Evolutionary selection of personalized melanoma cell/tissue dual-homing peptides for guiding bionanofibers to malignant tumors
Both melanoma cells and tissues were allowed to interact with an identical pool of billions of human-safe phage nanofiber clones with each genetically displaying a unique 12-mer peptide at the tips, respectively, resulting in the discovery of bionanofibers displaying a melanoma cell/tissue dual-homi...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2018-02, Vol.54 (13), p.1631-1634 |
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creator | Yang, Mingying Li, Yan Huai, Yanyan Wang, Chenyuan Yi, Wenfang Mao, Chuanbin |
description | Both melanoma cells and tissues were allowed to interact with an identical pool of billions of human-safe phage nanofiber clones with each genetically displaying a unique 12-mer peptide at the tips, respectively, resulting in the discovery of bionanofibers displaying a melanoma cell/tissue dual-homing peptide for personalized targeted melanoma therapy. |
doi_str_mv | 10.1039/c7cc09077c |
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chemistry</subject><subject>Bacteriophage M13 - metabolism</subject><subject>Cell Line, Tumor</subject><subject>Chlorophyll - analogs & derivatives</subject><subject>Chlorophyll - therapeutic use</subject><subject>Drug Carriers - chemistry</subject><subject>Drug Carriers - metabolism</subject><subject>Drug Carriers - pharmacology</subject><subject>Female</subject><subject>Homing</subject><subject>Humans</subject><subject>Light</subject><subject>Melanocytes - metabolism</subject><subject>Melanoma</subject><subject>Melanoma - metabolism</subject><subject>Melanoma - therapy</subject><subject>Mice, Inbred BALB C</subject><subject>Nanofibers</subject><subject>Nanofibers - chemistry</subject><subject>Peptide Library</subject><subject>Peptides</subject><subject>Peptides - chemistry</subject><subject>Peptides - metabolism</subject><subject>Peptides - pharmacology</subject><subject>Phages</subject><subject>Photochemotherapy - methods</subject><subject>Photosensitizing Agents - therapeutic use</subject><subject>Protein Binding</subject><subject>Tips</subject><subject>Viral Proteins - 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metabolism</topic><topic>Viral Proteins - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Mingying</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Huai, Yanyan</creatorcontrib><creatorcontrib>Wang, Chenyuan</creatorcontrib><creatorcontrib>Yi, Wenfang</creatorcontrib><creatorcontrib>Mao, Chuanbin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</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><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Mingying</au><au>Li, Yan</au><au>Huai, Yanyan</au><au>Wang, Chenyuan</au><au>Yi, Wenfang</au><au>Mao, Chuanbin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evolutionary selection of personalized melanoma cell/tissue dual-homing peptides for guiding bionanofibers to malignant tumors</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2018-02-08</date><risdate>2018</risdate><volume>54</volume><issue>13</issue><spage>1631</spage><epage>1634</epage><pages>1631-1634</pages><issn>1359-7345</issn><issn>1364-548X</issn><eissn>1364-548X</eissn><abstract>Both melanoma cells and tissues were allowed to interact with an identical pool of billions of human-safe phage nanofiber clones with each genetically displaying a unique 12-mer peptide at the tips, respectively, resulting in the discovery of bionanofibers displaying a melanoma cell/tissue dual-homing peptide for personalized targeted melanoma therapy.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>29372921</pmid><doi>10.1039/c7cc09077c</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-8142-3659</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Animals Bacteriophage M13 - chemistry Bacteriophage M13 - metabolism Cell Line, Tumor Chlorophyll - analogs & derivatives Chlorophyll - therapeutic use Drug Carriers - chemistry Drug Carriers - metabolism Drug Carriers - pharmacology Female Homing Humans Light Melanocytes - metabolism Melanoma Melanoma - metabolism Melanoma - therapy Mice, Inbred BALB C Nanofibers Nanofibers - chemistry Peptide Library Peptides Peptides - chemistry Peptides - metabolism Peptides - pharmacology Phages Photochemotherapy - methods Photosensitizing Agents - therapeutic use Protein Binding Tips Viral Proteins - chemistry Viral Proteins - metabolism Viral Proteins - pharmacology |
title | Evolutionary selection of personalized melanoma cell/tissue dual-homing peptides for guiding bionanofibers to malignant tumors |
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