Loading…

A mixing microfluidic chip for real-time NMR monitoring of macromolecular reactions

Abstract NMR spectroscopy permits real-time monitoring of reactions that involve changes in the spectra of reactants. MICCS (MIcro Channelled Cell for Synthesis monitoring) is a microfluidic chip for such purposes, which is used to rapidly activate reactions by mixing the reactant solutions in the c...

Full description

Saved in:
Bibliographic Details
Published in:Journal of biochemistry (Tokyo) 2021-09, Vol.170 (3), p.363-368
Main Authors: Yamasaki, Kazuhiko, Yamasaki, Tomoko, Takahashi, Masaharu, Suematsu, Hiroto
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c345t-747f8dafd970bc510b42b0db3e077d46009c5864a6b7899dc33c532cf431f2c33
cites cdi_FETCH-LOGICAL-c345t-747f8dafd970bc510b42b0db3e077d46009c5864a6b7899dc33c532cf431f2c33
container_end_page 368
container_issue 3
container_start_page 363
container_title Journal of biochemistry (Tokyo)
container_volume 170
creator Yamasaki, Kazuhiko
Yamasaki, Tomoko
Takahashi, Masaharu
Suematsu, Hiroto
description Abstract NMR spectroscopy permits real-time monitoring of reactions that involve changes in the spectra of reactants. MICCS (MIcro Channelled Cell for Synthesis monitoring) is a microfluidic chip for such purposes, which is used to rapidly activate reactions by mixing the reactant solutions in the chip inserted into the typical NMR tube. Although it allows monitoring of chemical reactions of small compounds, its simple mixing system dependent on diffusion in the microchannel was not suitable for macromolecules such as proteins with low diffusion rates. Here, we developed a new microfluidic chip based on MICCS by incorporating a mixer of split-and-recombination type within the microchannel. We applied it to monitoring of the protein-folding reaction in a stopped-flow mode. A solution of denaturant-unfolded RNase A was injected from a syringe pump into the microchip set inside the NMR magnet and mixed with a buffer for dilution to reach the folding condition. Immediately after dilution, the reaction was initiated and detected by a series of NMR measurements that were synchronized with activation and inactivation of the pump. The process was repeated for accumulation of the data. By analysing the change of the spectra by factor analysis, a kinetic constant of 0.57 min−1 was obtained. Graphical Abstract
doi_str_mv 10.1093/jb/mvab048
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2511241371</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1093/jb/mvab048</oup_id><sourcerecordid>2511241371</sourcerecordid><originalsourceid>FETCH-LOGICAL-c345t-747f8dafd970bc510b42b0db3e077d46009c5864a6b7899dc33c532cf431f2c33</originalsourceid><addsrcrecordid>eNp90MtKxDAUBuAgCo6jG58gG0GEOrm1aZfD4A1GBS_griRpohmSpiat6NvbOrN2dfjhO4fDD8ApRpcYVXSxkQv_JSRi5R6YYZ4XGSlyvA9mCBGcVYS9HYKjlDZTJJTOwPMSevtt2_dxqBiMG2xjFVQftoMmRBi1cFlvvYYP90_Qh9b2IU48GOjFuOGD02pw4o-q3oY2HYMDI1zSJ7s5B6_XVy-r22z9eHO3Wq4zRVneZ5xxUzbCNBVHUuUYSUYkaiTViPOGFQhVKi8LJgrJy6pqFKUqp0QZRrEhY5qD8-3dLobPQae-9jYp7ZxodRhSTXKMCcOU45FebOn4cUpRm7qL1ov4U2NUT83VG1nvmhvx2RaHofvP_QKpDm7v</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2511241371</pqid></control><display><type>article</type><title>A mixing microfluidic chip for real-time NMR monitoring of macromolecular reactions</title><source>Oxford Journals Online</source><creator>Yamasaki, Kazuhiko ; Yamasaki, Tomoko ; Takahashi, Masaharu ; Suematsu, Hiroto</creator><creatorcontrib>Yamasaki, Kazuhiko ; Yamasaki, Tomoko ; Takahashi, Masaharu ; Suematsu, Hiroto</creatorcontrib><description>Abstract NMR spectroscopy permits real-time monitoring of reactions that involve changes in the spectra of reactants. MICCS (MIcro Channelled Cell for Synthesis monitoring) is a microfluidic chip for such purposes, which is used to rapidly activate reactions by mixing the reactant solutions in the chip inserted into the typical NMR tube. Although it allows monitoring of chemical reactions of small compounds, its simple mixing system dependent on diffusion in the microchannel was not suitable for macromolecules such as proteins with low diffusion rates. Here, we developed a new microfluidic chip based on MICCS by incorporating a mixer of split-and-recombination type within the microchannel. We applied it to monitoring of the protein-folding reaction in a stopped-flow mode. A solution of denaturant-unfolded RNase A was injected from a syringe pump into the microchip set inside the NMR magnet and mixed with a buffer for dilution to reach the folding condition. Immediately after dilution, the reaction was initiated and detected by a series of NMR measurements that were synchronized with activation and inactivation of the pump. The process was repeated for accumulation of the data. By analysing the change of the spectra by factor analysis, a kinetic constant of 0.57 min−1 was obtained. Graphical Abstract</description><identifier>ISSN: 0021-924X</identifier><identifier>EISSN: 1756-2651</identifier><identifier>DOI: 10.1093/jb/mvab048</identifier><language>eng</language><publisher>Oxford University Press</publisher><ispartof>Journal of biochemistry (Tokyo), 2021-09, Vol.170 (3), p.363-368</ispartof><rights>The Author(s) 2021. Published by Oxford University Press on behalf of the Japanese Biochemical Society. All rights reserved 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c345t-747f8dafd970bc510b42b0db3e077d46009c5864a6b7899dc33c532cf431f2c33</citedby><cites>FETCH-LOGICAL-c345t-747f8dafd970bc510b42b0db3e077d46009c5864a6b7899dc33c532cf431f2c33</cites><orcidid>0000-0003-0320-9697</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Yamasaki, Kazuhiko</creatorcontrib><creatorcontrib>Yamasaki, Tomoko</creatorcontrib><creatorcontrib>Takahashi, Masaharu</creatorcontrib><creatorcontrib>Suematsu, Hiroto</creatorcontrib><title>A mixing microfluidic chip for real-time NMR monitoring of macromolecular reactions</title><title>Journal of biochemistry (Tokyo)</title><description>Abstract NMR spectroscopy permits real-time monitoring of reactions that involve changes in the spectra of reactants. MICCS (MIcro Channelled Cell for Synthesis monitoring) is a microfluidic chip for such purposes, which is used to rapidly activate reactions by mixing the reactant solutions in the chip inserted into the typical NMR tube. Although it allows monitoring of chemical reactions of small compounds, its simple mixing system dependent on diffusion in the microchannel was not suitable for macromolecules such as proteins with low diffusion rates. Here, we developed a new microfluidic chip based on MICCS by incorporating a mixer of split-and-recombination type within the microchannel. We applied it to monitoring of the protein-folding reaction in a stopped-flow mode. A solution of denaturant-unfolded RNase A was injected from a syringe pump into the microchip set inside the NMR magnet and mixed with a buffer for dilution to reach the folding condition. Immediately after dilution, the reaction was initiated and detected by a series of NMR measurements that were synchronized with activation and inactivation of the pump. The process was repeated for accumulation of the data. By analysing the change of the spectra by factor analysis, a kinetic constant of 0.57 min−1 was obtained. Graphical Abstract</description><issn>0021-924X</issn><issn>1756-2651</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp90MtKxDAUBuAgCo6jG58gG0GEOrm1aZfD4A1GBS_griRpohmSpiat6NvbOrN2dfjhO4fDD8ApRpcYVXSxkQv_JSRi5R6YYZ4XGSlyvA9mCBGcVYS9HYKjlDZTJJTOwPMSevtt2_dxqBiMG2xjFVQftoMmRBi1cFlvvYYP90_Qh9b2IU48GOjFuOGD02pw4o-q3oY2HYMDI1zSJ7s5B6_XVy-r22z9eHO3Wq4zRVneZ5xxUzbCNBVHUuUYSUYkaiTViPOGFQhVKi8LJgrJy6pqFKUqp0QZRrEhY5qD8-3dLobPQae-9jYp7ZxodRhSTXKMCcOU45FebOn4cUpRm7qL1ov4U2NUT83VG1nvmhvx2RaHofvP_QKpDm7v</recordid><startdate>20210901</startdate><enddate>20210901</enddate><creator>Yamasaki, Kazuhiko</creator><creator>Yamasaki, Tomoko</creator><creator>Takahashi, Masaharu</creator><creator>Suematsu, Hiroto</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0320-9697</orcidid></search><sort><creationdate>20210901</creationdate><title>A mixing microfluidic chip for real-time NMR monitoring of macromolecular reactions</title><author>Yamasaki, Kazuhiko ; Yamasaki, Tomoko ; Takahashi, Masaharu ; Suematsu, Hiroto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c345t-747f8dafd970bc510b42b0db3e077d46009c5864a6b7899dc33c532cf431f2c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamasaki, Kazuhiko</creatorcontrib><creatorcontrib>Yamasaki, Tomoko</creatorcontrib><creatorcontrib>Takahashi, Masaharu</creatorcontrib><creatorcontrib>Suematsu, Hiroto</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biochemistry (Tokyo)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamasaki, Kazuhiko</au><au>Yamasaki, Tomoko</au><au>Takahashi, Masaharu</au><au>Suematsu, Hiroto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A mixing microfluidic chip for real-time NMR monitoring of macromolecular reactions</atitle><jtitle>Journal of biochemistry (Tokyo)</jtitle><date>2021-09-01</date><risdate>2021</risdate><volume>170</volume><issue>3</issue><spage>363</spage><epage>368</epage><pages>363-368</pages><issn>0021-924X</issn><eissn>1756-2651</eissn><abstract>Abstract NMR spectroscopy permits real-time monitoring of reactions that involve changes in the spectra of reactants. MICCS (MIcro Channelled Cell for Synthesis monitoring) is a microfluidic chip for such purposes, which is used to rapidly activate reactions by mixing the reactant solutions in the chip inserted into the typical NMR tube. Although it allows monitoring of chemical reactions of small compounds, its simple mixing system dependent on diffusion in the microchannel was not suitable for macromolecules such as proteins with low diffusion rates. Here, we developed a new microfluidic chip based on MICCS by incorporating a mixer of split-and-recombination type within the microchannel. We applied it to monitoring of the protein-folding reaction in a stopped-flow mode. A solution of denaturant-unfolded RNase A was injected from a syringe pump into the microchip set inside the NMR magnet and mixed with a buffer for dilution to reach the folding condition. Immediately after dilution, the reaction was initiated and detected by a series of NMR measurements that were synchronized with activation and inactivation of the pump. The process was repeated for accumulation of the data. By analysing the change of the spectra by factor analysis, a kinetic constant of 0.57 min−1 was obtained. Graphical Abstract</abstract><pub>Oxford University Press</pub><doi>10.1093/jb/mvab048</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-0320-9697</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0021-924X
ispartof Journal of biochemistry (Tokyo), 2021-09, Vol.170 (3), p.363-368
issn 0021-924X
1756-2651
language eng
recordid cdi_proquest_miscellaneous_2511241371
source Oxford Journals Online
title A mixing microfluidic chip for real-time NMR monitoring of macromolecular reactions
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T20%3A44%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20mixing%20microfluidic%20chip%20for%20real-time%20NMR%20monitoring%20of%20macromolecular%20reactions&rft.jtitle=Journal%20of%20biochemistry%20(Tokyo)&rft.au=Yamasaki,%20Kazuhiko&rft.date=2021-09-01&rft.volume=170&rft.issue=3&rft.spage=363&rft.epage=368&rft.pages=363-368&rft.issn=0021-924X&rft.eissn=1756-2651&rft_id=info:doi/10.1093/jb/mvab048&rft_dat=%3Cproquest_cross%3E2511241371%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c345t-747f8dafd970bc510b42b0db3e077d46009c5864a6b7899dc33c532cf431f2c33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2511241371&rft_id=info:pmid/&rft_oup_id=10.1093/jb/mvab048&rfr_iscdi=true