4.8 Article

Acoustically triggered mechanotherapy using genetically encoded gas vesicles

Journal

NATURE NANOTECHNOLOGY
Volume 16, Issue 12, Pages 1403-U147

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41565-021-00971-8

Keywords

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Funding

  1. David and Lucile Packard Fellowship for Science and Engineering
  2. Heritage Medical Research Institute
  3. European Union [792866]
  4. Lester Deutsch Fellowship
  5. Amgen scholars programme
  6. NSF Graduate Research Fellowship
  7. P.D. Soros Fellowship
  8. Human Frontiers Science Program Cross-Disciplinary Fellowship
  9. Marie Curie Actions (MSCA) [792866] Funding Source: Marie Curie Actions (MSCA)

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Recent advancements in molecular engineering and synthetic biology have enabled the development of biomolecular and cell-based therapies with high molecular specificity, but limited spatiotemporal control. Gas vesicles, a genetically encodable air-filled protein nanostructure, can be engineered to deliver potent mechanical effects at specific locations inside the body through ultrasound-induced inertial cavitation. This capability has potential applications in remotely actuated cell-killing and tissue-disrupting agents, demonstrating the therapeutic potential of gas vesicles under focused ultrasound actuation.
Recent advances in molecular engineering and synthetic biology provide biomolecular and cell-based therapies with a high degree of molecular specificity, but limited spatiotemporal control. Here we show that biomolecules and cells can be engineered to deliver potent mechanical effects at specific locations inside the body through ultrasound-induced inertial cavitation. This capability is enabled by gas vesicles, a unique class of genetically encodable air-filled protein nanostructures. We show that low-frequency ultrasound can convert these biomolecules into micrometre-scale cavitating bubbles, unleashing strong local mechanical effects. This enables engineered gas vesicles to serve as remotely actuated cell-killing and tissue-disrupting agents, and allows genetically engineered cells to lyse, release molecular payloads and produce local mechanical damage on command. We demonstrate the capabilities of biomolecular inertial cavitation in vitro, in cellulo and in vivo, including in a mouse model of tumour-homing probiotic therapy. Gas vesicles are air-filled protein nanostructures naturally expressed by certain bacteria and archaea to achieve cellular buoyancy. Here the authors show that, under the stimulation of pulsed ultrasound, targeted gas vesicles and gas vesicles expressed in genetically modified bacteria and mammalian cells release nanobubbles that, collapsing, lead to controlled mechanical damage of the surrounding biological milieu, demonstrating that, under focused ultrasound actuation, gas vesicles have potential applications as therapeutic agents.

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