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Active NON-SBIR/STTR RPGS NIH (US)

Next-generation design of acoustic reporter genes with optimal assembly

$3.75M USD

Funder NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
Recipient Organization Rice University
Country United States
Start Date Sep 10, 2024
End Date Jul 31, 2029
Duration 1,785 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10941264
Grant Description

Project Summary / Abstract The ability to visualize specific gene expression, exemplified by methods like green fluorescent protein (GFP) reporters, has been pivotal in scientific research over the past few decades. However, most of these techniques

rely on optics, and are therefore limited by the ~1 mm penetration depth of light into biological tissues. It is in this context that a class of air-filled protein nanostructures named gas vesicles (GVs) were developed as the first acoustic reporter genes, which enabled the use of ultrasound to image gene expression in cells located in

centimeter-deep tissues. Since then, biomolecular engineering of GVs has rapidly expanded the use of these unique air-filled protein nanostructures into directions such as spatially cellular control, drug delivery, pressure sensing, gas delivery, neuromodulation, and multimodal imaging. Despite the rapid progress in the biomedical

applications of GVs, the understanding of the genetics and biophysics underlying GV formation lags behind, and it has been recognized that the assembly of GVs in non-native host organisms is far from optimal compared to that in the native host cells. This gap poses a significant, universal obstacle in almost all GV-based technologies,

strongly hindering their adaptability and application. Our research program aims to address this challenge by pursuing two parallel directions. In the first, we delve into the fundamental science to unravel the molecular mechanism of GV assembly. In the second, we focus on engineering control, using synthetic biology strategies

to design genetic constructs that achieve optimal GV assembly. If successful, the discoveries from these projects will not only enhance our fundamental understanding of this intriguing class of protein organelles, but also revolutionize the biomolecular engineering of GVs, which will generate a major impact for all the biomedical

applications of this class of nanostructures in molecular imaging, cellular control, theranostic nano-agents, and biosensing.

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Rice University

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