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Chemically labeled ThUBD permits rapid and super-sensitive imaging of polyubiquitination signals
Polyubiquitination signal deliver diverse cellular signal, which have been recognized as a sophisticated ubiquitin code. The perception and transduction of ubiquitination signal depend on the specificity and sensitivity of the ubiquitin-binding domain. Accurate and sensitive detection of polyubiquit...
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Published in: | Analyst (London) 2022-07, Vol.147 (15), p.3434-3443 |
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container_title | Analyst (London) |
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creator | Xiao, Weidi Huang, Shuai Gao, Yuan Liu, Tong Li, Naikang Sui, Xinying Wang, Yonghong Yang, Guan Chang, Lei Kang, Xianjiang Duan, Changzhu Qin, Weijie Xu, Ping Li, Yanchang |
description | Polyubiquitination signal deliver diverse cellular signal, which have been recognized as a sophisticated ubiquitin code. The perception and transduction of ubiquitination signal depend on the specificity and sensitivity of the ubiquitin-binding domain. Accurate and sensitive detection of polyubiquitination signal is crucial for revealing the dynamic cellular ubiquitin-regulated events. Western blotting (WB) and immunohistochemistry (IHC) are the most widely used biochemical strategies to detect ubiquitination signal on substrates under diverse physiological and pathological conditions. However, anti-ubiquitin antibodies fail to reflect polyubiquitination signal unbiasedly because of their strong preference for K63-linked ubiquitin chains. Herein, we demonstrated that our previously developed tandem hybrid ubiquitin-binding domain (ThUBD) chemically labeled with a reporter group such as horseradish peroxidase (ThUBD-HRP) could significantly improve the robustness and sensitivity of polyubiquitination signal detection. This advanced method was named TUF-WB Plus (TUF-WB
+
). The TUF-WB
+
method significantly increases the sensitivity and accuracy of ubiquitin detection and requires a shorter experimental operation time. Furthermore, it enables the ThUBD-HRP probe to function as a powerful tool for spatial
in situ
polyubiquitination detection in cells by immunohistochemistry. Our newly developed ThUBD-HRP probe and TUF-WB
+
method provide a robust and powerful tool for ubiquitination signal detection with hypersensitivity in an unbiased manner.
The ThUBD-HRP probe and the consequential developed TUF-WB
+
method can detect polyubiquitination signal through one-step incubation with hypersensitivity, unbiased detection and a shorter operation time compared with the antibody method. |
doi_str_mv | 10.1039/d2an00577h |
format | article |
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+
). The TUF-WB
+
method significantly increases the sensitivity and accuracy of ubiquitin detection and requires a shorter experimental operation time. Furthermore, it enables the ThUBD-HRP probe to function as a powerful tool for spatial
in situ
polyubiquitination detection in cells by immunohistochemistry. Our newly developed ThUBD-HRP probe and TUF-WB
+
method provide a robust and powerful tool for ubiquitination signal detection with hypersensitivity in an unbiased manner.
The ThUBD-HRP probe and the consequential developed TUF-WB
+
method can detect polyubiquitination signal through one-step incubation with hypersensitivity, unbiased detection and a shorter operation time compared with the antibody method.</description><identifier>ISSN: 0003-2654</identifier><identifier>EISSN: 1364-5528</identifier><identifier>DOI: 10.1039/d2an00577h</identifier><language>eng</language><publisher>London: Royal Society of Chemistry</publisher><subject>Antibodies ; Binding ; Domains ; Peroxidase ; Sensitivity ; Signal detection ; Substrates</subject><ispartof>Analyst (London), 2022-07, Vol.147 (15), p.3434-3443</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c314t-f154aa8da75f3f0a1a53cdb837d0ca652fbdb0602bc79c8d38b575d40db5bf123</citedby><cites>FETCH-LOGICAL-c314t-f154aa8da75f3f0a1a53cdb837d0ca652fbdb0602bc79c8d38b575d40db5bf123</cites><orcidid>0000-0002-4177-3726 ; 0000-0002-7633-9786</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></links><search><creatorcontrib>Xiao, Weidi</creatorcontrib><creatorcontrib>Huang, Shuai</creatorcontrib><creatorcontrib>Gao, Yuan</creatorcontrib><creatorcontrib>Liu, Tong</creatorcontrib><creatorcontrib>Li, Naikang</creatorcontrib><creatorcontrib>Sui, Xinying</creatorcontrib><creatorcontrib>Wang, Yonghong</creatorcontrib><creatorcontrib>Yang, Guan</creatorcontrib><creatorcontrib>Chang, Lei</creatorcontrib><creatorcontrib>Kang, Xianjiang</creatorcontrib><creatorcontrib>Duan, Changzhu</creatorcontrib><creatorcontrib>Qin, Weijie</creatorcontrib><creatorcontrib>Xu, Ping</creatorcontrib><creatorcontrib>Li, Yanchang</creatorcontrib><title>Chemically labeled ThUBD permits rapid and super-sensitive imaging of polyubiquitination signals</title><title>Analyst (London)</title><description>Polyubiquitination signal deliver diverse cellular signal, which have been recognized as a sophisticated ubiquitin code. The perception and transduction of ubiquitination signal depend on the specificity and sensitivity of the ubiquitin-binding domain. Accurate and sensitive detection of polyubiquitination signal is crucial for revealing the dynamic cellular ubiquitin-regulated events. Western blotting (WB) and immunohistochemistry (IHC) are the most widely used biochemical strategies to detect ubiquitination signal on substrates under diverse physiological and pathological conditions. However, anti-ubiquitin antibodies fail to reflect polyubiquitination signal unbiasedly because of their strong preference for K63-linked ubiquitin chains. Herein, we demonstrated that our previously developed tandem hybrid ubiquitin-binding domain (ThUBD) chemically labeled with a reporter group such as horseradish peroxidase (ThUBD-HRP) could significantly improve the robustness and sensitivity of polyubiquitination signal detection. This advanced method was named TUF-WB Plus (TUF-WB
+
). The TUF-WB
+
method significantly increases the sensitivity and accuracy of ubiquitin detection and requires a shorter experimental operation time. Furthermore, it enables the ThUBD-HRP probe to function as a powerful tool for spatial
in situ
polyubiquitination detection in cells by immunohistochemistry. Our newly developed ThUBD-HRP probe and TUF-WB
+
method provide a robust and powerful tool for ubiquitination signal detection with hypersensitivity in an unbiased manner.
The ThUBD-HRP probe and the consequential developed TUF-WB
+
method can detect polyubiquitination signal through one-step incubation with hypersensitivity, unbiased detection and a shorter operation time compared with the antibody method.</description><subject>Antibodies</subject><subject>Binding</subject><subject>Domains</subject><subject>Peroxidase</subject><subject>Sensitivity</subject><subject>Signal detection</subject><subject>Substrates</subject><issn>0003-2654</issn><issn>1364-5528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpdkctLAzEQxoMoWKsX70LAiwireWw2u0dt1QpFL-15zWvblOyjya7Q_97UioIw8DEzP4aZbwC4xOgOI1rcayIahBjn6yMwwjRLE8ZIfgxGCCGakIylp-AshE1MMWJoBD4ma1NbJZzbQSekcUbDxXr5OIWd8bXtA_SisxqKRsMwxFoSTBNsbz8NtLVY2WYF2wp2rdsN0m6H2GlEb9sGBrtqhAvn4KSKYi5-dAyWz0-LySyZv7-8Th7miaI47ZMKs1SIXAvOKlohgQWjSsucco2UyBippJYoQ0QqXqhc01wyznSKtGSywoSOwc1hbufb7WBCX9Y2KOOcaEw7hJJkOeeEUlRE9PofumkHv182UsU-csYjdXuglG9D8KYqOx8v9rsSo3JvdjklD2_fZs8ifHWAfVC_3N8z6Be4mXzc</recordid><startdate>20220722</startdate><enddate>20220722</enddate><creator>Xiao, Weidi</creator><creator>Huang, Shuai</creator><creator>Gao, Yuan</creator><creator>Liu, Tong</creator><creator>Li, Naikang</creator><creator>Sui, Xinying</creator><creator>Wang, Yonghong</creator><creator>Yang, Guan</creator><creator>Chang, Lei</creator><creator>Kang, Xianjiang</creator><creator>Duan, Changzhu</creator><creator>Qin, Weijie</creator><creator>Xu, Ping</creator><creator>Li, Yanchang</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4177-3726</orcidid><orcidid>https://orcid.org/0000-0002-7633-9786</orcidid></search><sort><creationdate>20220722</creationdate><title>Chemically labeled ThUBD permits rapid and super-sensitive imaging of polyubiquitination signals</title><author>Xiao, Weidi ; Huang, Shuai ; Gao, Yuan ; Liu, Tong ; Li, Naikang ; Sui, Xinying ; Wang, Yonghong ; Yang, Guan ; Chang, Lei ; Kang, Xianjiang ; Duan, Changzhu ; Qin, Weijie ; Xu, Ping ; Li, Yanchang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c314t-f154aa8da75f3f0a1a53cdb837d0ca652fbdb0602bc79c8d38b575d40db5bf123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antibodies</topic><topic>Binding</topic><topic>Domains</topic><topic>Peroxidase</topic><topic>Sensitivity</topic><topic>Signal detection</topic><topic>Substrates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xiao, Weidi</creatorcontrib><creatorcontrib>Huang, Shuai</creatorcontrib><creatorcontrib>Gao, Yuan</creatorcontrib><creatorcontrib>Liu, Tong</creatorcontrib><creatorcontrib>Li, Naikang</creatorcontrib><creatorcontrib>Sui, Xinying</creatorcontrib><creatorcontrib>Wang, Yonghong</creatorcontrib><creatorcontrib>Yang, Guan</creatorcontrib><creatorcontrib>Chang, Lei</creatorcontrib><creatorcontrib>Kang, Xianjiang</creatorcontrib><creatorcontrib>Duan, Changzhu</creatorcontrib><creatorcontrib>Qin, Weijie</creatorcontrib><creatorcontrib>Xu, Ping</creatorcontrib><creatorcontrib>Li, Yanchang</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Analyst (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xiao, Weidi</au><au>Huang, Shuai</au><au>Gao, Yuan</au><au>Liu, Tong</au><au>Li, Naikang</au><au>Sui, Xinying</au><au>Wang, Yonghong</au><au>Yang, Guan</au><au>Chang, Lei</au><au>Kang, Xianjiang</au><au>Duan, Changzhu</au><au>Qin, Weijie</au><au>Xu, Ping</au><au>Li, Yanchang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chemically labeled ThUBD permits rapid and super-sensitive imaging of polyubiquitination signals</atitle><jtitle>Analyst (London)</jtitle><date>2022-07-22</date><risdate>2022</risdate><volume>147</volume><issue>15</issue><spage>3434</spage><epage>3443</epage><pages>3434-3443</pages><issn>0003-2654</issn><eissn>1364-5528</eissn><abstract>Polyubiquitination signal deliver diverse cellular signal, which have been recognized as a sophisticated ubiquitin code. The perception and transduction of ubiquitination signal depend on the specificity and sensitivity of the ubiquitin-binding domain. Accurate and sensitive detection of polyubiquitination signal is crucial for revealing the dynamic cellular ubiquitin-regulated events. Western blotting (WB) and immunohistochemistry (IHC) are the most widely used biochemical strategies to detect ubiquitination signal on substrates under diverse physiological and pathological conditions. However, anti-ubiquitin antibodies fail to reflect polyubiquitination signal unbiasedly because of their strong preference for K63-linked ubiquitin chains. Herein, we demonstrated that our previously developed tandem hybrid ubiquitin-binding domain (ThUBD) chemically labeled with a reporter group such as horseradish peroxidase (ThUBD-HRP) could significantly improve the robustness and sensitivity of polyubiquitination signal detection. This advanced method was named TUF-WB Plus (TUF-WB
+
). The TUF-WB
+
method significantly increases the sensitivity and accuracy of ubiquitin detection and requires a shorter experimental operation time. Furthermore, it enables the ThUBD-HRP probe to function as a powerful tool for spatial
in situ
polyubiquitination detection in cells by immunohistochemistry. Our newly developed ThUBD-HRP probe and TUF-WB
+
method provide a robust and powerful tool for ubiquitination signal detection with hypersensitivity in an unbiased manner.
The ThUBD-HRP probe and the consequential developed TUF-WB
+
method can detect polyubiquitination signal through one-step incubation with hypersensitivity, unbiased detection and a shorter operation time compared with the antibody method.</abstract><cop>London</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2an00577h</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-4177-3726</orcidid><orcidid>https://orcid.org/0000-0002-7633-9786</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 | Antibodies Binding Domains Peroxidase Sensitivity Signal detection Substrates |
title | Chemically labeled ThUBD permits rapid and super-sensitive imaging of polyubiquitination signals |
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