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AFM Study of the Influence of Glycerol Flow on Horseradish Peroxidase near the in/out Linear Sections of a Coil
Flow-based coiled systems, through which a heat transfer fluid (such as glycerol) is pumped, are widely used for thermal stabilization of bioreactors and biosensor cuvettes and cells. Previously, using horseradish peroxidase (HRP) as a model protein, we have demonstrated that the incubation of a pro...
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Published in: | Applied sciences 2021-02, Vol.11 (4), p.1723 |
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description | Flow-based coiled systems, through which a heat transfer fluid (such as glycerol) is pumped, are widely used for thermal stabilization of bioreactors and biosensor cuvettes and cells. Previously, using horseradish peroxidase (HRP) as a model protein, we have demonstrated that the incubation of a protein solution in a flow-based system over coiled pipe with flowing glycerol leads to a change in the adsorption properties of the protein macromolecules. Herein, we have studied the effect of the glycerol flow on the properties of HRP, the solution of which was placed differently: i.e., near either the inflow or the outflow linear sections of the pipe, while the coiled section of the pipe was shielded with a grounded metallic cover. Atomic force microscopy (AFM) has been employed in order to visualize the HRP protein macromolecules adsorbed from its solution onto the mica substrate surface. The quantity of adsorbed protein was estimated based on the AFM data. The enzymatic activity of HRP was estimated by spectrophotometry. We demonstrate that a change in the properties of HRP enzyme was observed after the incubation of its solution near the inflow/outflow linear sections of the pipe with flowing glycerol. Namely, after the incubation of HRP solution near the inflow section, a decrease in the protein adsorption onto mica was observed, but its enzymatic activity remained unchanged in comparison to the control sample. In another case, when the HRP solution was incubated near the outflow section, an increased protein adsorption was observed, while the enzyme exhibited considerably lower activity. |
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Previously, using horseradish peroxidase (HRP) as a model protein, we have demonstrated that the incubation of a protein solution in a flow-based system over coiled pipe with flowing glycerol leads to a change in the adsorption properties of the protein macromolecules. Herein, we have studied the effect of the glycerol flow on the properties of HRP, the solution of which was placed differently: i.e., near either the inflow or the outflow linear sections of the pipe, while the coiled section of the pipe was shielded with a grounded metallic cover. Atomic force microscopy (AFM) has been employed in order to visualize the HRP protein macromolecules adsorbed from its solution onto the mica substrate surface. The quantity of adsorbed protein was estimated based on the AFM data. The enzymatic activity of HRP was estimated by spectrophotometry. We demonstrate that a change in the properties of HRP enzyme was observed after the incubation of its solution near the inflow/outflow linear sections of the pipe with flowing glycerol. Namely, after the incubation of HRP solution near the inflow section, a decrease in the protein adsorption onto mica was observed, but its enzymatic activity remained unchanged in comparison to the control sample. In another case, when the HRP solution was incubated near the outflow section, an increased protein adsorption was observed, while the enzyme exhibited considerably lower activity.</description><identifier>ISSN: 2076-3417</identifier><identifier>EISSN: 2076-3417</identifier><identifier>DOI: 10.3390/app11041723</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Adsorption ; Atomic force microscopy ; Bioreactors ; Biosensors ; Electromagnetic fields ; Electromagnetism ; Enzymatic activity ; Enzymes ; Experiments ; Flow ; Glycerol ; Heat transfer ; Hemodynamics ; Horseradish peroxidase ; Hrp protein ; liquid flow ; Macromolecules ; Outflow ; Peroxidase ; Pipes ; Protein adsorption ; protein aggregation ; Proteins ; Spectrophotometry ; Structure-function relationships ; triboelectric effect</subject><ispartof>Applied sciences, 2021-02, Vol.11 (4), p.1723</ispartof><rights>2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c364t-3401e4d64eebc8133bc25b7fc8a8dd42159a0751a39671e45f9529d0499e23c13</citedby><cites>FETCH-LOGICAL-c364t-3401e4d64eebc8133bc25b7fc8a8dd42159a0751a39671e45f9529d0499e23c13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2534617856/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2534617856?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,25731,27901,27902,36989,44566,74869</link.rule.ids></links><search><creatorcontrib>Ivanov, Yuri D.</creatorcontrib><creatorcontrib>Pleshakova, Tatyana O.</creatorcontrib><creatorcontrib>Shumov, Ivan D.</creatorcontrib><creatorcontrib>Kozlov, Andrey F.</creatorcontrib><creatorcontrib>Ivanova, Irina A.</creatorcontrib><creatorcontrib>Ershova, Maria O.</creatorcontrib><creatorcontrib>Tatur, Vadim Yu</creatorcontrib><creatorcontrib>Ziborov, Vadim S.</creatorcontrib><title>AFM Study of the Influence of Glycerol Flow on Horseradish Peroxidase near the in/out Linear Sections of a Coil</title><title>Applied sciences</title><description>Flow-based coiled systems, through which a heat transfer fluid (such as glycerol) is pumped, are widely used for thermal stabilization of bioreactors and biosensor cuvettes and cells. Previously, using horseradish peroxidase (HRP) as a model protein, we have demonstrated that the incubation of a protein solution in a flow-based system over coiled pipe with flowing glycerol leads to a change in the adsorption properties of the protein macromolecules. Herein, we have studied the effect of the glycerol flow on the properties of HRP, the solution of which was placed differently: i.e., near either the inflow or the outflow linear sections of the pipe, while the coiled section of the pipe was shielded with a grounded metallic cover. Atomic force microscopy (AFM) has been employed in order to visualize the HRP protein macromolecules adsorbed from its solution onto the mica substrate surface. The quantity of adsorbed protein was estimated based on the AFM data. The enzymatic activity of HRP was estimated by spectrophotometry. We demonstrate that a change in the properties of HRP enzyme was observed after the incubation of its solution near the inflow/outflow linear sections of the pipe with flowing glycerol. Namely, after the incubation of HRP solution near the inflow section, a decrease in the protein adsorption onto mica was observed, but its enzymatic activity remained unchanged in comparison to the control sample. In another case, when the HRP solution was incubated near the outflow section, an increased protein adsorption was observed, while the enzyme exhibited considerably lower activity.</description><subject>Adsorption</subject><subject>Atomic force microscopy</subject><subject>Bioreactors</subject><subject>Biosensors</subject><subject>Electromagnetic fields</subject><subject>Electromagnetism</subject><subject>Enzymatic activity</subject><subject>Enzymes</subject><subject>Experiments</subject><subject>Flow</subject><subject>Glycerol</subject><subject>Heat transfer</subject><subject>Hemodynamics</subject><subject>Horseradish peroxidase</subject><subject>Hrp protein</subject><subject>liquid flow</subject><subject>Macromolecules</subject><subject>Outflow</subject><subject>Peroxidase</subject><subject>Pipes</subject><subject>Protein adsorption</subject><subject>protein aggregation</subject><subject>Proteins</subject><subject>Spectrophotometry</subject><subject>Structure-function relationships</subject><subject>triboelectric effect</subject><issn>2076-3417</issn><issn>2076-3417</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpNUU1LAzEQDaJgqT35BwIepTaTZD9yLMV-QEWheg5pdtamrJs12UX77922Is5lZt68efNgCLkF9iCEYhPTNABMQsbFBRlwlqVj0XeX_-prMopxz_pQIHJgA-Kn8ye6abviQH1J2x3SVV1WHdYWj8CiOlgMvqLzyn9RX9OlDxGDKVzc0Zd-8u0KE5HWaMJp29UT37V07U7IBm3rfB2PUobOvKtuyFVpqoij3zwkb_PH19lyvH5erGbT9diKVLa9WQYoi1Qibm0OQmwtT7ZZaXOTF4XkkCjDsgSMUGnWM5NSJVwVTCqFXFgQQ7I66xbe7HUT3IcJB-2N0yfAh3dtQutshRqVQZlLwXNQ0tpM8STjYIwQAFKV2GvdnbWa4D87jK3e-y7UvX3NEyFTyPIk7Vn3Z5YNPsaA5d9VYPr4IP3vQeIHIJ2Aiw</recordid><startdate>20210201</startdate><enddate>20210201</enddate><creator>Ivanov, Yuri D.</creator><creator>Pleshakova, Tatyana O.</creator><creator>Shumov, Ivan D.</creator><creator>Kozlov, Andrey F.</creator><creator>Ivanova, Irina A.</creator><creator>Ershova, Maria O.</creator><creator>Tatur, Vadim Yu</creator><creator>Ziborov, Vadim S.</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope></search><sort><creationdate>20210201</creationdate><title>AFM Study of the Influence of Glycerol Flow on Horseradish Peroxidase near the in/out Linear Sections of a Coil</title><author>Ivanov, Yuri D. ; Pleshakova, Tatyana O. ; Shumov, Ivan D. ; Kozlov, Andrey F. ; Ivanova, Irina A. ; Ershova, Maria O. ; Tatur, Vadim Yu ; Ziborov, Vadim S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c364t-3401e4d64eebc8133bc25b7fc8a8dd42159a0751a39671e45f9529d0499e23c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adsorption</topic><topic>Atomic force microscopy</topic><topic>Bioreactors</topic><topic>Biosensors</topic><topic>Electromagnetic fields</topic><topic>Electromagnetism</topic><topic>Enzymatic activity</topic><topic>Enzymes</topic><topic>Experiments</topic><topic>Flow</topic><topic>Glycerol</topic><topic>Heat transfer</topic><topic>Hemodynamics</topic><topic>Horseradish peroxidase</topic><topic>Hrp protein</topic><topic>liquid flow</topic><topic>Macromolecules</topic><topic>Outflow</topic><topic>Peroxidase</topic><topic>Pipes</topic><topic>Protein adsorption</topic><topic>protein aggregation</topic><topic>Proteins</topic><topic>Spectrophotometry</topic><topic>Structure-function relationships</topic><topic>triboelectric effect</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ivanov, Yuri D.</creatorcontrib><creatorcontrib>Pleshakova, Tatyana O.</creatorcontrib><creatorcontrib>Shumov, Ivan D.</creatorcontrib><creatorcontrib>Kozlov, Andrey F.</creatorcontrib><creatorcontrib>Ivanova, Irina A.</creatorcontrib><creatorcontrib>Ershova, Maria O.</creatorcontrib><creatorcontrib>Tatur, Vadim Yu</creatorcontrib><creatorcontrib>Ziborov, Vadim S.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Applied sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ivanov, Yuri D.</au><au>Pleshakova, Tatyana O.</au><au>Shumov, Ivan D.</au><au>Kozlov, Andrey F.</au><au>Ivanova, Irina A.</au><au>Ershova, Maria O.</au><au>Tatur, Vadim Yu</au><au>Ziborov, Vadim S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>AFM Study of the Influence of Glycerol Flow on Horseradish Peroxidase near the in/out Linear Sections of a Coil</atitle><jtitle>Applied sciences</jtitle><date>2021-02-01</date><risdate>2021</risdate><volume>11</volume><issue>4</issue><spage>1723</spage><pages>1723-</pages><issn>2076-3417</issn><eissn>2076-3417</eissn><abstract>Flow-based coiled systems, through which a heat transfer fluid (such as glycerol) is pumped, are widely used for thermal stabilization of bioreactors and biosensor cuvettes and cells. Previously, using horseradish peroxidase (HRP) as a model protein, we have demonstrated that the incubation of a protein solution in a flow-based system over coiled pipe with flowing glycerol leads to a change in the adsorption properties of the protein macromolecules. Herein, we have studied the effect of the glycerol flow on the properties of HRP, the solution of which was placed differently: i.e., near either the inflow or the outflow linear sections of the pipe, while the coiled section of the pipe was shielded with a grounded metallic cover. Atomic force microscopy (AFM) has been employed in order to visualize the HRP protein macromolecules adsorbed from its solution onto the mica substrate surface. The quantity of adsorbed protein was estimated based on the AFM data. The enzymatic activity of HRP was estimated by spectrophotometry. We demonstrate that a change in the properties of HRP enzyme was observed after the incubation of its solution near the inflow/outflow linear sections of the pipe with flowing glycerol. Namely, after the incubation of HRP solution near the inflow section, a decrease in the protein adsorption onto mica was observed, but its enzymatic activity remained unchanged in comparison to the control sample. In another case, when the HRP solution was incubated near the outflow section, an increased protein adsorption was observed, while the enzyme exhibited considerably lower activity.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/app11041723</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adsorption Atomic force microscopy Bioreactors Biosensors Electromagnetic fields Electromagnetism Enzymatic activity Enzymes Experiments Flow Glycerol Heat transfer Hemodynamics Horseradish peroxidase Hrp protein liquid flow Macromolecules Outflow Peroxidase Pipes Protein adsorption protein aggregation Proteins Spectrophotometry Structure-function relationships triboelectric effect |
title | AFM Study of the Influence of Glycerol Flow on Horseradish Peroxidase near the in/out Linear Sections of a Coil |
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