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Robust Surface Plasmon Resonance Chips for Repetitive and Accurate Analysis of Lignin–Peptide Interactions
[Image: see text] We have developed novel surface plasmon resonance (SPR) sensor chips whose surfaces bear newly synthesized functional self-assembled monolayer (SAM) anchoring lignin through covalent chemical bonds. The SPR sensor chips are remarkably robust and suitable for repetitive and accurate...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644341/ https://www.ncbi.nlm.nih.gov/pubmed/31458905 http://dx.doi.org/10.1021/acsomega.8b01161 |
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author | Isozaki, Katsuhiro Shimoaka, Takafumi Oshiro, Satoshi Yamaguchi, Asako Pincella, Francesca Ueno, Ryo Hasegawa, Takeshi Watanabe, Takashi Takaya, Hikaru Nakamura, Masaharu |
author_facet | Isozaki, Katsuhiro Shimoaka, Takafumi Oshiro, Satoshi Yamaguchi, Asako Pincella, Francesca Ueno, Ryo Hasegawa, Takeshi Watanabe, Takashi Takaya, Hikaru Nakamura, Masaharu |
author_sort | Isozaki, Katsuhiro |
collection | PubMed |
description | [Image: see text] We have developed novel surface plasmon resonance (SPR) sensor chips whose surfaces bear newly synthesized functional self-assembled monolayer (SAM) anchoring lignin through covalent chemical bonds. The SPR sensor chips are remarkably robust and suitable for repetitive and accurate measurement of noncovalent lignin–peptide interactions, which is of significant interest in the chemical or biochemical conversion of renewable woody biomass to valuable chemical feedstocks. The lignin-anchored SAMs were prepared for the first time by click chemistry based on an azide–alkyne Huisgen cycloaddition: mixed SAMs are fabricated on gold thin film using a mixture of alkynyl and methyl thioalkyloligo(ethylene oxide) disulfides and then reacted with azidated milled wood lignins to furnish the functional SAMs anchoring lignins covalently. The resulting SAMs were characterized using infrared reflection–absorption, Raman, and X-ray photoelectron spectroscopies to confirm covalent immobilization of the lignins to the SAMs via triazole linkages and also to reveal that the SAM formation induces a helical conformation of the ethylene oxide chains. Further, SPR measurements of the noncovalent lignin–peptide interactions using lignin-binding peptides have demonstrated high reproducibility and durability of the prepared lignin-anchored sensor chips. |
format | Online Article Text |
id | pubmed-6644341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66443412019-08-27 Robust Surface Plasmon Resonance Chips for Repetitive and Accurate Analysis of Lignin–Peptide Interactions Isozaki, Katsuhiro Shimoaka, Takafumi Oshiro, Satoshi Yamaguchi, Asako Pincella, Francesca Ueno, Ryo Hasegawa, Takeshi Watanabe, Takashi Takaya, Hikaru Nakamura, Masaharu ACS Omega [Image: see text] We have developed novel surface plasmon resonance (SPR) sensor chips whose surfaces bear newly synthesized functional self-assembled monolayer (SAM) anchoring lignin through covalent chemical bonds. The SPR sensor chips are remarkably robust and suitable for repetitive and accurate measurement of noncovalent lignin–peptide interactions, which is of significant interest in the chemical or biochemical conversion of renewable woody biomass to valuable chemical feedstocks. The lignin-anchored SAMs were prepared for the first time by click chemistry based on an azide–alkyne Huisgen cycloaddition: mixed SAMs are fabricated on gold thin film using a mixture of alkynyl and methyl thioalkyloligo(ethylene oxide) disulfides and then reacted with azidated milled wood lignins to furnish the functional SAMs anchoring lignins covalently. The resulting SAMs were characterized using infrared reflection–absorption, Raman, and X-ray photoelectron spectroscopies to confirm covalent immobilization of the lignins to the SAMs via triazole linkages and also to reveal that the SAM formation induces a helical conformation of the ethylene oxide chains. Further, SPR measurements of the noncovalent lignin–peptide interactions using lignin-binding peptides have demonstrated high reproducibility and durability of the prepared lignin-anchored sensor chips. American Chemical Society 2018-07-09 /pmc/articles/PMC6644341/ /pubmed/31458905 http://dx.doi.org/10.1021/acsomega.8b01161 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Isozaki, Katsuhiro Shimoaka, Takafumi Oshiro, Satoshi Yamaguchi, Asako Pincella, Francesca Ueno, Ryo Hasegawa, Takeshi Watanabe, Takashi Takaya, Hikaru Nakamura, Masaharu Robust Surface Plasmon Resonance Chips for Repetitive and Accurate Analysis of Lignin–Peptide Interactions |
title | Robust Surface Plasmon Resonance Chips for Repetitive
and Accurate Analysis of Lignin–Peptide Interactions |
title_full | Robust Surface Plasmon Resonance Chips for Repetitive
and Accurate Analysis of Lignin–Peptide Interactions |
title_fullStr | Robust Surface Plasmon Resonance Chips for Repetitive
and Accurate Analysis of Lignin–Peptide Interactions |
title_full_unstemmed | Robust Surface Plasmon Resonance Chips for Repetitive
and Accurate Analysis of Lignin–Peptide Interactions |
title_short | Robust Surface Plasmon Resonance Chips for Repetitive
and Accurate Analysis of Lignin–Peptide Interactions |
title_sort | robust surface plasmon resonance chips for repetitive
and accurate analysis of lignin–peptide interactions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644341/ https://www.ncbi.nlm.nih.gov/pubmed/31458905 http://dx.doi.org/10.1021/acsomega.8b01161 |
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