TY - JOUR
T1 - Acoustic biosensors for ultrasound imaging of enzyme activity
AU - Lakshmanan, Anupama
AU - Jin, Zhiyang
AU - Nety, Suchita P.
AU - Sawyer, Daniel P.
AU - Lee-Gosselin, Audrey
AU - Malounda, Dina
AU - Swift, Mararet B.
AU - Maresca, David
AU - Shapiro, Mikhail G.
PY - 2020
Y1 - 2020
N2 - Visualizing biomolecular and cellular processes inside intact living organisms is a major goal of chemical biology. However, existing molecular biosensors, based primarily on fluorescent emission, have limited utility in this context due to the scattering of light by tissue. In contrast, ultrasound can easily image deep tissue with high spatiotemporal resolution, but lacks the biosensors needed to connect its contrast to the activity of specific biomolecules such as enzymes. To overcome this limitation, we introduce the first genetically encodable acoustic biosensors—molecules that ‘light up’ in ultrasound imaging in response to protease activity. These biosensors are based on a unique class of air-filled protein nanostructures called gas vesicles, which we engineered to produce nonlinear ultrasound signals in response to the activity of three different protease enzymes. We demonstrate the ability of these biosensors to be imaged in vitro, inside engineered probiotic bacteria, and in vivo in the mouse gastrointestinal tract. [Figure not available: see fulltext.].
AB - Visualizing biomolecular and cellular processes inside intact living organisms is a major goal of chemical biology. However, existing molecular biosensors, based primarily on fluorescent emission, have limited utility in this context due to the scattering of light by tissue. In contrast, ultrasound can easily image deep tissue with high spatiotemporal resolution, but lacks the biosensors needed to connect its contrast to the activity of specific biomolecules such as enzymes. To overcome this limitation, we introduce the first genetically encodable acoustic biosensors—molecules that ‘light up’ in ultrasound imaging in response to protease activity. These biosensors are based on a unique class of air-filled protein nanostructures called gas vesicles, which we engineered to produce nonlinear ultrasound signals in response to the activity of three different protease enzymes. We demonstrate the ability of these biosensors to be imaged in vitro, inside engineered probiotic bacteria, and in vivo in the mouse gastrointestinal tract. [Figure not available: see fulltext.].
UR - http://www.scopus.com/inward/record.url?scp=85087825887&partnerID=8YFLogxK
U2 - 10.1038/s41589-020-0591-0
DO - 10.1038/s41589-020-0591-0
M3 - Article
C2 - 32661379
AN - SCOPUS:85087825887
SN - 1552-4450
VL - 16
SP - 988
EP - 996
JO - Nature Chemical Biology
JF - Nature Chemical Biology
IS - 9
ER -