TY - JOUR
T1 - Photosensitivity of neurons enabled by cell-targeted gold nanoparticles
AU - Carvalho-de-Souza, João L.
AU - Treger, Jeremy S.
AU - Dang, Bobo
AU - Kent, Stephen B.H.
AU - Pepperberg, David R.
AU - Bezanilla, Francisco
N1 - Funding Information:
We thank Dr. Karol S. Bruzik, Dr. Pavel Y. Savechenkov, and Dr. Christoph H. Grein (University of Illinois at Chicago), Dr. Lan Yue (University of Southern California), and Dr. Tijana Rajh (Argonne National Laboratory) for helpful discussions during the course of this study. We are especially indebted to Dr. Deborah Nelson and Dr. Vladimir Riazanski (University of Chicago) for their assistance in harvesting brain slices and guidance on their use. This work was supported by NIH grants EY023430, GM030376, and EY001792; the Beckman Initiative for Macular Research (Los Angeles, CA); and Research to Prevent Blindness, (New York, NY).
Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2015/4/8
Y1 - 2015/4/8
N2 - Unmodified neurons can be directly stimulated with light to produce action potentials, but such techniques have lacked localization of the delivered light energy. Here we show that gold nanoparticles can be conjugated to high-avidity ligands for a variety of cellular targets. Once bound to a neuron, these particles transduce millisecond pulses of light into heat, which changes membrane capacitance, depolarizing the cell and eliciting action potentials. Compared to non-functionalized nanoparticles, ligand-conjugated nanoparticles highly resist convective washout and enable photothermal stimulation with lower delivered energy and resulting temperature increase. Ligands targeting three different membrane proteins were tested; all showed similar activity and washout resistance. This suggests that many types of ligands can be bound to nanoparticles, preserving ligand and nanoparticle function, and that many different cell phenotypes can be targeted by appropriate choice of ligand. The findings have applications as an alternative to optogenetics and potentially for therapies involving neuronal photostimulation.
AB - Unmodified neurons can be directly stimulated with light to produce action potentials, but such techniques have lacked localization of the delivered light energy. Here we show that gold nanoparticles can be conjugated to high-avidity ligands for a variety of cellular targets. Once bound to a neuron, these particles transduce millisecond pulses of light into heat, which changes membrane capacitance, depolarizing the cell and eliciting action potentials. Compared to non-functionalized nanoparticles, ligand-conjugated nanoparticles highly resist convective washout and enable photothermal stimulation with lower delivered energy and resulting temperature increase. Ligands targeting three different membrane proteins were tested; all showed similar activity and washout resistance. This suggests that many types of ligands can be bound to nanoparticles, preserving ligand and nanoparticle function, and that many different cell phenotypes can be targeted by appropriate choice of ligand. The findings have applications as an alternative to optogenetics and potentially for therapies involving neuronal photostimulation.
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U2 - 10.1016/j.neuron.2015.02.033
DO - 10.1016/j.neuron.2015.02.033
M3 - Article
C2 - 25772189
AN - SCOPUS:84928886571
SN - 0896-6273
VL - 86
SP - 207
EP - 217
JO - Neuron
JF - Neuron
IS - 1
ER -