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Artificial metalloenzymes based on protein assembly
[Display omitted] •Protein self-assembly and their importance in developing artificial metalloenzyme compared to monomeric counterpart.•Catalytic activities by various artificial metalloenzymes based on protein assembly.•Recent development of metalloprotein assembly design and construction. Metalloe...
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Published in: | Coordination chemistry reviews 2022-10, Vol.469, p.214593, Article 214593 |
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creator | Maity, Basudev Taher, Mohd Mazumdar, Shyamalava Ueno, Takafumi |
description | [Display omitted]
•Protein self-assembly and their importance in developing artificial metalloenzyme compared to monomeric counterpart.•Catalytic activities by various artificial metalloenzymes based on protein assembly.•Recent development of metalloprotein assembly design and construction.
Metalloenzymes play essential roles in biology, whereas artificial metalloenzymes use synthetic metal cofactors for promoting non-natural reactions. In the past decades, tremendous advances have been made in manipulating artificial metalloenzymes for various organic transformation reactions, including C–H activation, C–C coupling, transfer hydrogenation, etc. Advanced methods like “Directed evolution,” “high throughput screening,” and “rational design” have stimulated the artificial metalloenzyme research. Applications of artificial metalloenzymes have been extended to cells for controlling functions like prodrug activation. Usually, for more complicated processes like multistep reactions or isolation of reaction environments, nature uses sophisticated strategies, such as positional assembly and compartmentalization of catalysts. However, artificial metalloenzyme research in this direction is relatively less. Several researchers have designed and constructed various protein assembly structures through metal coordination. However, only a few of them have been tested for catalytic activities. Assembled metalloenzymes have multiple advantages like promoting multistep reactions, stabilizing the catalyst, cooperativity in the reaction, higher-order complexity, sophisticated structures, confinement of reaction, etc. Therefore, systematic investigations on their design, structure, and activity are necessary to represent them as next-generation biocatalysts. In this context, the current review highlights the importance of self-assembled metalloenzymes, available design strategies, current developments, catalytic activities, and the future direction of the research. |
doi_str_mv | 10.1016/j.ccr.2022.214593 |
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•Protein self-assembly and their importance in developing artificial metalloenzyme compared to monomeric counterpart.•Catalytic activities by various artificial metalloenzymes based on protein assembly.•Recent development of metalloprotein assembly design and construction.
Metalloenzymes play essential roles in biology, whereas artificial metalloenzymes use synthetic metal cofactors for promoting non-natural reactions. In the past decades, tremendous advances have been made in manipulating artificial metalloenzymes for various organic transformation reactions, including C–H activation, C–C coupling, transfer hydrogenation, etc. Advanced methods like “Directed evolution,” “high throughput screening,” and “rational design” have stimulated the artificial metalloenzyme research. Applications of artificial metalloenzymes have been extended to cells for controlling functions like prodrug activation. Usually, for more complicated processes like multistep reactions or isolation of reaction environments, nature uses sophisticated strategies, such as positional assembly and compartmentalization of catalysts. However, artificial metalloenzyme research in this direction is relatively less. Several researchers have designed and constructed various protein assembly structures through metal coordination. However, only a few of them have been tested for catalytic activities. Assembled metalloenzymes have multiple advantages like promoting multistep reactions, stabilizing the catalyst, cooperativity in the reaction, higher-order complexity, sophisticated structures, confinement of reaction, etc. Therefore, systematic investigations on their design, structure, and activity are necessary to represent them as next-generation biocatalysts. In this context, the current review highlights the importance of self-assembled metalloenzymes, available design strategies, current developments, catalytic activities, and the future direction of the research.</description><identifier>ISSN: 0010-8545</identifier><identifier>EISSN: 1873-3840</identifier><identifier>DOI: 10.1016/j.ccr.2022.214593</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Artificial metalloenzyme ; Catalysis ; Metalloprotein assembly design ; Protein self-assembly</subject><ispartof>Coordination chemistry reviews, 2022-10, Vol.469, p.214593, Article 214593</ispartof><rights>2022 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c380t-6b27dd96637d54a9d1b075cb36bd4b440958a2089e56b81a401e6dc1659d6db23</citedby><cites>FETCH-LOGICAL-c380t-6b27dd96637d54a9d1b075cb36bd4b440958a2089e56b81a401e6dc1659d6db23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Maity, Basudev</creatorcontrib><creatorcontrib>Taher, Mohd</creatorcontrib><creatorcontrib>Mazumdar, Shyamalava</creatorcontrib><creatorcontrib>Ueno, Takafumi</creatorcontrib><title>Artificial metalloenzymes based on protein assembly</title><title>Coordination chemistry reviews</title><description>[Display omitted]
•Protein self-assembly and their importance in developing artificial metalloenzyme compared to monomeric counterpart.•Catalytic activities by various artificial metalloenzymes based on protein assembly.•Recent development of metalloprotein assembly design and construction.
Metalloenzymes play essential roles in biology, whereas artificial metalloenzymes use synthetic metal cofactors for promoting non-natural reactions. In the past decades, tremendous advances have been made in manipulating artificial metalloenzymes for various organic transformation reactions, including C–H activation, C–C coupling, transfer hydrogenation, etc. Advanced methods like “Directed evolution,” “high throughput screening,” and “rational design” have stimulated the artificial metalloenzyme research. Applications of artificial metalloenzymes have been extended to cells for controlling functions like prodrug activation. Usually, for more complicated processes like multistep reactions or isolation of reaction environments, nature uses sophisticated strategies, such as positional assembly and compartmentalization of catalysts. However, artificial metalloenzyme research in this direction is relatively less. Several researchers have designed and constructed various protein assembly structures through metal coordination. However, only a few of them have been tested for catalytic activities. Assembled metalloenzymes have multiple advantages like promoting multistep reactions, stabilizing the catalyst, cooperativity in the reaction, higher-order complexity, sophisticated structures, confinement of reaction, etc. Therefore, systematic investigations on their design, structure, and activity are necessary to represent them as next-generation biocatalysts. In this context, the current review highlights the importance of self-assembled metalloenzymes, available design strategies, current developments, catalytic activities, and the future direction of the research.</description><subject>Artificial metalloenzyme</subject><subject>Catalysis</subject><subject>Metalloprotein assembly design</subject><subject>Protein self-assembly</subject><issn>0010-8545</issn><issn>1873-3840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9j8tKAzEYhYMoWKsP4G5eYMY_10lwVYpaoeBG1yGXfyBlLiUZhPr0TqlrV4ez-A7nI-SRQkOBqqdDE0JuGDDWMCqk4VdkRXXLa64FXJMVAIVaSyFvyV0ph6UqY9iK8E2eU5dCcn014Oz6fsLx5zRgqbwrGKtprI55mjGNlSsFB9-f7slN5_qCD3-5Jl-vL5_bXb3_eHvfbvZ14BrmWnnWxmiU4m2UwplIPbQyeK58FF4IMFI7BtqgVF5TJ4CiioEqaaKKnvE1oZfdkKdSMnb2mNPg8slSsGdre7CLtT1b24v1wjxfGFyOfSfMtoSEY8CYMobZxin9Q_8CcmZfMg</recordid><startdate>202210</startdate><enddate>202210</enddate><creator>Maity, Basudev</creator><creator>Taher, Mohd</creator><creator>Mazumdar, Shyamalava</creator><creator>Ueno, Takafumi</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>202210</creationdate><title>Artificial metalloenzymes based on protein assembly</title><author>Maity, Basudev ; Taher, Mohd ; Mazumdar, Shyamalava ; Ueno, Takafumi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c380t-6b27dd96637d54a9d1b075cb36bd4b440958a2089e56b81a401e6dc1659d6db23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Artificial metalloenzyme</topic><topic>Catalysis</topic><topic>Metalloprotein assembly design</topic><topic>Protein self-assembly</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maity, Basudev</creatorcontrib><creatorcontrib>Taher, Mohd</creatorcontrib><creatorcontrib>Mazumdar, Shyamalava</creatorcontrib><creatorcontrib>Ueno, Takafumi</creatorcontrib><collection>CrossRef</collection><jtitle>Coordination chemistry reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maity, Basudev</au><au>Taher, Mohd</au><au>Mazumdar, Shyamalava</au><au>Ueno, Takafumi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Artificial metalloenzymes based on protein assembly</atitle><jtitle>Coordination chemistry reviews</jtitle><date>2022-10</date><risdate>2022</risdate><volume>469</volume><spage>214593</spage><pages>214593-</pages><artnum>214593</artnum><issn>0010-8545</issn><eissn>1873-3840</eissn><abstract>[Display omitted]
•Protein self-assembly and their importance in developing artificial metalloenzyme compared to monomeric counterpart.•Catalytic activities by various artificial metalloenzymes based on protein assembly.•Recent development of metalloprotein assembly design and construction.
Metalloenzymes play essential roles in biology, whereas artificial metalloenzymes use synthetic metal cofactors for promoting non-natural reactions. In the past decades, tremendous advances have been made in manipulating artificial metalloenzymes for various organic transformation reactions, including C–H activation, C–C coupling, transfer hydrogenation, etc. Advanced methods like “Directed evolution,” “high throughput screening,” and “rational design” have stimulated the artificial metalloenzyme research. Applications of artificial metalloenzymes have been extended to cells for controlling functions like prodrug activation. Usually, for more complicated processes like multistep reactions or isolation of reaction environments, nature uses sophisticated strategies, such as positional assembly and compartmentalization of catalysts. However, artificial metalloenzyme research in this direction is relatively less. Several researchers have designed and constructed various protein assembly structures through metal coordination. However, only a few of them have been tested for catalytic activities. Assembled metalloenzymes have multiple advantages like promoting multistep reactions, stabilizing the catalyst, cooperativity in the reaction, higher-order complexity, sophisticated structures, confinement of reaction, etc. Therefore, systematic investigations on their design, structure, and activity are necessary to represent them as next-generation biocatalysts. In this context, the current review highlights the importance of self-assembled metalloenzymes, available design strategies, current developments, catalytic activities, and the future direction of the research.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.ccr.2022.214593</doi><oa>free_for_read</oa></addata></record> |
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subjects | Artificial metalloenzyme Catalysis Metalloprotein assembly design Protein self-assembly |
title | Artificial metalloenzymes based on protein assembly |
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