» Articles » PMID: 25868452

Engineered Nanoparticles Mimicking Cell Membranes for Toxin Neutralization

Overview
Specialty Pharmacology
Date 2015 Apr 15
PMID 25868452
Citations 55
Authors
Affiliations
Soon will be listed here.
Abstract

Protein toxins secreted from pathogenic bacteria and venomous animals rely on multiple mechanisms to overcome the cell membrane barrier to inflict their virulence effect. A promising therapeutic concept toward developing a broadly applicable anti-toxin platform is to administer cell membrane mimics as decoys to sequester these virulence factors. As such, lipid membrane-based nanoparticulates are an ideal candidate given their structural similarity to cellular membranes. This article reviews the virulence mechanisms employed by toxins at the cell membrane interface and highlights the application of cell-membrane mimicking nanoparticles as toxin decoys for systemic detoxification. In addition, the implication of particle/toxin nanocomplexes in the development of toxoid vaccines is discussed.

Citing Articles

Engineered Biomimetic Platelet Membrane-Coated Nanoparticles Block Cytotoxicity and Protect Against Lethal Systemic Infection.

Kim J, Uchiyama S, Gong H, Stream A, Zhang L, Nizet V Engineering (Beijing). 2024; 7(8):1149-1156.

PMID: 39449819 PMC: 11501092. DOI: 10.1016/j.eng.2020.09.013.


Bacterial pore-forming toxin pneumolysin drives pathogenicity through host extracellular vesicles released during infection.

Parveen S, Bhat C, Sagilkumar A, Aziz S, Arya J, Dutta A iScience. 2024; 27(8):110589.

PMID: 39211544 PMC: 11357855. DOI: 10.1016/j.isci.2024.110589.


Functionally Designed Nanovaccines against SARS-CoV-2 and Its Variants.

Xi Y, Ma R, Li S, Liu G, Liu C Vaccines (Basel). 2024; 12(7).

PMID: 39066402 PMC: 11281565. DOI: 10.3390/vaccines12070764.


Biomimetic Hydrogel Strategies for Cancer Therapy.

Alshehri A, Wilson Jr O Gels. 2024; 10(7).

PMID: 39057460 PMC: 11275631. DOI: 10.3390/gels10070437.


Design Strategies for Cellular Nanosponges as Medical Countermeasures.

Wang S, Wang D, Kai M, Shen W, Sun L, Gao W BME Front. 2023; 4:0018.

PMID: 37849681 PMC: 10521708. DOI: 10.34133/bmef.0018.


References
1.
Gouaux E . alpha-Hemolysin from Staphylococcus aureus: an archetype of beta-barrel, channel-forming toxins. J Struct Biol. 1998; 121(2):110-22. DOI: 10.1006/jsbi.1998.3959. View

2.
Johannes L, Romer W . Shiga toxins--from cell biology to biomedical applications. Nat Rev Microbiol. 2009; 8(2):105-16. DOI: 10.1038/nrmicro2279. View

3.
Parodi A, Quattrocchi N, van de Ven A, Chiappini C, Evangelopoulos M, Martinez J . Synthetic nanoparticles functionalized with biomimetic leukocyte membranes possess cell-like functions. Nat Nanotechnol. 2012; 8(1):61-8. PMC: 3751189. DOI: 10.1038/nnano.2012.212. View

4.
Forouhar F, Huang W, Liu J, Chien K, Wu W, Hsiao C . Structural basis of membrane-induced cardiotoxin A3 oligomerization. J Biol Chem. 2003; 278(24):21980-8. DOI: 10.1074/jbc.M208650200. View

5.
Harvey A, Karlsson E . Dendrotoxin from the venom of the green mamba, Dendroaspis angusticeps. A neurotoxin that enhances acetylcholine release at neuromuscular junction. Naunyn Schmiedebergs Arch Pharmacol. 1980; 312(1):1-6. DOI: 10.1007/BF00502565. View