Skip to main content
U.S. flag

An official website of the United States government

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Ultrasound programmable hydrogen-bonded organic frameworks for sono-chemogenetics

Published

Author(s)

Wenliang Wang, Yanshu Shi, Wenrui Chai, Kai Tang, Ilya Pyatnitskiy, Yi Xie, Xiangping Liu, Weilong He, Jinmo Jeong, Ju-Chun Hsieh, Anakaren Lozano, Brinkley Artman, Xi Shi, Nicole Hoefer, Binita Shrestha, Noah Stern, Wei Zhou, David McComb, Tyrone Porter, Graeme Henkelman, Banglin Chen, Huiliang Wang

Abstract

The precise control of mechanochemical activation within deep tissues via non-invasive ultrasound holds profound implications for advancing our understanding of fundamental biomedical sciences and revolutionizing disease treatments. However, a theory-guided mechanoresponsive materials system with well-defined ultrasound activation has yet to be explored. Here we present the concept of using porous hydrogen-bonded organic frameworks (HOFs) as toolkits for focused ultrasound programmably triggered drug activation to control specific cellular events in the deep brain, through on-demand scission of the supramolecular interactions. A theoretical model is developed to potentially visualize the mechanochemical scission and ultrasound mechanics, providing valuable guidelines for the rational design of mechanoresponsive materials at the molecular level to achieve programmable and spatiotemporal activation control. To demonstrate the practicality of this approach, we encapsulate designer drug clozapine N-40 oxide (CNO) into the optimal HOF particles for FUS gated release to activate engineered G-protein-coupled receptors in the mice and rats ventral tegmental area (VTA), and hence achieved targeted neural circuits modulation even at depth 9 mm with a latency of seconds. This work demonstrates the capability of ultrasound to precisely control molecular interaction and develops ultrasound programmable HOFs to minimally invasive and spatiotemporally control cellular events, thereby facilitating the establishment of precise molecular therapeutic possibilities. We anticipate that this research could serve as a source of inspiration for precise and non-invasive molecular manipulation techniques, potentially applicable in programming molecular robots to achieve sophisticated control over cellular events in deep tissues.
Citation
Nature

Keywords

Porous material, drug delivery

Citation

Wang, W. , Shi, Y. , Chai, W. , Tang, K. , Pyatnitskiy, I. , Xie, Y. , Liu, X. , He, W. , Jeong, J. , Hsieh, J. , Lozano, A. , Artman, B. , Shi, X. , Hoefer, N. , Shrestha, B. , Stern, N. , Zhou, W. , McComb, D. , Porter, T. , Henkelman, G. , Chen, B. and Wang, H. (2023), Ultrasound programmable hydrogen-bonded organic frameworks for sono-chemogenetics, Nature (Accessed December 8, 2024)

Issues

If you have any questions about this publication or are having problems accessing it, please contact reflib@nist.gov.

Created December 9, 2023, Updated August 19, 2024