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Quinaldine Red as a fluorescent probe for determining the melting temperature () of proteins: a simple, rapid and high-throughput assay
Proteins play an important role in biological systems and several proteins are used in diagnosis, therapy, food industry etc. Thus, knowledge about the physical properties of the proteins is of utmost importance, which will aid in understanding their function and subsequent applications. The melting...
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Published in: | Analytical methods 2024-02, Vol.16 (6), p.95-956 |
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container_title | Analytical methods |
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creator | Das, Dhruv Sen, Vikram Chakraborty, Goutam Pillai, Vinayaki Tambade, Rahul Jonnalagadda, Padma Nilaya Rao, A. V. S. S. Narayana Chittela, Rajani Kant |
description | Proteins play an important role in biological systems and several proteins are used in diagnosis, therapy, food industry
etc.
Thus, knowledge about the physical properties of the proteins is of utmost importance, which will aid in understanding their function and subsequent applications. The melting temperature (
T
m
) of a protein is one of the essential parameters which gives information about the stability of a protein under different conditions. In the present study, we have demonstrated a method for determining the
T
m
of proteins using the supramolecular interaction between Quinaldine Red (QR) and proteins. Using this method, we have determined the
T
m
of 5 proteins and compared our results with established protocols. Our results showed good agreement with the other methods and published values. The method developed in this study is inexpensive, quick, and devoid of complex instruments and pre/post-treatment of the samples. In addition, this method can be adopted for high throughput in multi-plate mode. Thus, this study projects a new methodology for
T
m
determination of various proteins with user friendly operation.
A Quinaldine Red (QR) based method for measuring the
T
m
of proteins: differential binding of Quinaldine Red (QR) dye to native, partially unfolded and completely unfolded proteins allowed to measure the melting temperature (
T
m
) of the protein. |
doi_str_mv | 10.1039/d3ay01941a |
format | article |
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etc.
Thus, knowledge about the physical properties of the proteins is of utmost importance, which will aid in understanding their function and subsequent applications. The melting temperature (
T
m
) of a protein is one of the essential parameters which gives information about the stability of a protein under different conditions. In the present study, we have demonstrated a method for determining the
T
m
of proteins using the supramolecular interaction between Quinaldine Red (QR) and proteins. Using this method, we have determined the
T
m
of 5 proteins and compared our results with established protocols. Our results showed good agreement with the other methods and published values. The method developed in this study is inexpensive, quick, and devoid of complex instruments and pre/post-treatment of the samples. In addition, this method can be adopted for high throughput in multi-plate mode. Thus, this study projects a new methodology for
T
m
determination of various proteins with user friendly operation.
A Quinaldine Red (QR) based method for measuring the
T
m
of proteins: differential binding of Quinaldine Red (QR) dye to native, partially unfolded and completely unfolded proteins allowed to measure the melting temperature (
T
m
) of the protein.</description><identifier>ISSN: 1759-9660</identifier><identifier>EISSN: 1759-9679</identifier><identifier>DOI: 10.1039/d3ay01941a</identifier><identifier>PMID: 38291911</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Fluorescent indicators ; Food industry ; Melt temperature ; Melting ; Physical properties ; Proteins</subject><ispartof>Analytical methods, 2024-02, Vol.16 (6), p.95-956</ispartof><rights>Copyright Royal Society of Chemistry 2024</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c296t-59f51aa517e6858b3f9ab98682d04ab5418d8d048115b5d93d44d50afcd443ae3</cites><orcidid>0000-0002-5512-9632 ; 0009-0002-3254-8612 ; 0000-0003-1449-8244 ; 0000-0002-3439-8614</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38291911$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Das, Dhruv</creatorcontrib><creatorcontrib>Sen, Vikram</creatorcontrib><creatorcontrib>Chakraborty, Goutam</creatorcontrib><creatorcontrib>Pillai, Vinayaki</creatorcontrib><creatorcontrib>Tambade, Rahul</creatorcontrib><creatorcontrib>Jonnalagadda, Padma Nilaya</creatorcontrib><creatorcontrib>Rao, A. V. S. S. Narayana</creatorcontrib><creatorcontrib>Chittela, Rajani Kant</creatorcontrib><title>Quinaldine Red as a fluorescent probe for determining the melting temperature () of proteins: a simple, rapid and high-throughput assay</title><title>Analytical methods</title><addtitle>Anal Methods</addtitle><description>Proteins play an important role in biological systems and several proteins are used in diagnosis, therapy, food industry
etc.
Thus, knowledge about the physical properties of the proteins is of utmost importance, which will aid in understanding their function and subsequent applications. The melting temperature (
T
m
) of a protein is one of the essential parameters which gives information about the stability of a protein under different conditions. In the present study, we have demonstrated a method for determining the
T
m
of proteins using the supramolecular interaction between Quinaldine Red (QR) and proteins. Using this method, we have determined the
T
m
of 5 proteins and compared our results with established protocols. Our results showed good agreement with the other methods and published values. The method developed in this study is inexpensive, quick, and devoid of complex instruments and pre/post-treatment of the samples. In addition, this method can be adopted for high throughput in multi-plate mode. Thus, this study projects a new methodology for
T
m
determination of various proteins with user friendly operation.
A Quinaldine Red (QR) based method for measuring the
T
m
of proteins: differential binding of Quinaldine Red (QR) dye to native, partially unfolded and completely unfolded proteins allowed to measure the melting temperature (
T
m
) of the protein.</description><subject>Fluorescent indicators</subject><subject>Food industry</subject><subject>Melt temperature</subject><subject>Melting</subject><subject>Physical properties</subject><subject>Proteins</subject><issn>1759-9660</issn><issn>1759-9679</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpdkUtr3TAQhUVpadK0m-5bBN0kpU4ly7Kl7i5J-oBASUgWWZmxNb5W8Ct6LO4v6N-ucm9yCwXBHNCnM6M5hLzn7JQzob8aARvGdcHhBTnkldSZLiv9cq9LdkDeeH_PWKlFyV-TA6FyzTXnh-TPVbQTDMZOSK_RUPAUaDfE2aFvcQp0cXODtJsdNRjQjXay05qGHumIQ9hqHBd0EKJDenxC5-7xTUA7-W_Jy9txGfALdbDYZD8Z2tt1n4XezXHdLzGklh42b8mrDgaP757qEbn9fnFz9jO7_P3j19nqMmtzXYZM6k5yAMkrLJVUjeg0NFqVKjesgEYWXBmVpOJcNtJoYYrCSAZdm4QAFEfkeOebZnyI6EM92vTRYYAJ5-jrXOdMVnmlqoR--g-9n6NLy9pSIlfpqER93lGtm7132NWLsyO4Tc1Z_RhPfS5Wd9t4Vgn--GQZmxHNHn3OIwEfdoDz7f72X77iL_LqlQY</recordid><startdate>20240208</startdate><enddate>20240208</enddate><creator>Das, Dhruv</creator><creator>Sen, Vikram</creator><creator>Chakraborty, Goutam</creator><creator>Pillai, Vinayaki</creator><creator>Tambade, Rahul</creator><creator>Jonnalagadda, Padma Nilaya</creator><creator>Rao, A. V. S. S. Narayana</creator><creator>Chittela, Rajani Kant</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SE</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>FR3</scope><scope>H8G</scope><scope>JG9</scope><scope>L7M</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5512-9632</orcidid><orcidid>https://orcid.org/0009-0002-3254-8612</orcidid><orcidid>https://orcid.org/0000-0003-1449-8244</orcidid><orcidid>https://orcid.org/0000-0002-3439-8614</orcidid></search><sort><creationdate>20240208</creationdate><title>Quinaldine Red as a fluorescent probe for determining the melting temperature () of proteins: a simple, rapid and high-throughput assay</title><author>Das, Dhruv ; Sen, Vikram ; Chakraborty, Goutam ; Pillai, Vinayaki ; Tambade, Rahul ; Jonnalagadda, Padma Nilaya ; Rao, A. V. S. S. Narayana ; Chittela, Rajani Kant</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c296t-59f51aa517e6858b3f9ab98682d04ab5418d8d048115b5d93d44d50afcd443ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Fluorescent indicators</topic><topic>Food industry</topic><topic>Melt temperature</topic><topic>Melting</topic><topic>Physical properties</topic><topic>Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Das, Dhruv</creatorcontrib><creatorcontrib>Sen, Vikram</creatorcontrib><creatorcontrib>Chakraborty, Goutam</creatorcontrib><creatorcontrib>Pillai, Vinayaki</creatorcontrib><creatorcontrib>Tambade, Rahul</creatorcontrib><creatorcontrib>Jonnalagadda, Padma Nilaya</creatorcontrib><creatorcontrib>Rao, A. V. S. S. Narayana</creatorcontrib><creatorcontrib>Chittela, Rajani Kant</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Das, Dhruv</au><au>Sen, Vikram</au><au>Chakraborty, Goutam</au><au>Pillai, Vinayaki</au><au>Tambade, Rahul</au><au>Jonnalagadda, Padma Nilaya</au><au>Rao, A. V. S. S. Narayana</au><au>Chittela, Rajani Kant</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quinaldine Red as a fluorescent probe for determining the melting temperature () of proteins: a simple, rapid and high-throughput assay</atitle><jtitle>Analytical methods</jtitle><addtitle>Anal Methods</addtitle><date>2024-02-08</date><risdate>2024</risdate><volume>16</volume><issue>6</issue><spage>95</spage><epage>956</epage><pages>95-956</pages><issn>1759-9660</issn><eissn>1759-9679</eissn><abstract>Proteins play an important role in biological systems and several proteins are used in diagnosis, therapy, food industry
etc.
Thus, knowledge about the physical properties of the proteins is of utmost importance, which will aid in understanding their function and subsequent applications. The melting temperature (
T
m
) of a protein is one of the essential parameters which gives information about the stability of a protein under different conditions. In the present study, we have demonstrated a method for determining the
T
m
of proteins using the supramolecular interaction between Quinaldine Red (QR) and proteins. Using this method, we have determined the
T
m
of 5 proteins and compared our results with established protocols. Our results showed good agreement with the other methods and published values. The method developed in this study is inexpensive, quick, and devoid of complex instruments and pre/post-treatment of the samples. In addition, this method can be adopted for high throughput in multi-plate mode. Thus, this study projects a new methodology for
T
m
determination of various proteins with user friendly operation.
A Quinaldine Red (QR) based method for measuring the
T
m
of proteins: differential binding of Quinaldine Red (QR) dye to native, partially unfolded and completely unfolded proteins allowed to measure the melting temperature (
T
m
) of the protein.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>38291911</pmid><doi>10.1039/d3ay01941a</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-5512-9632</orcidid><orcidid>https://orcid.org/0009-0002-3254-8612</orcidid><orcidid>https://orcid.org/0000-0003-1449-8244</orcidid><orcidid>https://orcid.org/0000-0002-3439-8614</orcidid></addata></record> |
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source | Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list) |
subjects | Fluorescent indicators Food industry Melt temperature Melting Physical properties Proteins |
title | Quinaldine Red as a fluorescent probe for determining the melting temperature () of proteins: a simple, rapid and high-throughput assay |
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