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Engineering of Vault Nanocapsules with Enzymatic and Fluorescent Properties
One of the central issues facing the emerging field of nanotechnology is cellular compatibility. Nanoparticles have been proposed for diagnostic and therapeutic applications, including drug delivery, gene therapy, biological sensors, and controlled catalysis. Viruses, liposomes, peptides, and synthe...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2005-03, Vol.102 (12), p.4348-4352 |
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creator | Kickhoefer, Valerie A. Garcia, Yvette Mikyas, Yeshi Johansson, Erik Zhou, Jing C. Raval-Fernandes, Sujna Minoofar, Payam Zink, Jeffrey I. Dunn, Bruce Stewart, Phoebe L. Rome, Leonard H. Hawthorne, M. Frederick |
description | One of the central issues facing the emerging field of nanotechnology is cellular compatibility. Nanoparticles have been proposed for diagnostic and therapeutic applications, including drug delivery, gene therapy, biological sensors, and controlled catalysis. Viruses, liposomes, peptides, and synthetic and natural polymers have been engineered for these applications, yet significant limitations continue to prevent their use. Avoidance of the body's natural immune system, lack of targeting specificity, and the inability to control packaging and release are remaining obstacles. We have explored the use of a naturally occurring cellular nanoparticle known as the vault, which is named for its morphology with multiple arches reminiscent of cathedral ceilings. Vaults are 13-MDa ribonucleoprotein particles with an internal cavity large enough to sequester hundreds of proteins. Here, we report a strategy to target and sequester biologically active materials within the vault cavity. Attachment of a vault-targeting peptide to two proteins, luciferase and a variant of GFP, resulted in their sequestration within the vault cavity. The targeted proteins confer enzymatic and fluorescent properties on the recombinant vaults, both of which can be detected by their emission of light. The modified vaults are compatible with living cells. The ability to engineer vault particles with designed properties and functionalities represents an important step toward development of a biocompatible nanocapsule. |
doi_str_mv | 10.1073/pnas.0500929102 |
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We have explored the use of a naturally occurring cellular nanoparticle known as the vault, which is named for its morphology with multiple arches reminiscent of cathedral ceilings. Vaults are 13-MDa ribonucleoprotein particles with an internal cavity large enough to sequester hundreds of proteins. Here, we report a strategy to target and sequester biologically active materials within the vault cavity. Attachment of a vault-targeting peptide to two proteins, luciferase and a variant of GFP, resulted in their sequestration within the vault cavity. The targeted proteins confer enzymatic and fluorescent properties on the recombinant vaults, both of which can be detected by their emission of light. The modified vaults are compatible with living cells. The ability to engineer vault particles with designed properties and functionalities represents an important step toward development of a biocompatible nanocapsule.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.0500929102</identifier><identifier>PMID: 15753293</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Biological Sciences ; Biological Transport, Active ; Cryoelectron Microscopy ; Enzymes ; Fluorescence ; Fluorescent Dyes - chemistry ; Fluorescent Dyes - metabolism ; Green Fluorescent Proteins - chemistry ; Green Fluorescent Proteins - genetics ; Green Fluorescent Proteins - metabolism ; Green Fluorescent Proteins - ultrastructure ; HeLa Cells ; Humans ; Image Processing, Computer-Assisted ; In Vitro Techniques ; Luciferases - chemistry ; Luciferases - genetics ; Luciferases - metabolism ; Materials science ; Mitral valve prolapse ; Models, Molecular ; Molecular Conformation ; Molecules ; Nanostructures - chemistry ; Nanostructures - ultrastructure ; Nanotechnology ; Protein Engineering ; Proteins ; Recombinant Fusion Proteins - chemistry ; Recombinant Fusion Proteins - genetics ; Recombinant Fusion Proteins - metabolism ; Recombinant Fusion Proteins - ultrastructure ; Time dependence ; Vault ribonucleoprotein particles ; Vault Ribonucleoprotein Particles - chemistry ; Vault Ribonucleoprotein Particles - genetics ; Vault Ribonucleoprotein Particles - metabolism ; Vault Ribonucleoprotein Particles - ultrastructure</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2005-03, Vol.102 (12), p.4348-4352</ispartof><rights>Copyright 1993/2005 The National Academy of Sciences of the United States of America</rights><rights>Copyright © 2005, The National Academy of Sciences 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c491t-b13e70cdce395d76370cc2082348c44dbfc33facee4d55c37ca3a10214f4ebed3</citedby><cites>FETCH-LOGICAL-c491t-b13e70cdce395d76370cc2082348c44dbfc33facee4d55c37ca3a10214f4ebed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/102/12.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3374984$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3374984$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15753293$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kickhoefer, Valerie A.</creatorcontrib><creatorcontrib>Garcia, Yvette</creatorcontrib><creatorcontrib>Mikyas, Yeshi</creatorcontrib><creatorcontrib>Johansson, Erik</creatorcontrib><creatorcontrib>Zhou, Jing C.</creatorcontrib><creatorcontrib>Raval-Fernandes, Sujna</creatorcontrib><creatorcontrib>Minoofar, Payam</creatorcontrib><creatorcontrib>Zink, Jeffrey I.</creatorcontrib><creatorcontrib>Dunn, Bruce</creatorcontrib><creatorcontrib>Stewart, Phoebe L.</creatorcontrib><creatorcontrib>Rome, Leonard H.</creatorcontrib><creatorcontrib>Hawthorne, M. Frederick</creatorcontrib><title>Engineering of Vault Nanocapsules with Enzymatic and Fluorescent Properties</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>One of the central issues facing the emerging field of nanotechnology is cellular compatibility. Nanoparticles have been proposed for diagnostic and therapeutic applications, including drug delivery, gene therapy, biological sensors, and controlled catalysis. Viruses, liposomes, peptides, and synthetic and natural polymers have been engineered for these applications, yet significant limitations continue to prevent their use. Avoidance of the body's natural immune system, lack of targeting specificity, and the inability to control packaging and release are remaining obstacles. We have explored the use of a naturally occurring cellular nanoparticle known as the vault, which is named for its morphology with multiple arches reminiscent of cathedral ceilings. Vaults are 13-MDa ribonucleoprotein particles with an internal cavity large enough to sequester hundreds of proteins. Here, we report a strategy to target and sequester biologically active materials within the vault cavity. Attachment of a vault-targeting peptide to two proteins, luciferase and a variant of GFP, resulted in their sequestration within the vault cavity. The targeted proteins confer enzymatic and fluorescent properties on the recombinant vaults, both of which can be detected by their emission of light. The modified vaults are compatible with living cells. The ability to engineer vault particles with designed properties and functionalities represents an important step toward development of a biocompatible nanocapsule.</description><subject>Biological Sciences</subject><subject>Biological Transport, Active</subject><subject>Cryoelectron Microscopy</subject><subject>Enzymes</subject><subject>Fluorescence</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Fluorescent Dyes - metabolism</subject><subject>Green Fluorescent Proteins - chemistry</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Green Fluorescent Proteins - ultrastructure</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>In Vitro Techniques</subject><subject>Luciferases - chemistry</subject><subject>Luciferases - genetics</subject><subject>Luciferases - metabolism</subject><subject>Materials science</subject><subject>Mitral valve prolapse</subject><subject>Models, Molecular</subject><subject>Molecular Conformation</subject><subject>Molecules</subject><subject>Nanostructures - chemistry</subject><subject>Nanostructures - ultrastructure</subject><subject>Nanotechnology</subject><subject>Protein Engineering</subject><subject>Proteins</subject><subject>Recombinant Fusion Proteins - chemistry</subject><subject>Recombinant Fusion Proteins - genetics</subject><subject>Recombinant Fusion Proteins - metabolism</subject><subject>Recombinant Fusion Proteins - ultrastructure</subject><subject>Time dependence</subject><subject>Vault ribonucleoprotein particles</subject><subject>Vault Ribonucleoprotein Particles - chemistry</subject><subject>Vault Ribonucleoprotein Particles - genetics</subject><subject>Vault Ribonucleoprotein Particles - metabolism</subject><subject>Vault Ribonucleoprotein Particles - ultrastructure</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqNkb1vFDEUxC0EIsdBTYNgqyjNJv5crwsKFF0ISgQUQGv5vG8vjvbsje2FhL8en-6UIw3BjWX5N09vZhB6TfAxwZKdjN6kYywwVlQRTJ-gGcGK1A1X-CmaYUxl3XLKD9CLlK5xwUSLn6MDIqRgVLEZulj4lfMA0flVFfrqh5mGXH02PlgzpmmAVP1y-apa-N93a5OdrYzvqrNhChGSBZ-rrzGMELOD9BI9682Q4NXunqPvZ4tvp-f15ZePn04_XNaWK5LrJWEgse0sMCU62bDysBS3lPHWct4te8tYbywA74SwTFrDTDFHeM9hCR2bo_fbueO0XEO32SKaQY_RrU2808E4_fDHuyu9Cj-1KIeRoj_c6WO4mSBlvXbFyzAYD2FKupGCN6x5HKRKciXV_4CcUELEoyCRLRaiRDFHJ1vQxpBShP7eHsF6U73eVK_31RfF279T2fO7rgtwtAM2yv04qgnVvISv-2kYMtzmgr77N1qIN1viOuUQ7xHGSiItZ38AYJHNjQ</recordid><startdate>20050322</startdate><enddate>20050322</enddate><creator>Kickhoefer, Valerie A.</creator><creator>Garcia, Yvette</creator><creator>Mikyas, Yeshi</creator><creator>Johansson, Erik</creator><creator>Zhou, Jing C.</creator><creator>Raval-Fernandes, Sujna</creator><creator>Minoofar, Payam</creator><creator>Zink, Jeffrey I.</creator><creator>Dunn, Bruce</creator><creator>Stewart, Phoebe L.</creator><creator>Rome, Leonard H.</creator><creator>Hawthorne, M. 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Frederick</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Engineering of Vault Nanocapsules with Enzymatic and Fluorescent Properties</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2005-03-22</date><risdate>2005</risdate><volume>102</volume><issue>12</issue><spage>4348</spage><epage>4352</epage><pages>4348-4352</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>One of the central issues facing the emerging field of nanotechnology is cellular compatibility. Nanoparticles have been proposed for diagnostic and therapeutic applications, including drug delivery, gene therapy, biological sensors, and controlled catalysis. Viruses, liposomes, peptides, and synthetic and natural polymers have been engineered for these applications, yet significant limitations continue to prevent their use. Avoidance of the body's natural immune system, lack of targeting specificity, and the inability to control packaging and release are remaining obstacles. We have explored the use of a naturally occurring cellular nanoparticle known as the vault, which is named for its morphology with multiple arches reminiscent of cathedral ceilings. Vaults are 13-MDa ribonucleoprotein particles with an internal cavity large enough to sequester hundreds of proteins. Here, we report a strategy to target and sequester biologically active materials within the vault cavity. Attachment of a vault-targeting peptide to two proteins, luciferase and a variant of GFP, resulted in their sequestration within the vault cavity. The targeted proteins confer enzymatic and fluorescent properties on the recombinant vaults, both of which can be detected by their emission of light. The modified vaults are compatible with living cells. The ability to engineer vault particles with designed properties and functionalities represents an important step toward development of a biocompatible nanocapsule.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>15753293</pmid><doi>10.1073/pnas.0500929102</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological Sciences Biological Transport, Active Cryoelectron Microscopy Enzymes Fluorescence Fluorescent Dyes - chemistry Fluorescent Dyes - metabolism Green Fluorescent Proteins - chemistry Green Fluorescent Proteins - genetics Green Fluorescent Proteins - metabolism Green Fluorescent Proteins - ultrastructure HeLa Cells Humans Image Processing, Computer-Assisted In Vitro Techniques Luciferases - chemistry Luciferases - genetics Luciferases - metabolism Materials science Mitral valve prolapse Models, Molecular Molecular Conformation Molecules Nanostructures - chemistry Nanostructures - ultrastructure Nanotechnology Protein Engineering Proteins Recombinant Fusion Proteins - chemistry Recombinant Fusion Proteins - genetics Recombinant Fusion Proteins - metabolism Recombinant Fusion Proteins - ultrastructure Time dependence Vault ribonucleoprotein particles Vault Ribonucleoprotein Particles - chemistry Vault Ribonucleoprotein Particles - genetics Vault Ribonucleoprotein Particles - metabolism Vault Ribonucleoprotein Particles - ultrastructure |
title | Engineering of Vault Nanocapsules with Enzymatic and Fluorescent Properties |
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