Selective light-triggered release of DNA from gold nanorods switches blood clotting on and off

PLoS One. 2013 Jul 24;8(7):e68511. doi: 10.1371/journal.pone.0068511. Print 2013.

Abstract

Blood clotting is a precise cascade engineered to form a clot with temporal and spatial control. Current control of blood clotting is achieved predominantly by anticoagulants and thus inherently one-sided. Here we use a pair of nanorods (NRs) to provide a two-way switch for the blood clotting cascade by utilizing their ability to selectively release species on their surface under two different laser excitations. We selectively trigger release of a thrombin binding aptamer from one nanorod, inhibiting blood clotting and resulting in increased clotting time. We then release the complementary DNA as an antidote from the other NR, reversing the effect of the aptamer and restoring blood clotting. Thus, the nanorod pair acts as an on/off switch. One challenge for nanobiotechnology is the bio-nano interface, where coronas of weakly adsorbed proteins can obscure biomolecular function. We exploit these adsorbed proteins to increase aptamer and antidote loading on the nanorods.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Aptamers, Nucleotide / chemistry
  • Aptamers, Nucleotide / pharmacology
  • Blood Coagulation / drug effects
  • Blood Coagulation / radiation effects*
  • DNA / chemistry*
  • DNA / pharmacology*
  • Gold / chemistry*
  • Humans
  • Light*
  • Metal Nanoparticles / chemistry*
  • Nanotechnology
  • Nanotubes / chemistry*

Substances

  • Aptamers, Nucleotide
  • thrombin aptamer
  • Gold
  • DNA

Grants and funding

This work was funded by the National Science Foundation grant# DMR #0906838. http://www.nsf.gov/. HdP was supported by a fellowship from La Caixa Foundation (Spain). http://obrasocial.lacaixa.es/laCaixaFoundation/home_en.html. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.