Deciphering the preference and predicting the viability of circular permutations in proteins
Circular permutation (CP) refers to situations in which the termini of a protein are relocated to other positions in the structure. CP occurs naturally and has been artificially created to study protein function, stability and folding. Recently CP is increasingly applied to engineer enzyme structure...
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description | Circular permutation (CP) refers to situations in which the termini of a protein are relocated to other positions in the structure. CP occurs naturally and has been artificially created to study protein function, stability and folding. Recently CP is increasingly applied to engineer enzyme structure and function, and to create bifunctional fusion proteins unachievable by tandem fusion. CP is a complicated and expensive technique. An intrinsic difficulty in its application lies in the fact that not every position in a protein is amenable for creating a viable permutant. To examine the preferences of CP and develop CP viability prediction methods, we carried out comprehensive analyses of the sequence, structural, and dynamical properties of known CP sites using a variety of statistics and simulation methods, such as the bootstrap aggregating, permutation test and molecular dynamics simulations. CP particularly favors Gly, Pro, Asp and Asn. Positions preferred by CP lie within coils, loops, turns, and at residues that are exposed to solvent, weakly hydrogen-bonded, environmentally unpacked, or flexible. Disfavored positions include Cys, bulky hydrophobic residues, and residues located within helices or near the protein's core. These results fostered the development of an effective viable CP site prediction system, which combined four machine learning methods, e.g., artificial neural networks, the support vector machine, a random forest, and a hierarchical feature integration procedure developed in this work. As assessed by using the hydrofolate reductase dataset as the independent evaluation dataset, this prediction system achieved an AUC of 0.9. Large-scale predictions have been performed for nine thousand representative protein structures; several new potential applications of CP were thus identified. Many unreported preferences of CP are revealed in this study. The developed system is the best CP viability prediction method currently available. This work will facilitate the application of CP in research and biotechnology. |
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CP occurs naturally and has been artificially created to study protein function, stability and folding. Recently CP is increasingly applied to engineer enzyme structure and function, and to create bifunctional fusion proteins unachievable by tandem fusion. CP is a complicated and expensive technique. An intrinsic difficulty in its application lies in the fact that not every position in a protein is amenable for creating a viable permutant. To examine the preferences of CP and develop CP viability prediction methods, we carried out comprehensive analyses of the sequence, structural, and dynamical properties of known CP sites using a variety of statistics and simulation methods, such as the bootstrap aggregating, permutation test and molecular dynamics simulations. CP particularly favors Gly, Pro, Asp and Asn. Positions preferred by CP lie within coils, loops, turns, and at residues that are exposed to solvent, weakly hydrogen-bonded, environmentally unpacked, or flexible. Disfavored positions include Cys, bulky hydrophobic residues, and residues located within helices or near the protein's core. These results fostered the development of an effective viable CP site prediction system, which combined four machine learning methods, e.g., artificial neural networks, the support vector machine, a random forest, and a hierarchical feature integration procedure developed in this work. As assessed by using the hydrofolate reductase dataset as the independent evaluation dataset, this prediction system achieved an AUC of 0.9. Large-scale predictions have been performed for nine thousand representative protein structures; several new potential applications of CP were thus identified. Many unreported preferences of CP are revealed in this study. The developed system is the best CP viability prediction method currently available. This work will facilitate the application of CP in research and biotechnology.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0031791</identifier><identifier>PMID: 22359629</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Algorithms ; Amino Acid Sequence ; Analysis ; Artificial intelligence ; Artificial neural networks ; Back propagation ; Biochemistry ; Bioinformatics ; Biology ; Biotechnology ; Bonding strength ; Chemical bonds ; Coiling ; Coils ; Computer Simulation ; Datasets ; Dihydrofolate reductase ; Enzymes ; Forest management ; Helices ; Hydrogen ; Hydrogen bonding ; Hydrogen bonds ; Hydrophobicity ; Learning algorithms ; Ligands ; Machine learning ; Models, Molecular ; Molecular biology ; Molecular dynamics ; Mutagenesis ; Neural networks ; Permutations ; Predictions ; Protein Engineering ; Protein folding ; Proteins ; Proteins - chemistry ; Reductase ; Researchers ; Residues ; Simulation ; Software packages ; Statistical methods ; Statistical tests ; Structural stability ; Structure-function relationships ; Support Vector Machine ; Viability</subject><ispartof>PloS one, 2012-02, Vol.7 (2), p.e31791-e31791</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Lo et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Lo et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c691t-3b0450424228e86eef9a820c6e9b26fb4f22a37cd0864dc580ff45194678b2563</citedby><cites>FETCH-LOGICAL-c691t-3b0450424228e86eef9a820c6e9b26fb4f22a37cd0864dc580ff45194678b2563</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281007/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281007/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,2096,2915,23847,27905,27906,53772,53774,79349,79350</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22359629$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Flower, Darren R.</contributor><creatorcontrib>Lo, Wei-Cheng</creatorcontrib><creatorcontrib>Dai, Tian</creatorcontrib><creatorcontrib>Liu, Yen-Yi</creatorcontrib><creatorcontrib>Wang, Li-Fen</creatorcontrib><creatorcontrib>Hwang, Jenn-Kang</creatorcontrib><creatorcontrib>Lyu, Ping-Chiang</creatorcontrib><title>Deciphering the preference and predicting the viability of circular permutations in proteins</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Circular permutation (CP) refers to situations in which the termini of a protein are relocated to other positions in the structure. CP occurs naturally and has been artificially created to study protein function, stability and folding. Recently CP is increasingly applied to engineer enzyme structure and function, and to create bifunctional fusion proteins unachievable by tandem fusion. CP is a complicated and expensive technique. An intrinsic difficulty in its application lies in the fact that not every position in a protein is amenable for creating a viable permutant. To examine the preferences of CP and develop CP viability prediction methods, we carried out comprehensive analyses of the sequence, structural, and dynamical properties of known CP sites using a variety of statistics and simulation methods, such as the bootstrap aggregating, permutation test and molecular dynamics simulations. CP particularly favors Gly, Pro, Asp and Asn. Positions preferred by CP lie within coils, loops, turns, and at residues that are exposed to solvent, weakly hydrogen-bonded, environmentally unpacked, or flexible. Disfavored positions include Cys, bulky hydrophobic residues, and residues located within helices or near the protein's core. These results fostered the development of an effective viable CP site prediction system, which combined four machine learning methods, e.g., artificial neural networks, the support vector machine, a random forest, and a hierarchical feature integration procedure developed in this work. As assessed by using the hydrofolate reductase dataset as the independent evaluation dataset, this prediction system achieved an AUC of 0.9. Large-scale predictions have been performed for nine thousand representative protein structures; several new potential applications of CP were thus identified. Many unreported preferences of CP are revealed in this study. The developed system is the best CP viability prediction method currently available. This work will facilitate the application of CP in research and biotechnology.</description><subject>Algorithms</subject><subject>Amino Acid Sequence</subject><subject>Analysis</subject><subject>Artificial intelligence</subject><subject>Artificial neural networks</subject><subject>Back propagation</subject><subject>Biochemistry</subject><subject>Bioinformatics</subject><subject>Biology</subject><subject>Biotechnology</subject><subject>Bonding strength</subject><subject>Chemical bonds</subject><subject>Coiling</subject><subject>Coils</subject><subject>Computer Simulation</subject><subject>Datasets</subject><subject>Dihydrofolate reductase</subject><subject>Enzymes</subject><subject>Forest management</subject><subject>Helices</subject><subject>Hydrogen</subject><subject>Hydrogen bonding</subject><subject>Hydrogen bonds</subject><subject>Hydrophobicity</subject><subject>Learning algorithms</subject><subject>Ligands</subject><subject>Machine learning</subject><subject>Models, Molecular</subject><subject>Molecular biology</subject><subject>Molecular dynamics</subject><subject>Mutagenesis</subject><subject>Neural networks</subject><subject>Permutations</subject><subject>Predictions</subject><subject>Protein Engineering</subject><subject>Protein folding</subject><subject>Proteins</subject><subject>Proteins - chemistry</subject><subject>Reductase</subject><subject>Researchers</subject><subject>Residues</subject><subject>Simulation</subject><subject>Software packages</subject><subject>Statistical methods</subject><subject>Statistical tests</subject><subject>Structural stability</subject><subject>Structure-function relationships</subject><subject>Support Vector Machine</subject><subject>Viability</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNk1uL1DAYhoso7jr6D0QLguLFjDk1TW6EZT0NLCx4uhJCmn6dydJpapIu7r833eksU9kL6UWb5HnfL_0OWfYcoxWmJX535Qbf6XbVuw5WCFFcSvwgO8WSkiUniD48-j7JnoRwhVBBBeePsxNCaCE5kafZrw9gbL8Fb7tNHreQ9x4a8NAZyHVXj8vamng4vba6sq2NN7lrcmO9GVrt8x78bog6WteF3HZJ5CLYLjzNHjW6DfBsei-yH58-fj__sry4_Lw-P7tYGi5xXNIKsQIxwggRIDhAI7UgyHCQFeFNxRpCNC1NjQRntSkEahpWYMl4KSpScLrIXu59-9YFNSUmKEwpJUxSNBLrPVE7faV6b3fa3yinrbrdcH6jtI_WtKAKEEZQXtaVoIxxIWhZE4MwAlHjQuvk9X6KNlQ7qA100et2Zjo_6exWbdy1okRghMpk8GYy8O73ACGqnQ0G2lZ34IagZKpOKWWq3iJ79Q95_89N1Ean-9uucSmsGT3VGStLJEa_RK3uodJTw86a1ESNTfszwduZIDER_sSNHkJQ629f_5-9_DlnXx-xW9Bt3AbXDrftMwfZHjTehZD68i7HGKlxBg7ZUOMMqGkGkuzFcX3uRIemp38BKggA_w</recordid><startdate>20120216</startdate><enddate>20120216</enddate><creator>Lo, Wei-Cheng</creator><creator>Dai, Tian</creator><creator>Liu, Yen-Yi</creator><creator>Wang, Li-Fen</creator><creator>Hwang, Jenn-Kang</creator><creator>Lyu, Ping-Chiang</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20120216</creationdate><title>Deciphering the preference and predicting the viability of circular permutations in proteins</title><author>Lo, Wei-Cheng ; Dai, Tian ; Liu, Yen-Yi ; Wang, Li-Fen ; Hwang, Jenn-Kang ; Lyu, Ping-Chiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c691t-3b0450424228e86eef9a820c6e9b26fb4f22a37cd0864dc580ff45194678b2563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Algorithms</topic><topic>Amino Acid Sequence</topic><topic>Analysis</topic><topic>Artificial intelligence</topic><topic>Artificial neural networks</topic><topic>Back propagation</topic><topic>Biochemistry</topic><topic>Bioinformatics</topic><topic>Biology</topic><topic>Biotechnology</topic><topic>Bonding strength</topic><topic>Chemical bonds</topic><topic>Coiling</topic><topic>Coils</topic><topic>Computer Simulation</topic><topic>Datasets</topic><topic>Dihydrofolate reductase</topic><topic>Enzymes</topic><topic>Forest management</topic><topic>Helices</topic><topic>Hydrogen</topic><topic>Hydrogen bonding</topic><topic>Hydrogen bonds</topic><topic>Hydrophobicity</topic><topic>Learning algorithms</topic><topic>Ligands</topic><topic>Machine learning</topic><topic>Models, Molecular</topic><topic>Molecular biology</topic><topic>Molecular dynamics</topic><topic>Mutagenesis</topic><topic>Neural networks</topic><topic>Permutations</topic><topic>Predictions</topic><topic>Protein Engineering</topic><topic>Protein folding</topic><topic>Proteins</topic><topic>Proteins - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lo, Wei-Cheng</au><au>Dai, Tian</au><au>Liu, Yen-Yi</au><au>Wang, Li-Fen</au><au>Hwang, Jenn-Kang</au><au>Lyu, Ping-Chiang</au><au>Flower, Darren R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Deciphering the preference and predicting the viability of circular permutations in proteins</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2012-02-16</date><risdate>2012</risdate><volume>7</volume><issue>2</issue><spage>e31791</spage><epage>e31791</epage><pages>e31791-e31791</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Circular permutation (CP) refers to situations in which the termini of a protein are relocated to other positions in the structure. CP occurs naturally and has been artificially created to study protein function, stability and folding. Recently CP is increasingly applied to engineer enzyme structure and function, and to create bifunctional fusion proteins unachievable by tandem fusion. CP is a complicated and expensive technique. An intrinsic difficulty in its application lies in the fact that not every position in a protein is amenable for creating a viable permutant. To examine the preferences of CP and develop CP viability prediction methods, we carried out comprehensive analyses of the sequence, structural, and dynamical properties of known CP sites using a variety of statistics and simulation methods, such as the bootstrap aggregating, permutation test and molecular dynamics simulations. CP particularly favors Gly, Pro, Asp and Asn. Positions preferred by CP lie within coils, loops, turns, and at residues that are exposed to solvent, weakly hydrogen-bonded, environmentally unpacked, or flexible. Disfavored positions include Cys, bulky hydrophobic residues, and residues located within helices or near the protein's core. These results fostered the development of an effective viable CP site prediction system, which combined four machine learning methods, e.g., artificial neural networks, the support vector machine, a random forest, and a hierarchical feature integration procedure developed in this work. As assessed by using the hydrofolate reductase dataset as the independent evaluation dataset, this prediction system achieved an AUC of 0.9. Large-scale predictions have been performed for nine thousand representative protein structures; several new potential applications of CP were thus identified. Many unreported preferences of CP are revealed in this study. The developed system is the best CP viability prediction method currently available. This work will facilitate the application of CP in research and biotechnology.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22359629</pmid><doi>10.1371/journal.pone.0031791</doi><tpages>e31791</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Algorithms Amino Acid Sequence Analysis Artificial intelligence Artificial neural networks Back propagation Biochemistry Bioinformatics Biology Biotechnology Bonding strength Chemical bonds Coiling Coils Computer Simulation Datasets Dihydrofolate reductase Enzymes Forest management Helices Hydrogen Hydrogen bonding Hydrogen bonds Hydrophobicity Learning algorithms Ligands Machine learning Models, Molecular Molecular biology Molecular dynamics Mutagenesis Neural networks Permutations Predictions Protein Engineering Protein folding Proteins Proteins - chemistry Reductase Researchers Residues Simulation Software packages Statistical methods Statistical tests Structural stability Structure-function relationships Support Vector Machine Viability |
title | Deciphering the preference and predicting the viability of circular permutations in proteins |
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