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Spontaneous Internalization of Cell Penetrating Peptide-Modified Nanowires into Primary Neurons
Semiconductor nanowire (NW) devices that can address intracellular electrophysiological events with high sensitivity and spatial resolution are emerging as key tools in nanobioelectronics. Intracellular delivery of NWs without compromising cellular integrity and metabolic activity has, however, prov...
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Published in: | Nano letters 2016-02, Vol.16 (2), p.1509-1513 |
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container_title | Nano letters |
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creator | Lee, Jae-Hyun Zhang, Anqi You, Siheng Sean Lieber, Charles M |
description | Semiconductor nanowire (NW) devices that can address intracellular electrophysiological events with high sensitivity and spatial resolution are emerging as key tools in nanobioelectronics. Intracellular delivery of NWs without compromising cellular integrity and metabolic activity has, however, proven difficult without external mechanical forces or electrical pulses. Here, we introduce a biomimetic approach in which a cell penetrating peptide, the trans-activating transcriptional activator (TAT) from human immunodeficiency virus 1, is linked to the surface of Si NWs to facilitate spontaneous internalization of NWs into primary neuronal cells. Confocal microscopy imaging studies at fixed time points demonstrate that TAT-conjugated NWs (TAT-NWs) are fully internalized into mouse hippocampal neurons, and quantitative image analyses reveal an ca. 15% internalization efficiency. In addition, live cell dynamic imaging of NW internalization shows that NW penetration begins within 10–20 min after binding to the membrane and that NWs become fully internalized within 30–40 min. The generality of cell penetrating peptide modification method is further demonstrated by internalization of TAT-NWs into primary dorsal root ganglion (DRG) neurons. |
doi_str_mv | 10.1021/acs.nanolett.6b00020 |
format | article |
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Intracellular delivery of NWs without compromising cellular integrity and metabolic activity has, however, proven difficult without external mechanical forces or electrical pulses. Here, we introduce a biomimetic approach in which a cell penetrating peptide, the trans-activating transcriptional activator (TAT) from human immunodeficiency virus 1, is linked to the surface of Si NWs to facilitate spontaneous internalization of NWs into primary neuronal cells. Confocal microscopy imaging studies at fixed time points demonstrate that TAT-conjugated NWs (TAT-NWs) are fully internalized into mouse hippocampal neurons, and quantitative image analyses reveal an ca. 15% internalization efficiency. In addition, live cell dynamic imaging of NW internalization shows that NW penetration begins within 10–20 min after binding to the membrane and that NWs become fully internalized within 30–40 min. The generality of cell penetrating peptide modification method is further demonstrated by internalization of TAT-NWs into primary dorsal root ganglion (DRG) neurons.</description><identifier>ISSN: 1530-6984</identifier><identifier>EISSN: 1530-6992</identifier><identifier>DOI: 10.1021/acs.nanolett.6b00020</identifier><identifier>PMID: 26745653</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Animals ; Cell-Penetrating Peptides - administration & dosage ; Cell-Penetrating Peptides - chemistry ; Confocal ; Drug Delivery Systems ; Humans ; Imaging ; Mice ; Microscopy, Confocal ; Nanostructure ; Nanowires ; Nanowires - administration & dosage ; Nanowires - chemistry ; Neurons ; Neurons - drug effects ; Neurons - ultrastructure ; Peptides ; Primary Cell Culture ; Semiconductors ; Spontaneous ; tat Gene Products, Human Immunodeficiency Virus - administration & dosage ; tat Gene Products, Human Immunodeficiency Virus - chemistry</subject><ispartof>Nano letters, 2016-02, Vol.16 (2), p.1509-1513</ispartof><rights>Copyright © 2016 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a381t-ab5e528943c69803d56f55a6826029cd6790be810522cc073f91189dc3ff9a8b3</citedby><cites>FETCH-LOGICAL-a381t-ab5e528943c69803d56f55a6826029cd6790be810522cc073f91189dc3ff9a8b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26745653$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Jae-Hyun</creatorcontrib><creatorcontrib>Zhang, Anqi</creatorcontrib><creatorcontrib>You, Siheng Sean</creatorcontrib><creatorcontrib>Lieber, Charles M</creatorcontrib><title>Spontaneous Internalization of Cell Penetrating Peptide-Modified Nanowires into Primary Neurons</title><title>Nano letters</title><addtitle>Nano Lett</addtitle><description>Semiconductor nanowire (NW) devices that can address intracellular electrophysiological events with high sensitivity and spatial resolution are emerging as key tools in nanobioelectronics. Intracellular delivery of NWs without compromising cellular integrity and metabolic activity has, however, proven difficult without external mechanical forces or electrical pulses. Here, we introduce a biomimetic approach in which a cell penetrating peptide, the trans-activating transcriptional activator (TAT) from human immunodeficiency virus 1, is linked to the surface of Si NWs to facilitate spontaneous internalization of NWs into primary neuronal cells. Confocal microscopy imaging studies at fixed time points demonstrate that TAT-conjugated NWs (TAT-NWs) are fully internalized into mouse hippocampal neurons, and quantitative image analyses reveal an ca. 15% internalization efficiency. In addition, live cell dynamic imaging of NW internalization shows that NW penetration begins within 10–20 min after binding to the membrane and that NWs become fully internalized within 30–40 min. The generality of cell penetrating peptide modification method is further demonstrated by internalization of TAT-NWs into primary dorsal root ganglion (DRG) neurons.</description><subject>Animals</subject><subject>Cell-Penetrating Peptides - administration & dosage</subject><subject>Cell-Penetrating Peptides - chemistry</subject><subject>Confocal</subject><subject>Drug Delivery Systems</subject><subject>Humans</subject><subject>Imaging</subject><subject>Mice</subject><subject>Microscopy, Confocal</subject><subject>Nanostructure</subject><subject>Nanowires</subject><subject>Nanowires - administration & dosage</subject><subject>Nanowires - chemistry</subject><subject>Neurons</subject><subject>Neurons - drug effects</subject><subject>Neurons - ultrastructure</subject><subject>Peptides</subject><subject>Primary Cell Culture</subject><subject>Semiconductors</subject><subject>Spontaneous</subject><subject>tat Gene Products, Human Immunodeficiency Virus - administration & dosage</subject><subject>tat Gene Products, Human Immunodeficiency Virus - chemistry</subject><issn>1530-6984</issn><issn>1530-6992</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkVtPxCAQhYnReP8HxvTRl64DFAqPZuNlE2-J-kxoSw2mCyvQGP31sunqoz4xId-ZOTMHoRMMMwwEn-s2zpx2fjApzXgDAAS20D5mFEouJdn-rUW1hw5ifMuIpAx20R7hdcU4o_tIPa28S9oZP8Zi4ZIJTg_2SyfrXeH7Ym6GoXg0zqSQ_9xrrlfJdqa8853tremK--zhwwYTC-uSLx6DXerwWdybMXgXj9BOr4dojjfvIXq5unye35S3D9eL-cVtqanAqdQNM4wIWdE2-wXaMd4zprkgHIhsO15LaIzAwAhpW6hpLzEWsmtp30stGnqIzqa-q-DfRxOTWtrYZvPTagoLEJgQQcj_aM2rGgireUarCW2DjzGYXq2m9RQGtU5B5RTUTwpqk0KWnW4mjM3SdL-in7NnACZgLX_z4_ro8e-e38OZl1k</recordid><startdate>20160210</startdate><enddate>20160210</enddate><creator>Lee, Jae-Hyun</creator><creator>Zhang, Anqi</creator><creator>You, Siheng Sean</creator><creator>Lieber, Charles M</creator><general>American Chemical Society</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>7X8</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20160210</creationdate><title>Spontaneous Internalization of Cell Penetrating Peptide-Modified Nanowires into Primary Neurons</title><author>Lee, Jae-Hyun ; Zhang, Anqi ; You, Siheng Sean ; Lieber, Charles M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a381t-ab5e528943c69803d56f55a6826029cd6790be810522cc073f91189dc3ff9a8b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Cell-Penetrating Peptides - administration & dosage</topic><topic>Cell-Penetrating Peptides - chemistry</topic><topic>Confocal</topic><topic>Drug Delivery Systems</topic><topic>Humans</topic><topic>Imaging</topic><topic>Mice</topic><topic>Microscopy, Confocal</topic><topic>Nanostructure</topic><topic>Nanowires</topic><topic>Nanowires - administration & dosage</topic><topic>Nanowires - chemistry</topic><topic>Neurons</topic><topic>Neurons - drug effects</topic><topic>Neurons - ultrastructure</topic><topic>Peptides</topic><topic>Primary Cell Culture</topic><topic>Semiconductors</topic><topic>Spontaneous</topic><topic>tat Gene Products, Human Immunodeficiency Virus - administration & dosage</topic><topic>tat Gene Products, Human Immunodeficiency Virus - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Jae-Hyun</creatorcontrib><creatorcontrib>Zhang, Anqi</creatorcontrib><creatorcontrib>You, Siheng Sean</creatorcontrib><creatorcontrib>Lieber, Charles M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</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>Nano letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Jae-Hyun</au><au>Zhang, Anqi</au><au>You, Siheng Sean</au><au>Lieber, Charles M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spontaneous Internalization of Cell Penetrating Peptide-Modified Nanowires into Primary Neurons</atitle><jtitle>Nano letters</jtitle><addtitle>Nano Lett</addtitle><date>2016-02-10</date><risdate>2016</risdate><volume>16</volume><issue>2</issue><spage>1509</spage><epage>1513</epage><pages>1509-1513</pages><issn>1530-6984</issn><eissn>1530-6992</eissn><abstract>Semiconductor nanowire (NW) devices that can address intracellular electrophysiological events with high sensitivity and spatial resolution are emerging as key tools in nanobioelectronics. Intracellular delivery of NWs without compromising cellular integrity and metabolic activity has, however, proven difficult without external mechanical forces or electrical pulses. Here, we introduce a biomimetic approach in which a cell penetrating peptide, the trans-activating transcriptional activator (TAT) from human immunodeficiency virus 1, is linked to the surface of Si NWs to facilitate spontaneous internalization of NWs into primary neuronal cells. Confocal microscopy imaging studies at fixed time points demonstrate that TAT-conjugated NWs (TAT-NWs) are fully internalized into mouse hippocampal neurons, and quantitative image analyses reveal an ca. 15% internalization efficiency. In addition, live cell dynamic imaging of NW internalization shows that NW penetration begins within 10–20 min after binding to the membrane and that NWs become fully internalized within 30–40 min. The generality of cell penetrating peptide modification method is further demonstrated by internalization of TAT-NWs into primary dorsal root ganglion (DRG) neurons.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>26745653</pmid><doi>10.1021/acs.nanolett.6b00020</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Cell-Penetrating Peptides - administration & dosage Cell-Penetrating Peptides - chemistry Confocal Drug Delivery Systems Humans Imaging Mice Microscopy, Confocal Nanostructure Nanowires Nanowires - administration & dosage Nanowires - chemistry Neurons Neurons - drug effects Neurons - ultrastructure Peptides Primary Cell Culture Semiconductors Spontaneous tat Gene Products, Human Immunodeficiency Virus - administration & dosage tat Gene Products, Human Immunodeficiency Virus - chemistry |
title | Spontaneous Internalization of Cell Penetrating Peptide-Modified Nanowires into Primary Neurons |
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