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A drug release switch based on protein-inhibitor supramolecular interaction
In this report, we describe a new system in which mesoporous silica nanoparticles (MSNs) are gated with α-chymotrypsin A protein (CTRA) and the cargoes within the vehicles are released in the presence of phenylmethanesulfonyl fluoride (PMSF), a canonical inhibitor of CTRA. This cargo release switch...
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Published in: | RSC advances 2016-01, Vol.6 (3), p.2548-25484 |
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container_title | RSC advances |
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creator | Wang, Xiaoliang Liu, Pengchang Chen, Zhijun Shen, Jiacong |
description | In this report, we describe a new system in which mesoporous silica nanoparticles (MSNs) are gated with α-chymotrypsin A protein (CTRA) and the cargoes within the vehicles are released in the presence of phenylmethanesulfonyl fluoride (PMSF), a canonical inhibitor of CTRA. This cargo release switch is based on the specific interaction between CTRA and PMSF as well as structural changes upon their supramolecular complex formation. This host-guest gating system works smoothly both
in vitro
and within cells. This type of bio-switch may be extended to other drug carrier systems by using diverse protein-inhibitor pairs that exist in nature.
The cargo release can be triggered by the specific interaction between the protein and its inhibitor. |
doi_str_mv | 10.1039/c6ra03543d |
format | article |
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in vitro
and within cells. This type of bio-switch may be extended to other drug carrier systems by using diverse protein-inhibitor pairs that exist in nature.
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in vitro
and within cells. This type of bio-switch may be extended to other drug carrier systems by using diverse protein-inhibitor pairs that exist in nature.
The cargo release can be triggered by the specific interaction between the protein and its inhibitor.</description><subject>Cargo</subject><subject>Complex formation</subject><subject>Drug delivery systems</subject><subject>Gating systems</subject><subject>Nanoparticles</subject><subject>Proteins</subject><subject>Switches</subject><subject>Vehicles</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpNkEtLAzEURoMoWGo37oUsRRjNa_JYlvrEgiC6HpLMrY1MJzXJIP57Ryvq3dxvcfi49yB0TMk5JdxceJks4bXg7R6aMCJkxYg0-__yIZrl_ErGkTVlkk7Q_Ry3aXjBCTqwGXB-D8WvsRtzi2OPtykWCH0V-nVwocSE87BNdhM78ENnEw59gWR9CbE_Qgcr22WY_ewper6-elrcVsuHm7vFfFl5pmWplNbAWyH0SkJtlLWMKyEU8wSIUtwQzRyl3hEtwbnWgxMjz40Fo0Rb13yKTne943FvA-TSbEL20HW2hzjkhmoyPqxMrUb0bIf6FHNOsGq2KWxs-mgoab6kNQv5OP-WdjnCJzs4Zf_L_Unln9pxaRI</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Wang, Xiaoliang</creator><creator>Liu, Pengchang</creator><creator>Chen, Zhijun</creator><creator>Shen, Jiacong</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20160101</creationdate><title>A drug release switch based on protein-inhibitor supramolecular interaction</title><author>Wang, Xiaoliang ; Liu, Pengchang ; Chen, Zhijun ; Shen, Jiacong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c286t-788e3d448f6e597aa2374472c0e07739082b11cb086ebbdceb4e3d39ae974d553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Cargo</topic><topic>Complex formation</topic><topic>Drug delivery systems</topic><topic>Gating systems</topic><topic>Nanoparticles</topic><topic>Proteins</topic><topic>Switches</topic><topic>Vehicles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Xiaoliang</creatorcontrib><creatorcontrib>Liu, Pengchang</creatorcontrib><creatorcontrib>Chen, Zhijun</creatorcontrib><creatorcontrib>Shen, Jiacong</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Xiaoliang</au><au>Liu, Pengchang</au><au>Chen, Zhijun</au><au>Shen, Jiacong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A drug release switch based on protein-inhibitor supramolecular interaction</atitle><jtitle>RSC advances</jtitle><date>2016-01-01</date><risdate>2016</risdate><volume>6</volume><issue>3</issue><spage>2548</spage><epage>25484</epage><pages>2548-25484</pages><issn>2046-2069</issn><eissn>2046-2069</eissn><abstract>In this report, we describe a new system in which mesoporous silica nanoparticles (MSNs) are gated with α-chymotrypsin A protein (CTRA) and the cargoes within the vehicles are released in the presence of phenylmethanesulfonyl fluoride (PMSF), a canonical inhibitor of CTRA. This cargo release switch is based on the specific interaction between CTRA and PMSF as well as structural changes upon their supramolecular complex formation. This host-guest gating system works smoothly both
in vitro
and within cells. This type of bio-switch may be extended to other drug carrier systems by using diverse protein-inhibitor pairs that exist in nature.
The cargo release can be triggered by the specific interaction between the protein and its inhibitor.</abstract><doi>10.1039/c6ra03543d</doi><tpages>5</tpages></addata></record> |
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source | Royal Society of Chemistry |
subjects | Cargo Complex formation Drug delivery systems Gating systems Nanoparticles Proteins Switches Vehicles |
title | A drug release switch based on protein-inhibitor supramolecular interaction |
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