ERROR 1
ERROR 1
ERROR 2
ERROR 2
ERROR 2
ERROR 2
ERROR 2
Password and Confirm password must match.
If you have an ACS member number, please enter it here so we can link this account to your membership. (optional)
ERROR 2
ACS values your privacy. By submitting your information, you are gaining access to C&EN and subscribing to our weekly newsletter. We use the information you provide to make your reading experience better, and we will never sell your data to third party members.
As vaccines against infectious diseases, nanoparticles with coatings that soak up unaltered bacterial protein toxins like a sponge could be more effective than heat-deactivated toxins, according to a report by Liangfang Zhang and coworkers at the University of California, San Diego (Nat. Nanotechnol. 2013, DOI: 10.1038/nnano.2013.254). Some bacterial toxins operate by embedding themselves in cell membranes, creating pores that leak cellular contents. Heating the toxins denatures them, thereby reducing their toxicity, but it also potentially reduces a vaccine’s effectiveness in stimulating the immune system to produce antibodies. Zhang’s team leveraged one bacterial toxin’s affinity for cell membranes to make a vaccine containing the unaltered toxin. The researchers coated plastic nanoparticles with red blood cell membranes embedded with α-hemolysin, a red-blood-cell-puncturing protein secreted by methicillin-resistant Staphylococcus aureus. Mice receiving the coated nanoparticles made more antibodies than mice receiving heat-treated α-hemolysin alone. Also, more mice receiving the nanoparticles survived direct injection of α-hemolysin. The nanoparticle membranes showed no sign of releasing the pore-forming toxins, which would be a problem in vaccines that use an unaltered toxin. The researchers say they could adapt the nanoparticles for toxins made by other bacteria.
Join the conversation
Contact the reporter
Submit a Letter to the Editor for publication
Engage with us on X