| Literature DB >> 32100994 |
Julia A Kudryashev1, Lauren E Waggoner2, Hope T Leng1, Nicholas H Mininni1, Ester J Kwon1.
Abstract
Currently, traumatic brain injury (TBI) is detected by medical imaging; however, medical imaging requires expensive capital equipment, is time- and resource-intensive, and is poor at predicting patient prognosis. To date, direct measurement of elevated protease activity has yet to be utilized to detect TBI. In this work, we engineered an activity-based nanosensor for TBI (TBI-ABN) that responds to increased protease activity initiated after brain injury. We establish that a calcium-sensitive protease, calpain-1, is active in the injured brain hours within injury. We then optimize the molecular weight of a nanoscale polymeric carrier to infiltrate into the injured brain tissue with minimal renal filtration. A calpain-1 substrate that generates a fluorescent signal upon cleavage was attached to this nanoscale polymeric carrier to generate an engineered TBI-ABN. When applied intravenously to a mouse model of TBI, our engineered sensor is observed to locally activate in the injured brain tissue. This TBI-ABN is the first demonstration of a sensor that responds to protease activity to detect TBI.Entities:
Keywords: activity-based nanosensor; calpain-1; nanomedicine; protease activity; traumatic brain injury
Mesh:
Substances:
Year: 2020 PMID: 32100994 PMCID: PMC7534893 DOI: 10.1021/acssensors.9b01812
Source DB: PubMed Journal: ACS Sens ISSN: 2379-3694 Impact factor: 7.711