DNA binding fluorescent proteins for the direct visualization of large DNA molecules
Fluorescent proteins that also bind DNA molecules are useful reagents for a broad range of biological applications because they can be optically localized and tracked within cells, or provide versatile labels for in vitro experiments. We report a novel design for a fluorescent, DNA-binding protein (...
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Veröffentlicht in: | Nucleic acids research 2016-01, Vol.44 (1), p.e6-e6 |
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container_title | Nucleic acids research |
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creator | Lee, Seonghyun Oh, Yeeun Lee, Jungyoon Choe, Sojeong Lim, Sangyong Lee, Hyun Soo Jo, Kyubong Schwartz, David C |
description | Fluorescent proteins that also bind DNA molecules are useful reagents for a broad range of biological applications because they can be optically localized and tracked within cells, or provide versatile labels for in vitro experiments. We report a novel design for a fluorescent, DNA-binding protein (FP-DBP) that completely 'paints' entire DNA molecules, whereby sequence-independent DNA binding is accomplished by linking a fluorescent protein to two small peptides (KWKWKKA) using lysine for binding to the DNA phosphates, and tryptophan for intercalating between DNA bases. Importantly, this ubiquitous binding motif enables fluorescent proteins (Kd = 14.7 μM) to confluently stain DNA molecules and such binding is reversible via pH shifts. These proteins offer useful robust advantages for single DNA molecule studies: lack of fluorophore mediated photocleavage and staining that does not perturb polymer contour lengths. Accordingly, we demonstrate confluent staining of naked DNA molecules presented within microfluidic devices, or localized within live bacterial cells. |
doi_str_mv | 10.1093/nar/gkv834 |
format | Article |
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We report a novel design for a fluorescent, DNA-binding protein (FP-DBP) that completely 'paints' entire DNA molecules, whereby sequence-independent DNA binding is accomplished by linking a fluorescent protein to two small peptides (KWKWKKA) using lysine for binding to the DNA phosphates, and tryptophan for intercalating between DNA bases. Importantly, this ubiquitous binding motif enables fluorescent proteins (Kd = 14.7 μM) to confluently stain DNA molecules and such binding is reversible via pH shifts. These proteins offer useful robust advantages for single DNA molecule studies: lack of fluorophore mediated photocleavage and staining that does not perturb polymer contour lengths. Accordingly, we demonstrate confluent staining of naked DNA molecules presented within microfluidic devices, or localized within live bacterial cells.</description><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/gkv834</identifier><identifier>PMID: 26264666</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>DNA - metabolism ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; Escherichia coli - genetics ; Escherichia coli - metabolism ; Humans ; Luminescent Proteins - genetics ; Luminescent Proteins - metabolism ; Methods Online ; Microscopy, Fluorescence ; Molecular Imaging - methods ; Recombinant Fusion Proteins</subject><ispartof>Nucleic acids research, 2016-01, Vol.44 (1), p.e6-e6</ispartof><rights>The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research.</rights><rights>The Author(s) 2015. 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We report a novel design for a fluorescent, DNA-binding protein (FP-DBP) that completely 'paints' entire DNA molecules, whereby sequence-independent DNA binding is accomplished by linking a fluorescent protein to two small peptides (KWKWKKA) using lysine for binding to the DNA phosphates, and tryptophan for intercalating between DNA bases. Importantly, this ubiquitous binding motif enables fluorescent proteins (Kd = 14.7 μM) to confluently stain DNA molecules and such binding is reversible via pH shifts. These proteins offer useful robust advantages for single DNA molecule studies: lack of fluorophore mediated photocleavage and staining that does not perturb polymer contour lengths. Accordingly, we demonstrate confluent staining of naked DNA molecules presented within microfluidic devices, or localized within live bacterial cells.</description><subject>DNA - metabolism</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - metabolism</subject><subject>Humans</subject><subject>Luminescent Proteins - genetics</subject><subject>Luminescent Proteins - metabolism</subject><subject>Methods Online</subject><subject>Microscopy, Fluorescence</subject><subject>Molecular Imaging - methods</subject><subject>Recombinant Fusion Proteins</subject><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkD1PwzAQhi0EoqWw8AOQR5ZQ23Eu9oJU8S1VsJQ5chI7NbhxsZNK8OtJRUGwMd1J9-jRey9Cp5RcUCLTaavCtHndiJTvoTFNgSVcAttHY5KSLKGEixE6ivGFEMppxg_RiAEDDgBjtLh-nOHStrVtG2xc74OOlW47vA6-07aN2PiAu6XGtQ266vDGxl45-6E661vsDXYqNBpvNSvvdNU7HY_RgVEu6pPdnKDn25vF1X0yf7p7uJrNkzVjsks0N8wAiJKLOsu4JBpYVg27NHmeaiFlbbihTOWgVVoqUECqssoM5JyKAZmgyy_vui9Xut7mDsoV62BXKrwXXtni76W1y6Lxm4LnJAPBB8H5ThD8W69jV6zs8L5zqtW-jwXNJZGcCEH_gcLAQU626NnvWD95vltPPwEWVoUS</recordid><startdate>20160108</startdate><enddate>20160108</enddate><creator>Lee, Seonghyun</creator><creator>Oh, Yeeun</creator><creator>Lee, Jungyoon</creator><creator>Choe, Sojeong</creator><creator>Lim, Sangyong</creator><creator>Lee, Hyun Soo</creator><creator>Jo, Kyubong</creator><creator>Schwartz, David C</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20160108</creationdate><title>DNA binding fluorescent proteins for the direct visualization of large DNA molecules</title><author>Lee, Seonghyun ; Oh, Yeeun ; Lee, Jungyoon ; Choe, Sojeong ; Lim, Sangyong ; Lee, Hyun Soo ; Jo, Kyubong ; Schwartz, David C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p229t-e4f2f668b48d55490e625c8d59f773e899df4f12a76ea3ba6a60cbc5f67418773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>DNA - metabolism</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - metabolism</topic><topic>Humans</topic><topic>Luminescent Proteins - genetics</topic><topic>Luminescent Proteins - metabolism</topic><topic>Methods Online</topic><topic>Microscopy, Fluorescence</topic><topic>Molecular Imaging - methods</topic><topic>Recombinant Fusion Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Seonghyun</creatorcontrib><creatorcontrib>Oh, Yeeun</creatorcontrib><creatorcontrib>Lee, Jungyoon</creatorcontrib><creatorcontrib>Choe, Sojeong</creatorcontrib><creatorcontrib>Lim, Sangyong</creatorcontrib><creatorcontrib>Lee, Hyun Soo</creatorcontrib><creatorcontrib>Jo, Kyubong</creatorcontrib><creatorcontrib>Schwartz, David C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Seonghyun</au><au>Oh, Yeeun</au><au>Lee, Jungyoon</au><au>Choe, Sojeong</au><au>Lim, Sangyong</au><au>Lee, Hyun Soo</au><au>Jo, Kyubong</au><au>Schwartz, David C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DNA binding fluorescent proteins for the direct visualization of large DNA molecules</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2016-01-08</date><risdate>2016</risdate><volume>44</volume><issue>1</issue><spage>e6</spage><epage>e6</epage><pages>e6-e6</pages><issn>0305-1048</issn><eissn>1362-4962</eissn><abstract>Fluorescent proteins that also bind DNA molecules are useful reagents for a broad range of biological applications because they can be optically localized and tracked within cells, or provide versatile labels for in vitro experiments. We report a novel design for a fluorescent, DNA-binding protein (FP-DBP) that completely 'paints' entire DNA molecules, whereby sequence-independent DNA binding is accomplished by linking a fluorescent protein to two small peptides (KWKWKKA) using lysine for binding to the DNA phosphates, and tryptophan for intercalating between DNA bases. Importantly, this ubiquitous binding motif enables fluorescent proteins (Kd = 14.7 μM) to confluently stain DNA molecules and such binding is reversible via pH shifts. These proteins offer useful robust advantages for single DNA molecule studies: lack of fluorophore mediated photocleavage and staining that does not perturb polymer contour lengths. Accordingly, we demonstrate confluent staining of naked DNA molecules presented within microfluidic devices, or localized within live bacterial cells.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>26264666</pmid><doi>10.1093/nar/gkv834</doi><oa>free_for_read</oa></addata></record> |
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subjects | DNA - metabolism DNA-Binding Proteins - genetics DNA-Binding Proteins - metabolism Escherichia coli - genetics Escherichia coli - metabolism Humans Luminescent Proteins - genetics Luminescent Proteins - metabolism Methods Online Microscopy, Fluorescence Molecular Imaging - methods Recombinant Fusion Proteins |
title | DNA binding fluorescent proteins for the direct visualization of large DNA molecules |
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