4.8 Article

Rapid and Sensitive Detection of Antigen from SARS-CoV-2 Variants of Concern by a Multivalent Minibinder-Functionalized Nanomechanical Sensor

Journal

ANALYTICAL CHEMISTRY
Volume 94, Issue 23, Pages 8105-8109

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.2c01221

Keywords

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Funding

  1. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource [NSF-ECCS-1542205]
  2. MRSEC Program at the Materials Research Center [NSF DMR-1121262]
  3. International Institute for Nanotechnology (IIN)
  4. Keck Foundation
  5. State of Illinois, through the IIN
  6. National Heart, Lung and Blood Institute [1400-SUB/3U54HL119810-07S1]
  7. National Defense Science and Engineering Graduate (NDSEG) Fellowship Program [NDSEG-36373]
  8. Packard Foundation
  9. Defense Threat Reduction Agency [HDTRA-12-01-0004, HDTRA-12-11-0038]
  10. National Science Foundation Rapid [MCB-2028651]
  11. Office of the Provost
  12. Office for Research
  13. Northwestern University Information Technology
  14. Dixon Translational Research Grant by Dixon Family Foundation
  15. Northwestern Center for Advanced Technologies (NUCATS)
  16. CTSA supplement [NCATS UL1 TR002389]
  17. Northwestern University Cancer Center [P30 CA060553]
  18. NIH [U19 AI135964, P30 AI117943, R21 AI163912]
  19. Walder Foundation Foundation's Chicago Coronavirus Assessment Network (Chicago CAN) Initiative

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This study reports the development of a nanomechanical sensor-based platform for rapid and sensitive detection of SARS-CoV-2 variants. The sensor utilizes computationally designed multivalent minibinders immobilized on a microcantilever surface, demonstrating high sensitivity and rapid detection. Clinical validation of the sensor shows detection of antigens from the Omicron (BA-1) variant.
New platforms for the rapid and sensitive detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern are urgently needed. Here we report the development of a nanomechanical sensor based on the deflection of a microcantilever capable of detecting the SARS-CoV-2 spike (S) glycoprotein antigen using computationally designed multivalent minibinders immobilized on a microcantilever surface. The sensor exhibits rapid (<5 min) detection of the target antigens down to concentrations of 0.05 ng/mL (362 fM) and is more than an order of magnitude more sensitive than an antibody-based cantilever sensor. Validation of the sensor with clinical samples from 33 patients, including 9 patients infected with the Omicron (BA-1) variant observed detection of antigen from nasopharyngeal swabs with cycle threshold (Ct) values as high as 39, suggesting a limit of detection similar to that of the quantitative reverse transcription polymerase chain reaction (RT-qPCR). Our findings demonstrate the use of minibinders and nanomechanical sensors for the rapid and sensitive detection of SARS-CoV-2 and potentially other disease markers.

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