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Low Surface Potential with Glycoconjugates Determines Insect Cell Adhesion at Room Temperature
[Image: see text] Cell-coupled field-effect transistor (FET) biosensors have attracted considerable attention because of their high sensitivity to biomolecules. The use of insect cells (Sf21) as a core sensor element is advantageous due to their stable adhesion to sensors at room temperature. Althou...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575668/ https://www.ncbi.nlm.nih.gov/pubmed/36201238 http://dx.doi.org/10.1021/acs.jpclett.2c01673 |
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author | Matsuzaki, Takahisa Terutsuki, Daigo Sato, Shoma Ikarashi, Kohei Sato, Kohei Mitsuno, Hidefumi Okumura, Ryu Yoshimura, Yudai Usami, Shigeyoshi Mori, Yusuke Fujii, Mai Takemi, Shota Nakabayashi, Seiichiro Yoshikawa, Hiroshi Y. Kanzaki, Ryohei |
author_facet | Matsuzaki, Takahisa Terutsuki, Daigo Sato, Shoma Ikarashi, Kohei Sato, Kohei Mitsuno, Hidefumi Okumura, Ryu Yoshimura, Yudai Usami, Shigeyoshi Mori, Yusuke Fujii, Mai Takemi, Shota Nakabayashi, Seiichiro Yoshikawa, Hiroshi Y. Kanzaki, Ryohei |
author_sort | Matsuzaki, Takahisa |
collection | PubMed |
description | [Image: see text] Cell-coupled field-effect transistor (FET) biosensors have attracted considerable attention because of their high sensitivity to biomolecules. The use of insect cells (Sf21) as a core sensor element is advantageous due to their stable adhesion to sensors at room temperature. Although visualization of the insect cell–substrate interface leads to logical amplification of signals, the spatiotemporal processes at the interfaces have not yet been elucidated. We quantitatively monitored the adhesion dynamics of Sf21 using interference reflection microscopy (IRM). Specific adhesion signatures with ring-like patches along the cellular periphery were detected. A combination of zeta potential measurements and lectin staining identified specific glycoconjugates with low electrostatic potentials. The ring-like structures were disrupted after cholesterol depletion, suggesting a raft domain along the cell periphery. Our results indicate dynamic and asymmetric cell adhesion is due to low electrostatic repulsion with fluidic sugar rafts. We envision the logical design of cell–sensor interfaces with an electrical model that accounts for actual adhesion interfaces. |
format | Online Article Text |
id | pubmed-9575668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95756682023-10-06 Low Surface Potential with Glycoconjugates Determines Insect Cell Adhesion at Room Temperature Matsuzaki, Takahisa Terutsuki, Daigo Sato, Shoma Ikarashi, Kohei Sato, Kohei Mitsuno, Hidefumi Okumura, Ryu Yoshimura, Yudai Usami, Shigeyoshi Mori, Yusuke Fujii, Mai Takemi, Shota Nakabayashi, Seiichiro Yoshikawa, Hiroshi Y. Kanzaki, Ryohei J Phys Chem Lett [Image: see text] Cell-coupled field-effect transistor (FET) biosensors have attracted considerable attention because of their high sensitivity to biomolecules. The use of insect cells (Sf21) as a core sensor element is advantageous due to their stable adhesion to sensors at room temperature. Although visualization of the insect cell–substrate interface leads to logical amplification of signals, the spatiotemporal processes at the interfaces have not yet been elucidated. We quantitatively monitored the adhesion dynamics of Sf21 using interference reflection microscopy (IRM). Specific adhesion signatures with ring-like patches along the cellular periphery were detected. A combination of zeta potential measurements and lectin staining identified specific glycoconjugates with low electrostatic potentials. The ring-like structures were disrupted after cholesterol depletion, suggesting a raft domain along the cell periphery. Our results indicate dynamic and asymmetric cell adhesion is due to low electrostatic repulsion with fluidic sugar rafts. We envision the logical design of cell–sensor interfaces with an electrical model that accounts for actual adhesion interfaces. American Chemical Society 2022-10-06 2022-10-13 /pmc/articles/PMC9575668/ /pubmed/36201238 http://dx.doi.org/10.1021/acs.jpclett.2c01673 Text en © 2022 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Matsuzaki, Takahisa Terutsuki, Daigo Sato, Shoma Ikarashi, Kohei Sato, Kohei Mitsuno, Hidefumi Okumura, Ryu Yoshimura, Yudai Usami, Shigeyoshi Mori, Yusuke Fujii, Mai Takemi, Shota Nakabayashi, Seiichiro Yoshikawa, Hiroshi Y. Kanzaki, Ryohei Low Surface Potential with Glycoconjugates Determines Insect Cell Adhesion at Room Temperature |
title | Low Surface
Potential with Glycoconjugates Determines
Insect Cell Adhesion at Room Temperature |
title_full | Low Surface
Potential with Glycoconjugates Determines
Insect Cell Adhesion at Room Temperature |
title_fullStr | Low Surface
Potential with Glycoconjugates Determines
Insect Cell Adhesion at Room Temperature |
title_full_unstemmed | Low Surface
Potential with Glycoconjugates Determines
Insect Cell Adhesion at Room Temperature |
title_short | Low Surface
Potential with Glycoconjugates Determines
Insect Cell Adhesion at Room Temperature |
title_sort | low surface
potential with glycoconjugates determines
insect cell adhesion at room temperature |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575668/ https://www.ncbi.nlm.nih.gov/pubmed/36201238 http://dx.doi.org/10.1021/acs.jpclett.2c01673 |
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