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A Dual-Channel Microfluidic Chip for Single Tobacco Protoplast Isolation and Dynamic Capture
Protoplasts are widely used in gene function verification, subcellular localization, and single-cell sequencing because of their complete physiological activities. The traditional methods based on tissues and organs cannot satisfy the requirement. Therefore, the isolation and capture of a single pro...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787963/ https://www.ncbi.nlm.nih.gov/pubmed/36557407 http://dx.doi.org/10.3390/mi13122109 |
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author | Zhang, Huali Geng, Qianqian Sun, Zhanghua Zhong, Xiaoxiang Yang, Ying Zhang, Shuangyu Li, Ying Zhang, Yali Sun, Lijun |
author_facet | Zhang, Huali Geng, Qianqian Sun, Zhanghua Zhong, Xiaoxiang Yang, Ying Zhang, Shuangyu Li, Ying Zhang, Yali Sun, Lijun |
author_sort | Zhang, Huali |
collection | PubMed |
description | Protoplasts are widely used in gene function verification, subcellular localization, and single-cell sequencing because of their complete physiological activities. The traditional methods based on tissues and organs cannot satisfy the requirement. Therefore, the isolation and capture of a single protoplast are most important to these studies. In this study, a dual-channel microfluidic chip based on PDMS with multi-capture cavities was designed. The design theory of the dual-channel microfluidic chip’s geometry was discussed. The capture mechanism of the single cell in a dual-channel microfluidic chip was studied by simulation analysis. Our results showed that a single polystyrene microsphere or tobacco protoplast was successfully isolated and trapped in this chip. The capture efficiency of the chip was 83.33% for the single tobacco protoplast when the inlet flow rate was 0.75 μL/min. In addition, the dynamic capture of the polystyrene microsphere and tobacco protoplasts was also presented. Overall, our study not only provided a new strategy for the subsequent high throughput single protoplast research, but also laid a theoretical foundation for the capture mechanism of the single cell. |
format | Online Article Text |
id | pubmed-9787963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97879632022-12-24 A Dual-Channel Microfluidic Chip for Single Tobacco Protoplast Isolation and Dynamic Capture Zhang, Huali Geng, Qianqian Sun, Zhanghua Zhong, Xiaoxiang Yang, Ying Zhang, Shuangyu Li, Ying Zhang, Yali Sun, Lijun Micromachines (Basel) Article Protoplasts are widely used in gene function verification, subcellular localization, and single-cell sequencing because of their complete physiological activities. The traditional methods based on tissues and organs cannot satisfy the requirement. Therefore, the isolation and capture of a single protoplast are most important to these studies. In this study, a dual-channel microfluidic chip based on PDMS with multi-capture cavities was designed. The design theory of the dual-channel microfluidic chip’s geometry was discussed. The capture mechanism of the single cell in a dual-channel microfluidic chip was studied by simulation analysis. Our results showed that a single polystyrene microsphere or tobacco protoplast was successfully isolated and trapped in this chip. The capture efficiency of the chip was 83.33% for the single tobacco protoplast when the inlet flow rate was 0.75 μL/min. In addition, the dynamic capture of the polystyrene microsphere and tobacco protoplasts was also presented. Overall, our study not only provided a new strategy for the subsequent high throughput single protoplast research, but also laid a theoretical foundation for the capture mechanism of the single cell. MDPI 2022-11-29 /pmc/articles/PMC9787963/ /pubmed/36557407 http://dx.doi.org/10.3390/mi13122109 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhang, Huali Geng, Qianqian Sun, Zhanghua Zhong, Xiaoxiang Yang, Ying Zhang, Shuangyu Li, Ying Zhang, Yali Sun, Lijun A Dual-Channel Microfluidic Chip for Single Tobacco Protoplast Isolation and Dynamic Capture |
title | A Dual-Channel Microfluidic Chip for Single Tobacco Protoplast Isolation and Dynamic Capture |
title_full | A Dual-Channel Microfluidic Chip for Single Tobacco Protoplast Isolation and Dynamic Capture |
title_fullStr | A Dual-Channel Microfluidic Chip for Single Tobacco Protoplast Isolation and Dynamic Capture |
title_full_unstemmed | A Dual-Channel Microfluidic Chip for Single Tobacco Protoplast Isolation and Dynamic Capture |
title_short | A Dual-Channel Microfluidic Chip for Single Tobacco Protoplast Isolation and Dynamic Capture |
title_sort | dual-channel microfluidic chip for single tobacco protoplast isolation and dynamic capture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787963/ https://www.ncbi.nlm.nih.gov/pubmed/36557407 http://dx.doi.org/10.3390/mi13122109 |
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