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Reversible Immunoaffinity Interface Enables Dynamic Manipulation of Trapping Force for Accumulated Capture and Efficient Release of Circulating Rare Cells

Controllable assembly and disassembly of recognition interface are vital for bioanalysis. Herein, a strategy of dynamic manipulation of trapping force by engineering a dynamic and reversible immunoaffinity microinterface (DynarFace) in a herringbone chip (DynarFace‐Chip) for liquid biopsy is propose...

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Autores principales: Chen, Xiaofeng, Ding, Hongming, Zhang, Dongdong, Zhao, Kaifeng, Gao, Jiafeng, Lin, Bingqian, Huang, Chen, Song, Yanling, Zhao, Gang, Ma, Yuqiang, Wu, Lingling, Yang, Chaoyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529431/
https://www.ncbi.nlm.nih.gov/pubmed/34473422
http://dx.doi.org/10.1002/advs.202102070
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author Chen, Xiaofeng
Ding, Hongming
Zhang, Dongdong
Zhao, Kaifeng
Gao, Jiafeng
Lin, Bingqian
Huang, Chen
Song, Yanling
Zhao, Gang
Ma, Yuqiang
Wu, Lingling
Yang, Chaoyong
author_facet Chen, Xiaofeng
Ding, Hongming
Zhang, Dongdong
Zhao, Kaifeng
Gao, Jiafeng
Lin, Bingqian
Huang, Chen
Song, Yanling
Zhao, Gang
Ma, Yuqiang
Wu, Lingling
Yang, Chaoyong
author_sort Chen, Xiaofeng
collection PubMed
description Controllable assembly and disassembly of recognition interface are vital for bioanalysis. Herein, a strategy of dynamic manipulation of trapping force by engineering a dynamic and reversible immunoaffinity microinterface (DynarFace) in a herringbone chip (DynarFace‐Chip) for liquid biopsy is proposed. The DynarFace is assembled by magnetically attracting immunomagnetic beads (IMBs) on chip substrate, with merits of convenient operation and reversible assembly. The DynarFace allows accumulating attachment of IMBs on circulating rare cell (CRC) surfaces during hydrodynamically enhanced interface collision, where accumulatively enhanced magnetic trapping force improves capture efficiency toward CRCs with medium expression of biomarkers from blood samples by 134.81% compared with traditional non‐dynamic interfaces. Moreover, magnet withdrawing‐induced disappearance of trapping force affords DynarFace disassembly and CRC release with high efficiency (>98%) and high viability (≈98%), compatible with downstream in vitro culture and gene analysis of CRCs. This DynarFace strategy opens a new avenue to accumulated capture and reversible release of CRCs, holding great potential for liquid biopsy‐based precision medicine.
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spelling pubmed-85294312021-10-27 Reversible Immunoaffinity Interface Enables Dynamic Manipulation of Trapping Force for Accumulated Capture and Efficient Release of Circulating Rare Cells Chen, Xiaofeng Ding, Hongming Zhang, Dongdong Zhao, Kaifeng Gao, Jiafeng Lin, Bingqian Huang, Chen Song, Yanling Zhao, Gang Ma, Yuqiang Wu, Lingling Yang, Chaoyong Adv Sci (Weinh) Research Articles Controllable assembly and disassembly of recognition interface are vital for bioanalysis. Herein, a strategy of dynamic manipulation of trapping force by engineering a dynamic and reversible immunoaffinity microinterface (DynarFace) in a herringbone chip (DynarFace‐Chip) for liquid biopsy is proposed. The DynarFace is assembled by magnetically attracting immunomagnetic beads (IMBs) on chip substrate, with merits of convenient operation and reversible assembly. The DynarFace allows accumulating attachment of IMBs on circulating rare cell (CRC) surfaces during hydrodynamically enhanced interface collision, where accumulatively enhanced magnetic trapping force improves capture efficiency toward CRCs with medium expression of biomarkers from blood samples by 134.81% compared with traditional non‐dynamic interfaces. Moreover, magnet withdrawing‐induced disappearance of trapping force affords DynarFace disassembly and CRC release with high efficiency (>98%) and high viability (≈98%), compatible with downstream in vitro culture and gene analysis of CRCs. This DynarFace strategy opens a new avenue to accumulated capture and reversible release of CRCs, holding great potential for liquid biopsy‐based precision medicine. John Wiley and Sons Inc. 2021-09-02 /pmc/articles/PMC8529431/ /pubmed/34473422 http://dx.doi.org/10.1002/advs.202102070 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Chen, Xiaofeng
Ding, Hongming
Zhang, Dongdong
Zhao, Kaifeng
Gao, Jiafeng
Lin, Bingqian
Huang, Chen
Song, Yanling
Zhao, Gang
Ma, Yuqiang
Wu, Lingling
Yang, Chaoyong
Reversible Immunoaffinity Interface Enables Dynamic Manipulation of Trapping Force for Accumulated Capture and Efficient Release of Circulating Rare Cells
title Reversible Immunoaffinity Interface Enables Dynamic Manipulation of Trapping Force for Accumulated Capture and Efficient Release of Circulating Rare Cells
title_full Reversible Immunoaffinity Interface Enables Dynamic Manipulation of Trapping Force for Accumulated Capture and Efficient Release of Circulating Rare Cells
title_fullStr Reversible Immunoaffinity Interface Enables Dynamic Manipulation of Trapping Force for Accumulated Capture and Efficient Release of Circulating Rare Cells
title_full_unstemmed Reversible Immunoaffinity Interface Enables Dynamic Manipulation of Trapping Force for Accumulated Capture and Efficient Release of Circulating Rare Cells
title_short Reversible Immunoaffinity Interface Enables Dynamic Manipulation of Trapping Force for Accumulated Capture and Efficient Release of Circulating Rare Cells
title_sort reversible immunoaffinity interface enables dynamic manipulation of trapping force for accumulated capture and efficient release of circulating rare cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529431/
https://www.ncbi.nlm.nih.gov/pubmed/34473422
http://dx.doi.org/10.1002/advs.202102070
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