Sculpting nanoparticle dynamics for single-bacteria-level screening and direct binding-efficiency measurement

Particle trapping and binding in optical potential wells provide a versatile platform for various biomedical applications. However, implementation systems to study multi-particle contact interactions in an optical lattice remain rare. By configuring an optofluidic lattice, we demonstrate the precise...

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Bibliographic Details
Main Authors: Shi, Yu Zhi, Xiong, Sha, Zhang, Yi, Chin, Lip Ket, Chen, Yan-Yu, Zhang, Jing Bo, Ser, Wee, Hoi, Lim Siau, Liedberg, Bo, Yap, Peng Huat, Tsai, Din Ping, Liu, Ai Qun, Zhang, T. H., Larson, A., Wu, J. H., Chen, T. N., Yang, Z. C., Hao, Y. L., Qiu, C.-W.
Other Authors: School of Electrical and Electronic Engineering
Format: Article
Language:English
Published: 2018
Subjects:
Online Access:https://hdl.handle.net/10356/87504
http://hdl.handle.net/10220/45434
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Institution: Nanyang Technological University
Language: English
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Summary:Particle trapping and binding in optical potential wells provide a versatile platform for various biomedical applications. However, implementation systems to study multi-particle contact interactions in an optical lattice remain rare. By configuring an optofluidic lattice, we demonstrate the precise control of particle interactions and functions such as controlling aggregation and multi-hopping. The mean residence time of a single particle is found considerably reduced from 7 s, as predicted by Kramer’s theory, to 0.6 s, owing to the mechanical interactions among aggregated particles. The optofluidic lattice also enables single-bacteria-level screening of biological binding agents such as antibodies through particle-enabled bacteria hopping. The binding efficiency of antibodies could be determined directly, selectively, quantitatively and efficiently. This work enriches the fundamental mechanisms of particle kinetics and offers new possibilities for probing and utilising unprecedented biomolecule interactions at single-bacteria level.