Loading…

Arginine-rich intracellular delivery peptides noncovalently transport protein into living cells

Plasma membranes of plant or animal cells are generally impermeable to peptides or proteins. Many basic peptides have previously been investigated and covalently cross-linked with cargoes for cellular internalization. In the current study, we demonstrate that arginine-rich intracellular delivery (AI...

Full description

Saved in:
Bibliographic Details
Published in:Biochemical and biophysical research communications 2006-08, Vol.346 (3), p.758-767
Main Authors: Wang, Ya-Hui, Chen, Chung-Pin, Chan, Ming-Huan, Chang, Microsugar, Hou, Yu-Wun, Chen, Hwei-Hsien, Hsu, Hui-Ru, Liu, Kevin, Lee, Han-Jung
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c413t-3cc038d7b5fa2ef29a86cacb1ac197fcd30ee02d200a342ac6a1ba6a30da2ffc3
cites cdi_FETCH-LOGICAL-c413t-3cc038d7b5fa2ef29a86cacb1ac197fcd30ee02d200a342ac6a1ba6a30da2ffc3
container_end_page 767
container_issue 3
container_start_page 758
container_title Biochemical and biophysical research communications
container_volume 346
creator Wang, Ya-Hui
Chen, Chung-Pin
Chan, Ming-Huan
Chang, Microsugar
Hou, Yu-Wun
Chen, Hwei-Hsien
Hsu, Hui-Ru
Liu, Kevin
Lee, Han-Jung
description Plasma membranes of plant or animal cells are generally impermeable to peptides or proteins. Many basic peptides have previously been investigated and covalently cross-linked with cargoes for cellular internalization. In the current study, we demonstrate that arginine-rich intracellular delivery (AID) peptides are able to deliver fluorescent proteins or β-galactosidase enzyme into animal and plant cells, as well as animal tissue. Cellular internalization and transdermal delivery of protein could be mediated by effective and nontoxic AID peptides in a neither fusion protein nor conjugation fashion. Therefore, noncovalent AID peptides may provide a useful strategy to have active proteins function in living cells and tissues in vivo.
doi_str_mv 10.1016/j.bbrc.2006.05.205
format article
fullrecord <record><control><sourceid>proquest_osti_</sourceid><recordid>TN_cdi_osti_scitechconnect_20854388</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0006291X06012381</els_id><sourcerecordid>19461623</sourcerecordid><originalsourceid>FETCH-LOGICAL-c413t-3cc038d7b5fa2ef29a86cacb1ac197fcd30ee02d200a342ac6a1ba6a30da2ffc3</originalsourceid><addsrcrecordid>eNp9kEFr3DAQhUVpaTZp_0APwVDozZuRZGtt6CUsbVoI5NJCb0IejRMtXsmRtAv77yuzC7319A7zvcebx9gnDmsOXN3t1sMQcS0A1Braou0btuLQQy04NG_ZCsqlFj3_c8WuU9oBcN6o_j274mrTcaXUiun7-Oy881RHhy-V8zkapGk6TCZWliZ3pHiqZpqzs5QqHzyGo5nI5-lUFdanOcRczTFkcn7xh6qYnH-ulpj0gb0bzZTo40Vv2O_v335tf9SPTw8_t_ePNTZc5loiguzsZmhHI2gUvekUGhy4Qd5vRrQSiEDY8quRjTCoDB-MMhKsEeOI8oZ9PueGlJ1O6DLhCwbvCbMW0LWN7LpCfTlTpe_rgVLWe5eWnsZTOCTN-0ZxJWQBxRnEGFKKNOo5ur2JJ81BL-PrnV7G18v4GtqibTHdXtIPw57sP8tl7QJ8PQNUljg6iktR8kjWxaWnDe5_-X8BA7yYwg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19461623</pqid></control><display><type>article</type><title>Arginine-rich intracellular delivery peptides noncovalently transport protein into living cells</title><source>Elsevier</source><creator>Wang, Ya-Hui ; Chen, Chung-Pin ; Chan, Ming-Huan ; Chang, Microsugar ; Hou, Yu-Wun ; Chen, Hwei-Hsien ; Hsu, Hui-Ru ; Liu, Kevin ; Lee, Han-Jung</creator><creatorcontrib>Wang, Ya-Hui ; Chen, Chung-Pin ; Chan, Ming-Huan ; Chang, Microsugar ; Hou, Yu-Wun ; Chen, Hwei-Hsien ; Hsu, Hui-Ru ; Liu, Kevin ; Lee, Han-Jung</creatorcontrib><description>Plasma membranes of plant or animal cells are generally impermeable to peptides or proteins. Many basic peptides have previously been investigated and covalently cross-linked with cargoes for cellular internalization. In the current study, we demonstrate that arginine-rich intracellular delivery (AID) peptides are able to deliver fluorescent proteins or β-galactosidase enzyme into animal and plant cells, as well as animal tissue. Cellular internalization and transdermal delivery of protein could be mediated by effective and nontoxic AID peptides in a neither fusion protein nor conjugation fashion. Therefore, noncovalent AID peptides may provide a useful strategy to have active proteins function in living cells and tissues in vivo.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2006.05.205</identifier><identifier>PMID: 16781666</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>60 APPLIED LIFE SCIENCES ; ANIMAL CELLS ; ANIMAL TISSUES ; Animals ; ARGININE ; Arginine - metabolism ; Cell Line ; Cell Line, Tumor ; Cell penetrating peptide ; Cell Survival ; Cells - cytology ; Cells - metabolism ; Cellular internalization ; Cricetinae ; GALACTOSIDASE ; Green fluorescent protein ; Humans ; IN VIVO ; Liver - cytology ; Liver - metabolism ; Mice ; Onions - cytology ; Onions - metabolism ; PEPTIDES ; Peptides - chemistry ; Peptides - genetics ; Peptides - metabolism ; Peptides - toxicity ; PLANT CELLS ; Plasmids - genetics ; Protein transduction domain ; Protein Transport ; Skin - cytology ; Skin - metabolism ; Transdermal delivery</subject><ispartof>Biochemical and biophysical research communications, 2006-08, Vol.346 (3), p.758-767</ispartof><rights>2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c413t-3cc038d7b5fa2ef29a86cacb1ac197fcd30ee02d200a342ac6a1ba6a30da2ffc3</citedby><cites>FETCH-LOGICAL-c413t-3cc038d7b5fa2ef29a86cacb1ac197fcd30ee02d200a342ac6a1ba6a30da2ffc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16781666$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/20854388$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Ya-Hui</creatorcontrib><creatorcontrib>Chen, Chung-Pin</creatorcontrib><creatorcontrib>Chan, Ming-Huan</creatorcontrib><creatorcontrib>Chang, Microsugar</creatorcontrib><creatorcontrib>Hou, Yu-Wun</creatorcontrib><creatorcontrib>Chen, Hwei-Hsien</creatorcontrib><creatorcontrib>Hsu, Hui-Ru</creatorcontrib><creatorcontrib>Liu, Kevin</creatorcontrib><creatorcontrib>Lee, Han-Jung</creatorcontrib><title>Arginine-rich intracellular delivery peptides noncovalently transport protein into living cells</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Plasma membranes of plant or animal cells are generally impermeable to peptides or proteins. Many basic peptides have previously been investigated and covalently cross-linked with cargoes for cellular internalization. In the current study, we demonstrate that arginine-rich intracellular delivery (AID) peptides are able to deliver fluorescent proteins or β-galactosidase enzyme into animal and plant cells, as well as animal tissue. Cellular internalization and transdermal delivery of protein could be mediated by effective and nontoxic AID peptides in a neither fusion protein nor conjugation fashion. Therefore, noncovalent AID peptides may provide a useful strategy to have active proteins function in living cells and tissues in vivo.</description><subject>60 APPLIED LIFE SCIENCES</subject><subject>ANIMAL CELLS</subject><subject>ANIMAL TISSUES</subject><subject>Animals</subject><subject>ARGININE</subject><subject>Arginine - metabolism</subject><subject>Cell Line</subject><subject>Cell Line, Tumor</subject><subject>Cell penetrating peptide</subject><subject>Cell Survival</subject><subject>Cells - cytology</subject><subject>Cells - metabolism</subject><subject>Cellular internalization</subject><subject>Cricetinae</subject><subject>GALACTOSIDASE</subject><subject>Green fluorescent protein</subject><subject>Humans</subject><subject>IN VIVO</subject><subject>Liver - cytology</subject><subject>Liver - metabolism</subject><subject>Mice</subject><subject>Onions - cytology</subject><subject>Onions - metabolism</subject><subject>PEPTIDES</subject><subject>Peptides - chemistry</subject><subject>Peptides - genetics</subject><subject>Peptides - metabolism</subject><subject>Peptides - toxicity</subject><subject>PLANT CELLS</subject><subject>Plasmids - genetics</subject><subject>Protein transduction domain</subject><subject>Protein Transport</subject><subject>Skin - cytology</subject><subject>Skin - metabolism</subject><subject>Transdermal delivery</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp9kEFr3DAQhUVpaTZp_0APwVDozZuRZGtt6CUsbVoI5NJCb0IejRMtXsmRtAv77yuzC7319A7zvcebx9gnDmsOXN3t1sMQcS0A1Braou0btuLQQy04NG_ZCsqlFj3_c8WuU9oBcN6o_j274mrTcaXUiun7-Oy881RHhy-V8zkapGk6TCZWliZ3pHiqZpqzs5QqHzyGo5nI5-lUFdanOcRczTFkcn7xh6qYnH-ulpj0gb0bzZTo40Vv2O_v335tf9SPTw8_t_ePNTZc5loiguzsZmhHI2gUvekUGhy4Qd5vRrQSiEDY8quRjTCoDB-MMhKsEeOI8oZ9PueGlJ1O6DLhCwbvCbMW0LWN7LpCfTlTpe_rgVLWe5eWnsZTOCTN-0ZxJWQBxRnEGFKKNOo5ur2JJ81BL-PrnV7G18v4GtqibTHdXtIPw57sP8tl7QJ8PQNUljg6iktR8kjWxaWnDe5_-X8BA7yYwg</recordid><startdate>20060804</startdate><enddate>20060804</enddate><creator>Wang, Ya-Hui</creator><creator>Chen, Chung-Pin</creator><creator>Chan, Ming-Huan</creator><creator>Chang, Microsugar</creator><creator>Hou, Yu-Wun</creator><creator>Chen, Hwei-Hsien</creator><creator>Hsu, Hui-Ru</creator><creator>Liu, Kevin</creator><creator>Lee, Han-Jung</creator><general>Elsevier Inc</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>OTOTI</scope></search><sort><creationdate>20060804</creationdate><title>Arginine-rich intracellular delivery peptides noncovalently transport protein into living cells</title><author>Wang, Ya-Hui ; Chen, Chung-Pin ; Chan, Ming-Huan ; Chang, Microsugar ; Hou, Yu-Wun ; Chen, Hwei-Hsien ; Hsu, Hui-Ru ; Liu, Kevin ; Lee, Han-Jung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-3cc038d7b5fa2ef29a86cacb1ac197fcd30ee02d200a342ac6a1ba6a30da2ffc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>60 APPLIED LIFE SCIENCES</topic><topic>ANIMAL CELLS</topic><topic>ANIMAL TISSUES</topic><topic>Animals</topic><topic>ARGININE</topic><topic>Arginine - metabolism</topic><topic>Cell Line</topic><topic>Cell Line, Tumor</topic><topic>Cell penetrating peptide</topic><topic>Cell Survival</topic><topic>Cells - cytology</topic><topic>Cells - metabolism</topic><topic>Cellular internalization</topic><topic>Cricetinae</topic><topic>GALACTOSIDASE</topic><topic>Green fluorescent protein</topic><topic>Humans</topic><topic>IN VIVO</topic><topic>Liver - cytology</topic><topic>Liver - metabolism</topic><topic>Mice</topic><topic>Onions - cytology</topic><topic>Onions - metabolism</topic><topic>PEPTIDES</topic><topic>Peptides - chemistry</topic><topic>Peptides - genetics</topic><topic>Peptides - metabolism</topic><topic>Peptides - toxicity</topic><topic>PLANT CELLS</topic><topic>Plasmids - genetics</topic><topic>Protein transduction domain</topic><topic>Protein Transport</topic><topic>Skin - cytology</topic><topic>Skin - metabolism</topic><topic>Transdermal delivery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Ya-Hui</creatorcontrib><creatorcontrib>Chen, Chung-Pin</creatorcontrib><creatorcontrib>Chan, Ming-Huan</creatorcontrib><creatorcontrib>Chang, Microsugar</creatorcontrib><creatorcontrib>Hou, Yu-Wun</creatorcontrib><creatorcontrib>Chen, Hwei-Hsien</creatorcontrib><creatorcontrib>Hsu, Hui-Ru</creatorcontrib><creatorcontrib>Liu, Kevin</creatorcontrib><creatorcontrib>Lee, Han-Jung</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>OSTI.GOV</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Ya-Hui</au><au>Chen, Chung-Pin</au><au>Chan, Ming-Huan</au><au>Chang, Microsugar</au><au>Hou, Yu-Wun</au><au>Chen, Hwei-Hsien</au><au>Hsu, Hui-Ru</au><au>Liu, Kevin</au><au>Lee, Han-Jung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Arginine-rich intracellular delivery peptides noncovalently transport protein into living cells</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2006-08-04</date><risdate>2006</risdate><volume>346</volume><issue>3</issue><spage>758</spage><epage>767</epage><pages>758-767</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Plasma membranes of plant or animal cells are generally impermeable to peptides or proteins. Many basic peptides have previously been investigated and covalently cross-linked with cargoes for cellular internalization. In the current study, we demonstrate that arginine-rich intracellular delivery (AID) peptides are able to deliver fluorescent proteins or β-galactosidase enzyme into animal and plant cells, as well as animal tissue. Cellular internalization and transdermal delivery of protein could be mediated by effective and nontoxic AID peptides in a neither fusion protein nor conjugation fashion. Therefore, noncovalent AID peptides may provide a useful strategy to have active proteins function in living cells and tissues in vivo.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16781666</pmid><doi>10.1016/j.bbrc.2006.05.205</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0006-291X
ispartof Biochemical and biophysical research communications, 2006-08, Vol.346 (3), p.758-767
issn 0006-291X
1090-2104
language eng
recordid cdi_osti_scitechconnect_20854388
source Elsevier
subjects 60 APPLIED LIFE SCIENCES
ANIMAL CELLS
ANIMAL TISSUES
Animals
ARGININE
Arginine - metabolism
Cell Line
Cell Line, Tumor
Cell penetrating peptide
Cell Survival
Cells - cytology
Cells - metabolism
Cellular internalization
Cricetinae
GALACTOSIDASE
Green fluorescent protein
Humans
IN VIVO
Liver - cytology
Liver - metabolism
Mice
Onions - cytology
Onions - metabolism
PEPTIDES
Peptides - chemistry
Peptides - genetics
Peptides - metabolism
Peptides - toxicity
PLANT CELLS
Plasmids - genetics
Protein transduction domain
Protein Transport
Skin - cytology
Skin - metabolism
Transdermal delivery
title Arginine-rich intracellular delivery peptides noncovalently transport protein into living cells
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T21%3A07%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_osti_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Arginine-rich%20intracellular%20delivery%20peptides%20noncovalently%20transport%20protein%20into%20living%20cells&rft.jtitle=Biochemical%20and%20biophysical%20research%20communications&rft.au=Wang,%20Ya-Hui&rft.date=2006-08-04&rft.volume=346&rft.issue=3&rft.spage=758&rft.epage=767&rft.pages=758-767&rft.issn=0006-291X&rft.eissn=1090-2104&rft_id=info:doi/10.1016/j.bbrc.2006.05.205&rft_dat=%3Cproquest_osti_%3E19461623%3C/proquest_osti_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c413t-3cc038d7b5fa2ef29a86cacb1ac197fcd30ee02d200a342ac6a1ba6a30da2ffc3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=19461623&rft_id=info:pmid/16781666&rfr_iscdi=true