Enrichment for RNA Molecules that Bind a Diels-Alder Transition State Analog
RNA molecules that bind a transition state analog for a Diels-Alder reaction (Kd= 0.35 ± 0.05 mM) were isolated from a starting pool of ≈1014sequences by affinity chromatography. After the initial rise and plateau of the amount of RNA that eluted with soluble analog, a step gradient elution was used...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1994-12, Vol.91 (26), p.13028-13032 |
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creator | Morris, Kevin N. Tarasow, Theodore M. Julin, Carol M. Simons, Shauna L. Hilvert, Donald Gold, Larry |
description | RNA molecules that bind a transition state analog for a Diels-Alder reaction (Kd= 0.35 ± 0.05 mM) were isolated from a starting pool of ≈1014sequences by affinity chromatography. After the initial rise and plateau of the amount of RNA that eluted with soluble analog, a step gradient elution was used to further enrich the pool for sequences with higher affinities for the target. To our knowledge, the isolation of RNA molecules that bind either a nonplanar or a hydrophobic ligand has not been reported previously. A conserved nucleotide sequence and secondary structure present in many of the RNA molecules are necessary but not sufficient for binding the analog. No catalysts of the targeted Diels-Alder reaction were found among the binders. The absence of catalysis contrasts with previous successful experiments with antibodies and suggests that other strategies may be needed to identify oligonucleotides with diverse catalytic activities. |
doi_str_mv | 10.1073/pnas.91.26.13028 |
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After the initial rise and plateau of the amount of RNA that eluted with soluble analog, a step gradient elution was used to further enrich the pool for sequences with higher affinities for the target. To our knowledge, the isolation of RNA molecules that bind either a nonplanar or a hydrophobic ligand has not been reported previously. A conserved nucleotide sequence and secondary structure present in many of the RNA molecules are necessary but not sufficient for binding the analog. No catalysts of the targeted Diels-Alder reaction were found among the binders. The absence of catalysis contrasts with previous successful experiments with antibodies and suggests that other strategies may be needed to identify oligonucleotides with diverse catalytic activities.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.91.26.13028</identifier><identifier>PMID: 7528930</identifier><language>eng</language><publisher>United States: National Academy of the Sciences of the United States of America</publisher><subject>Base Sequence ; Catalysis ; Chemistry ; Consensus Sequence ; Conserved sequences ; Diels Alder reactions ; Elution ; Ligands ; Molecular Sequence Data ; Molecules ; Nucleotide sequences ; Nucleotides ; Polymerase chain reaction ; Ribonucleic acid ; RNA ; RNA - chemistry ; Structure-Activity Relationship</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1994-12, Vol.91 (26), p.13028-13032</ispartof><rights>Copyright 1994 The National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Dec 20, 1994</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c525t-9d5f3e03e259dd710867b18c16b976a2cd0fe8a60aea09e2f44d72a0bcaf01933</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/91/26.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/2366477$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/2366477$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7528930$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morris, Kevin N.</creatorcontrib><creatorcontrib>Tarasow, Theodore M.</creatorcontrib><creatorcontrib>Julin, Carol M.</creatorcontrib><creatorcontrib>Simons, Shauna L.</creatorcontrib><creatorcontrib>Hilvert, Donald</creatorcontrib><creatorcontrib>Gold, Larry</creatorcontrib><title>Enrichment for RNA Molecules that Bind a Diels-Alder Transition State Analog</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>RNA molecules that bind a transition state analog for a Diels-Alder reaction (Kd= 0.35 ± 0.05 mM) were isolated from a starting pool of ≈1014sequences by affinity chromatography. After the initial rise and plateau of the amount of RNA that eluted with soluble analog, a step gradient elution was used to further enrich the pool for sequences with higher affinities for the target. To our knowledge, the isolation of RNA molecules that bind either a nonplanar or a hydrophobic ligand has not been reported previously. A conserved nucleotide sequence and secondary structure present in many of the RNA molecules are necessary but not sufficient for binding the analog. No catalysts of the targeted Diels-Alder reaction were found among the binders. The absence of catalysis contrasts with previous successful experiments with antibodies and suggests that other strategies may be needed to identify oligonucleotides with diverse catalytic activities.</description><subject>Base Sequence</subject><subject>Catalysis</subject><subject>Chemistry</subject><subject>Consensus Sequence</subject><subject>Conserved sequences</subject><subject>Diels Alder reactions</subject><subject>Elution</subject><subject>Ligands</subject><subject>Molecular Sequence Data</subject><subject>Molecules</subject><subject>Nucleotide sequences</subject><subject>Nucleotides</subject><subject>Polymerase chain reaction</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA - chemistry</subject><subject>Structure-Activity Relationship</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtvEzEURi1EVUJhzwKExaJiM-H6MfZYYhNKeUgBJChry5nxNBM5dmp7qvLv6zQhKixg5cV3ztX1_RB6RmBKQLI3G2_SVJEpFVPCgDYP0ISAIpXgCh6iCQCVVcMpf4Qep7QCAFU3cIyOZU0bxWCC5uc-Du1ybX3GfYj4-9cZ_hKcbUdnE85Lk_G7wXfY4PeDdamauc5GfBGNT0Megsc_sskWz7xx4fIJOuqNS_bp_j1BPz-cX5x9qubfPn4-m82rtqZ1rlRX98wCs7RWXScJNEIuSNMSsVBSGNp20NvGCDDWgLK057yT1MCiNT0QxdgJerubuxkXa9u1ZflonN7EYW3iLx3MoP9M_LDUl-Fa87qWvOinez2Gq9GmrNdDaq1zxtswJi2FIg3l8F-QCEElKFHAV3-BqzDGcpOkKRDacCZJgWAHtTGkFG1_WJiA3rapt21qRTQV-q7Nory4_9GDsK-v5K_3-db8nd6boPvRuWxvckFf_hstxPMdsUo5xANCmRBcSnYLg7C8rg</recordid><startdate>19941220</startdate><enddate>19941220</enddate><creator>Morris, Kevin N.</creator><creator>Tarasow, Theodore M.</creator><creator>Julin, Carol M.</creator><creator>Simons, Shauna L.</creator><creator>Hilvert, Donald</creator><creator>Gold, Larry</creator><general>National Academy of the Sciences of the United States of America</general><general>National Acad Sciences</general><general>National Academy of Sciences</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19941220</creationdate><title>Enrichment for RNA Molecules that Bind a Diels-Alder Transition State Analog</title><author>Morris, Kevin N. ; Tarasow, Theodore M. ; Julin, Carol M. ; Simons, Shauna L. ; Hilvert, Donald ; Gold, Larry</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c525t-9d5f3e03e259dd710867b18c16b976a2cd0fe8a60aea09e2f44d72a0bcaf01933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Base Sequence</topic><topic>Catalysis</topic><topic>Chemistry</topic><topic>Consensus Sequence</topic><topic>Conserved sequences</topic><topic>Diels Alder reactions</topic><topic>Elution</topic><topic>Ligands</topic><topic>Molecular Sequence Data</topic><topic>Molecules</topic><topic>Nucleotide sequences</topic><topic>Nucleotides</topic><topic>Polymerase chain reaction</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA - chemistry</topic><topic>Structure-Activity Relationship</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morris, Kevin N.</creatorcontrib><creatorcontrib>Tarasow, Theodore M.</creatorcontrib><creatorcontrib>Julin, Carol M.</creatorcontrib><creatorcontrib>Simons, Shauna L.</creatorcontrib><creatorcontrib>Hilvert, Donald</creatorcontrib><creatorcontrib>Gold, Larry</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morris, Kevin N.</au><au>Tarasow, Theodore M.</au><au>Julin, Carol M.</au><au>Simons, Shauna L.</au><au>Hilvert, Donald</au><au>Gold, Larry</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enrichment for RNA Molecules that Bind a Diels-Alder Transition State Analog</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1994-12-20</date><risdate>1994</risdate><volume>91</volume><issue>26</issue><spage>13028</spage><epage>13032</epage><pages>13028-13032</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>RNA molecules that bind a transition state analog for a Diels-Alder reaction (Kd= 0.35 ± 0.05 mM) were isolated from a starting pool of ≈1014sequences by affinity chromatography. After the initial rise and plateau of the amount of RNA that eluted with soluble analog, a step gradient elution was used to further enrich the pool for sequences with higher affinities for the target. To our knowledge, the isolation of RNA molecules that bind either a nonplanar or a hydrophobic ligand has not been reported previously. A conserved nucleotide sequence and secondary structure present in many of the RNA molecules are necessary but not sufficient for binding the analog. No catalysts of the targeted Diels-Alder reaction were found among the binders. The absence of catalysis contrasts with previous successful experiments with antibodies and suggests that other strategies may be needed to identify oligonucleotides with diverse catalytic activities.</abstract><cop>United States</cop><pub>National Academy of the Sciences of the United States of America</pub><pmid>7528930</pmid><doi>10.1073/pnas.91.26.13028</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Base Sequence Catalysis Chemistry Consensus Sequence Conserved sequences Diels Alder reactions Elution Ligands Molecular Sequence Data Molecules Nucleotide sequences Nucleotides Polymerase chain reaction Ribonucleic acid RNA RNA - chemistry Structure-Activity Relationship |
title | Enrichment for RNA Molecules that Bind a Diels-Alder Transition State Analog |
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