics to the cell interior. By studying the mechanisms of cell entry, trafficking and modes of toxicity of these model delivery vectors, researchers can decipher how cells transport both endogenous molecules and exogenously applied therapeutics inside cells. Perhaps more importantly, the exploitation of cell binding and trafficking motifs could allow a therapeutic to target specifically, traffic within and escape from cellular compartments; in addition, toxic domains can be used to disrupt cell function specifically for therapeutic purposes. This review provides an overview of recent developments in the understanding of toxin targeting and trafficking, and discusses how these developments could result in opportunities for the design of more specific and efficient systems for therapeutic targeting.
Authors:
Robert A Spooner; Peter Watson
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review    
Journal Detail:
Title:  Current opinion in drug discovery & development     Volume:  13     ISSN:  2040-3437     ISO Abbreviation:  Curr Opin Drug Discov Devel     Publication Date:  2010 Jan 
Date Detail:
Created Date:  2010-01-04     Completed Date:  2010-03-01     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100887519     Medline TA:  Curr Opin Drug Discov Devel     Country:  England    
Other Details:
Languages:  eng     Pagination:  86-95     Citation Subset:  IM    
Affiliation:
Cardiff University, School of Biosciences, Museum Avenue, Cardiff, CF10 3AX, UK. R.A.Spooner@warwick.ac.uk
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MeSH Terms
Descriptor/Qualifier:
Animals
Cells / metabolism*,  ultrastructure
Drug Delivery Systems*
Endoplasmic Reticulum / metabolism
Humans
Models, Biological
Nanoparticles
Plasma / metabolism
Protein Transport / drug effects,  physiology
Small Molecule Libraries
Toxins, Biological / metabolism*
Grant Support
ID/Acronym/Agency:
080566Z/06/Z//Wellcome Trust
Chemical
Reg. No./Substance:
0/Small Molecule Libraries; 0/Toxins, Biological

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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