Biological Nanopore Approach for Single‐Molecule Protein Sequencing
Proteins are responsible for the occurrence and treatment of many diseases, and therefore protein sequencing will revolutionize proteomics and clinical diagnostics. Biological nanopore approach has proved successful for single‐molecule DNA sequencing, which resolves the identities of 4 natural deoxy...
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Veröffentlicht in: | Angewandte Chemie 2021-06, Vol.133 (27), p.14862-14873 |
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description | Proteins are responsible for the occurrence and treatment of many diseases, and therefore protein sequencing will revolutionize proteomics and clinical diagnostics. Biological nanopore approach has proved successful for single‐molecule DNA sequencing, which resolves the identities of 4 natural deoxyribonucleotides based on the current blockages and duration times of their translocations across the nanopore confinement. However, open challenges still remain for biological nanopores to sequentially identify each amino acid (AA) of single proteins due to the inherent complexity of 20 proteinogenic AAs in charges, volumes, hydrophobicity and structures. Herein, we focus on recent exciting advances in biological nanopores for single‐molecule protein sequencing (SMPS) from native protein unfolding, control of peptide translocation, AA identification to applications in disease detection.
Nanopore electrochemistry offers a bright prospect for single‐molecule protein sequencing by measuring specific interactions between amino acids based on their natural structure and chemistry continuity and diversity. This Minireview focusses on recent advances in biological nanopores from protein unfolding, peptide translocation, amino acid identification to diagnostic application. |
doi_str_mv | 10.1002/ange.202013462 |
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Nanopore electrochemistry offers a bright prospect for single‐molecule protein sequencing by measuring specific interactions between amino acids based on their natural structure and chemistry continuity and diversity. This Minireview focusses on recent advances in biological nanopores from protein unfolding, peptide translocation, amino acid identification to diagnostic application.</description><identifier>ISSN: 0044-8249</identifier><identifier>EISSN: 1521-3757</identifier><identifier>DOI: 10.1002/ange.202013462</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Amino acids ; biological nanopore ; Chemistry ; Deoxyribonucleotides ; diagnostics ; Disease detection ; DNA sequencing ; Hydrophobicity ; nano-confinement ; Protein folding ; protein sequencing ; Proteins ; Proteomics ; single-molecule sensing ; Translocation</subject><ispartof>Angewandte Chemie, 2021-06, Vol.133 (27), p.14862-14873</ispartof><rights>2020 Wiley‐VCH GmbH</rights><rights>2021 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2282-d6816740d39c99ec52460be40cc616be77d7c430cd62206b150e815a6058041a3</citedby><cites>FETCH-LOGICAL-c2282-d6816740d39c99ec52460be40cc616be77d7c430cd62206b150e815a6058041a3</cites><orcidid>0000-0003-2571-7457 ; 0000-0001-6217-256X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fange.202013462$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fange.202013462$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids></links><search><creatorcontrib>Hu, Zheng‐Li</creatorcontrib><creatorcontrib>Huo, Ming‐Zhu</creatorcontrib><creatorcontrib>Ying, Yi‐Lun</creatorcontrib><creatorcontrib>Long, Yi‐Tao</creatorcontrib><title>Biological Nanopore Approach for Single‐Molecule Protein Sequencing</title><title>Angewandte Chemie</title><description>Proteins are responsible for the occurrence and treatment of many diseases, and therefore protein sequencing will revolutionize proteomics and clinical diagnostics. Biological nanopore approach has proved successful for single‐molecule DNA sequencing, which resolves the identities of 4 natural deoxyribonucleotides based on the current blockages and duration times of their translocations across the nanopore confinement. However, open challenges still remain for biological nanopores to sequentially identify each amino acid (AA) of single proteins due to the inherent complexity of 20 proteinogenic AAs in charges, volumes, hydrophobicity and structures. Herein, we focus on recent exciting advances in biological nanopores for single‐molecule protein sequencing (SMPS) from native protein unfolding, control of peptide translocation, AA identification to applications in disease detection.
Nanopore electrochemistry offers a bright prospect for single‐molecule protein sequencing by measuring specific interactions between amino acids based on their natural structure and chemistry continuity and diversity. This Minireview focusses on recent advances in biological nanopores from protein unfolding, peptide translocation, amino acid identification to diagnostic application.</description><subject>Amino acids</subject><subject>biological nanopore</subject><subject>Chemistry</subject><subject>Deoxyribonucleotides</subject><subject>diagnostics</subject><subject>Disease detection</subject><subject>DNA sequencing</subject><subject>Hydrophobicity</subject><subject>nano-confinement</subject><subject>Protein folding</subject><subject>protein sequencing</subject><subject>Proteins</subject><subject>Proteomics</subject><subject>single-molecule sensing</subject><subject>Translocation</subject><issn>0044-8249</issn><issn>1521-3757</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkE1Lw0AQhhdRsFavngOeU2dnv5JjLbUKtQrV87LdTGtKzMaNRXrzJ_gb_SWmVPToaQ7zPPMOL2PnHAYcAC9dvaIBAgIXUuMB63GFPBVGmUPWA5AyzVDmx-ykbdcAoNHkPTa-KkMVVqV3VTJzdWhCpGTYNDE4_5wsQ0zmZb2q6Ovj8y5U5DcVJQ8xvFFZJ3N63VDtu_0pO1q6qqWzn9lnT9fjx9FNOr2f3I6G09QjZpgWOuPaSChE7vOcvEKpYUESvNdcL8iYwngpwBcaEfSCK6CMK6dBZSC5E312sb_b_ddlt292HTax7iItKolKCy2yjhrsKR9D20Za2iaWLy5uLQe7q8ruqrK_VXVCvhfey4q2_9B2OJuM_9xvC3RsnA</recordid><startdate>20210625</startdate><enddate>20210625</enddate><creator>Hu, Zheng‐Li</creator><creator>Huo, Ming‐Zhu</creator><creator>Ying, Yi‐Lun</creator><creator>Long, Yi‐Tao</creator><general>Wiley Subscription Services, Inc</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><orcidid>https://orcid.org/0000-0003-2571-7457</orcidid><orcidid>https://orcid.org/0000-0001-6217-256X</orcidid></search><sort><creationdate>20210625</creationdate><title>Biological Nanopore Approach for Single‐Molecule Protein Sequencing</title><author>Hu, Zheng‐Li ; Huo, Ming‐Zhu ; Ying, Yi‐Lun ; Long, Yi‐Tao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2282-d6816740d39c99ec52460be40cc616be77d7c430cd62206b150e815a6058041a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Amino acids</topic><topic>biological nanopore</topic><topic>Chemistry</topic><topic>Deoxyribonucleotides</topic><topic>diagnostics</topic><topic>Disease detection</topic><topic>DNA sequencing</topic><topic>Hydrophobicity</topic><topic>nano-confinement</topic><topic>Protein folding</topic><topic>protein sequencing</topic><topic>Proteins</topic><topic>Proteomics</topic><topic>single-molecule sensing</topic><topic>Translocation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Zheng‐Li</creatorcontrib><creatorcontrib>Huo, Ming‐Zhu</creatorcontrib><creatorcontrib>Ying, Yi‐Lun</creatorcontrib><creatorcontrib>Long, Yi‐Tao</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><jtitle>Angewandte Chemie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Zheng‐Li</au><au>Huo, Ming‐Zhu</au><au>Ying, Yi‐Lun</au><au>Long, Yi‐Tao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biological Nanopore Approach for Single‐Molecule Protein Sequencing</atitle><jtitle>Angewandte Chemie</jtitle><date>2021-06-25</date><risdate>2021</risdate><volume>133</volume><issue>27</issue><spage>14862</spage><epage>14873</epage><pages>14862-14873</pages><issn>0044-8249</issn><eissn>1521-3757</eissn><abstract>Proteins are responsible for the occurrence and treatment of many diseases, and therefore protein sequencing will revolutionize proteomics and clinical diagnostics. Biological nanopore approach has proved successful for single‐molecule DNA sequencing, which resolves the identities of 4 natural deoxyribonucleotides based on the current blockages and duration times of their translocations across the nanopore confinement. However, open challenges still remain for biological nanopores to sequentially identify each amino acid (AA) of single proteins due to the inherent complexity of 20 proteinogenic AAs in charges, volumes, hydrophobicity and structures. Herein, we focus on recent exciting advances in biological nanopores for single‐molecule protein sequencing (SMPS) from native protein unfolding, control of peptide translocation, AA identification to applications in disease detection.
Nanopore electrochemistry offers a bright prospect for single‐molecule protein sequencing by measuring specific interactions between amino acids based on their natural structure and chemistry continuity and diversity. This Minireview focusses on recent advances in biological nanopores from protein unfolding, peptide translocation, amino acid identification to diagnostic application.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ange.202013462</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-2571-7457</orcidid><orcidid>https://orcid.org/0000-0001-6217-256X</orcidid></addata></record> |
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subjects | Amino acids biological nanopore Chemistry Deoxyribonucleotides diagnostics Disease detection DNA sequencing Hydrophobicity nano-confinement Protein folding protein sequencing Proteins Proteomics single-molecule sensing Translocation |
title | Biological Nanopore Approach for Single‐Molecule Protein Sequencing |
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