A Generalizable Fluorescence Sensor Platform for Sample Preparation‐Free Protein Detection

H Helen D. Wu (Department of Radiology Stanford University Stanford CA 94305 USA) T Tuan Trinh (Department of Radiology Stanford University Stanford California USA) T Tongtong Li (Energy Materials and Surface Sciences Unit (EMSSU), Okinawa Institute of Science and Technology Graduate University (OIST), 1919-1 Tancha, Onna-son, Kunigami-gun, Okinawa 904-0495, Japan) S Subhadra Thapa (Department of Medicinal Chemistry and Molecular Pharmacology Purdue University West Lafayette IN 47907 USA) R Robert B. Lee (Department of Bioengineering Stanford University Stanford CA 94305 USA) T Thuy‐Tien Thi Nguyen (Sarafan Chem‐H Stanford University Stanford CA 94305 USA) C Camille F. Petrakian (Department of Chemistry Stanford University Stanford CA 94305 USA) M Michael Eisenstein S Severin T. Schneebeli J Jianing Li (BLSA-ZJU Research Center and Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, China.) H H. Tom Soh (Department of Radiology Stanford University Stanford CA 94305 USA)

Abstract

Abstract Modern molecular detection assays such as enzyme‐linked immunosorbent assays (ELISAs) offer excellent sensitivity and specificity, but typically require multiple reagents and extensive sample preparation, limiting their usefulness as rapid diagnostics. A generalizable biosensor platform is introduced that enables single‐step, sample preparation‐free detection of protein analytes with high sensitivity in complex samples. The NanoFluor system employs Janelia Fluor dyes coupled to a nanobody via HaloTag conjugation with a flexible glycine‐serine linker, where the dye undergoes a switch from a non‐fluorescent to a fluorescent state when the coupled nanobody binds to its target. It is demonstrated that the NanoFluor design achieves detection limits as low as picomolar concentrations across diverse protein targets. Molecular dynamics simulations, coupled with quantum mechanics/molecular mechanics computational models, reveal the mechanistic basis for the fluorescence change, and demonstrate the feasibility of multiplexed detection in complex samples including undiluted serum. This versatile, simple biosensor design can prove valuable for point‐of‐care diagnostics and other molecular detection applications.

Article Details

Volume / Issue Vol. 37, Issue 44
Published November 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (11)

H

Helen D. Wu

Department of Radiology Stanford University Stanford CA 94305 USA

T

Tuan Trinh

Department of Radiology Stanford University Stanford California USA

T

Tongtong Li

Energy Materials and Surface Sciences Unit (EMSSU), Okinawa Institute of Science and Technology Graduate University (OIST), 1919-1 Tancha, Onna-son, Kunigami-gun, Okinawa 904-0495, Japan

S

Subhadra Thapa

Department of Medicinal Chemistry and Molecular Pharmacology Purdue University West Lafayette IN 47907 USA

R

Robert B. Lee

Department of Bioengineering Stanford University Stanford CA 94305 USA

T

Thuy‐Tien Thi Nguyen

Sarafan Chem‐H Stanford University Stanford CA 94305 USA

C

Camille F. Petrakian

Department of Chemistry Stanford University Stanford CA 94305 USA

M

Michael Eisenstein

S

Severin T. Schneebeli

J

Jianing Li

BLSA-ZJU Research Center and Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, China.

H

H. Tom Soh

Department of Radiology Stanford University Stanford CA 94305 USA