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Liquid crystal-amplified optofluidic biosensor for ultra-highly sensitive and stable protein assay
Protein assays show great importance in medical research and disease diagnoses. Liquid crystals (LCs), as a branch of sensitive materials, offer promising applicability in the field of biosensing. Herein, we developed an ultrasensitive biosensor for the detection of low-concentration protein molecul...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397869/ https://www.ncbi.nlm.nih.gov/pubmed/34806024 http://dx.doi.org/10.1186/s43074-021-00041-1 |
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author | Wang, Ziyihui Liu, Yize Gong, Chaoyang Yuan, Zhiyi Shen, Liang Chang, Pengxiang Liu, Kun Xu, Tianhua Jiang, Junfeng Chen, Yu-Cheng Liu, Tiegen |
author_facet | Wang, Ziyihui Liu, Yize Gong, Chaoyang Yuan, Zhiyi Shen, Liang Chang, Pengxiang Liu, Kun Xu, Tianhua Jiang, Junfeng Chen, Yu-Cheng Liu, Tiegen |
author_sort | Wang, Ziyihui |
collection | PubMed |
description | Protein assays show great importance in medical research and disease diagnoses. Liquid crystals (LCs), as a branch of sensitive materials, offer promising applicability in the field of biosensing. Herein, we developed an ultrasensitive biosensor for the detection of low-concentration protein molecules, employing LC-amplified optofluidic resonators. In this design, the orientation of LCs was disturbed by immobilized protein molecules through the reduction of the vertical anchoring force from the alignment layer. A biosensing platform based on the whispering-gallery mode (WGM) from the LC-amplified optofluidic resonator was developed and explored, in which the spectral wavelength shift was monitored as the sensing parameter. The microbubble structure provided a stable and reliable WGM resonator with a high Q factor for LCs. It is demonstrated that the wall thickness of the microbubble played a key role in enhancing the sensitivity of the LC-amplified WGM microcavity. It is also found that protein molecules coated on the internal surface of microbubble led to their interactions with laser beams and the orientation transition of LCs. Both effects amplified the target information and triggered a sensitive wavelength shift in WGM spectra. A detection limit of 1 fM for bovine serum albumin (BSA) was achieved to demonstrate the high-sensitivity of our sensing platform in protein assays. Compared to the detection using a conventional polarized optical microscope (POM), the sensitivity was improved by seven orders of magnitude. Furthermore, multiple types of proteins and specific biosensing were also investigated to verify the potential of LC-amplified optofluidic resonators in the biomolecular detection. Our studies indicate that LC-amplified optofluidic resonators offer a new solution for the ultrasensitive real-time biosensing and the characterization of biomolecular interactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s43074-021-00041-1. |
format | Online Article Text |
id | pubmed-8397869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-83978692021-08-30 Liquid crystal-amplified optofluidic biosensor for ultra-highly sensitive and stable protein assay Wang, Ziyihui Liu, Yize Gong, Chaoyang Yuan, Zhiyi Shen, Liang Chang, Pengxiang Liu, Kun Xu, Tianhua Jiang, Junfeng Chen, Yu-Cheng Liu, Tiegen PhotoniX Research Protein assays show great importance in medical research and disease diagnoses. Liquid crystals (LCs), as a branch of sensitive materials, offer promising applicability in the field of biosensing. Herein, we developed an ultrasensitive biosensor for the detection of low-concentration protein molecules, employing LC-amplified optofluidic resonators. In this design, the orientation of LCs was disturbed by immobilized protein molecules through the reduction of the vertical anchoring force from the alignment layer. A biosensing platform based on the whispering-gallery mode (WGM) from the LC-amplified optofluidic resonator was developed and explored, in which the spectral wavelength shift was monitored as the sensing parameter. The microbubble structure provided a stable and reliable WGM resonator with a high Q factor for LCs. It is demonstrated that the wall thickness of the microbubble played a key role in enhancing the sensitivity of the LC-amplified WGM microcavity. It is also found that protein molecules coated on the internal surface of microbubble led to their interactions with laser beams and the orientation transition of LCs. Both effects amplified the target information and triggered a sensitive wavelength shift in WGM spectra. A detection limit of 1 fM for bovine serum albumin (BSA) was achieved to demonstrate the high-sensitivity of our sensing platform in protein assays. Compared to the detection using a conventional polarized optical microscope (POM), the sensitivity was improved by seven orders of magnitude. Furthermore, multiple types of proteins and specific biosensing were also investigated to verify the potential of LC-amplified optofluidic resonators in the biomolecular detection. Our studies indicate that LC-amplified optofluidic resonators offer a new solution for the ultrasensitive real-time biosensing and the characterization of biomolecular interactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s43074-021-00041-1. Springer Singapore 2021-08-28 2021 /pmc/articles/PMC8397869/ /pubmed/34806024 http://dx.doi.org/10.1186/s43074-021-00041-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Wang, Ziyihui Liu, Yize Gong, Chaoyang Yuan, Zhiyi Shen, Liang Chang, Pengxiang Liu, Kun Xu, Tianhua Jiang, Junfeng Chen, Yu-Cheng Liu, Tiegen Liquid crystal-amplified optofluidic biosensor for ultra-highly sensitive and stable protein assay |
title | Liquid crystal-amplified optofluidic biosensor for ultra-highly sensitive and stable protein assay |
title_full | Liquid crystal-amplified optofluidic biosensor for ultra-highly sensitive and stable protein assay |
title_fullStr | Liquid crystal-amplified optofluidic biosensor for ultra-highly sensitive and stable protein assay |
title_full_unstemmed | Liquid crystal-amplified optofluidic biosensor for ultra-highly sensitive and stable protein assay |
title_short | Liquid crystal-amplified optofluidic biosensor for ultra-highly sensitive and stable protein assay |
title_sort | liquid crystal-amplified optofluidic biosensor for ultra-highly sensitive and stable protein assay |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397869/ https://www.ncbi.nlm.nih.gov/pubmed/34806024 http://dx.doi.org/10.1186/s43074-021-00041-1 |
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