Bioactive site-specifically modified proteins for 4D patterning of gel biomaterials
Protein-modified biomaterials can be used to modulate cellular function in three dimensions. However, as the dynamic heterogeneous control over complex cell physiology continues to be sought, strategies that permit a reversible and user-defined tethering of fragile proteins to materials remain in gr...
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Veröffentlicht in: | Nature materials 2019-09, Vol.18 (9), p.1005-1014 |
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description | Protein-modified biomaterials can be used to modulate cellular function in three dimensions. However, as the dynamic heterogeneous control over complex cell physiology continues to be sought, strategies that permit a reversible and user-defined tethering of fragile proteins to materials remain in great need. Here we introduce a modular and robust semisynthetic approach to reversibly pattern cell-laden hydrogels with site-specifically modified proteins. Exploiting a versatile sortase-mediated transpeptidation, we generate a diverse library of homogeneous, singly functionalized proteins with bioorthogonal reactive handles for biomaterial modification. We demonstrate the photoreversible immobilization of fluorescent proteins, enzymes and growth factors to gels with excellent spatiotemporal resolution while retaining native protein bioactivity. Localized epidermal growth factor presentation enables dynamic regulation over proliferation, intracellular mitogen-activated protein kinase signalling and subcellularly resolved receptor endocytosis. Our method broadly permits the modification and patterning of a wide range of proteins, which provides newfound avenues to probe and direct advanced cellular fates in four dimensions.
A modular approach of photoreversible patterning of macromolecules with high spatiotemporal resolution within hydrogels is employed to generate biomaterials with controllable cell activity through site-specific immobilization of proteins. |
doi_str_mv | 10.1038/s41563-019-0367-7 |
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A modular approach of photoreversible patterning of macromolecules with high spatiotemporal resolution within hydrogels is employed to generate biomaterials with controllable cell activity through site-specific immobilization of proteins.</description><subject>631/61/2035</subject><subject>631/61/54</subject><subject>631/92/611</subject><subject>631/92/612</subject><subject>639/638/439</subject><subject>Biocompatible Materials</subject><subject>Biological activity</subject><subject>Biomaterials</subject><subject>Biomedical materials</subject><subject>Cell Differentiation</subject><subject>Chemistry and Materials Science</subject><subject>Condensed Matter Physics</subject><subject>Controllability</subject><subject>Fluorescence</subject><subject>Gels</subject><subject>Growth factors</subject><subject>Hydrogels</subject><subject>Immobilization</subject><subject>Kinases</subject><subject>Macromolecules</subject><subject>Materials Science</subject><subject>Nanotechnology</subject><subject>Optical and Electronic Materials</subject><subject>Patterning</subject><subject>Proteins</subject><subject>Proteins - chemistry</subject><subject>Tethering</subject><subject>Tissue Engineering - methods</subject><issn>1476-1122</issn><issn>1476-4660</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kUuLFTEQhYMozkN_gBsJuHHTmsqzeyPo6Kgw4EJdh9ykcs3Q3WmTvgPz783lXscH6KqK1KkvOTmEPAH2ApjoX1YJSouOwdAxoU1n7pFTkEZ3Umt2_9gDcH5Czmq9ZoyDUvohOREADSDNKfn8JmXn13SDtKYVu7qgTzF5N463dMqh9RjoUvKKaa405kLlW7q4dcUyp3lLc6RbHOkm5cm1s-TG-og8iK3g42M9J18v3325-NBdfXr_8eL1Vec1g7WLEAIG3nMTNSoeZFRacQF9UGCaJ4ZeyV4GFT0IDUaLyMB5vdEixI0I4py8OnCX3WbC4HFeixvtUtLkyq3NLtk_J3P6Zrf5xmrDNB9EAzw_Akr-vsO62ilVj-PoZsy7ajkXnA2yN32TPvtLep13ZW72LB_ASM57A_9VcWMkDErtWXBQ-ZJrLRjvngzM7oO1h2Bt-wS7D9aatvP0d693Gz-TbAJ-ENQ2mrdYfl39b-oPKDGtwA</recordid><startdate>20190901</startdate><enddate>20190901</enddate><creator>Shadish, Jared A.</creator><creator>Benuska, Gabrielle M.</creator><creator>DeForest, Cole A.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>3V.</scope><scope>7SR</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>K9.</scope><scope>KB.</scope><scope>L6V</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7S</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1529-4286</orcidid><orcidid>https://orcid.org/0000-0003-0337-3577</orcidid></search><sort><creationdate>20190901</creationdate><title>Bioactive site-specifically modified proteins for 4D patterning of gel biomaterials</title><author>Shadish, Jared A. ; 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Mater</stitle><addtitle>Nat Mater</addtitle><date>2019-09-01</date><risdate>2019</risdate><volume>18</volume><issue>9</issue><spage>1005</spage><epage>1014</epage><pages>1005-1014</pages><issn>1476-1122</issn><eissn>1476-4660</eissn><abstract>Protein-modified biomaterials can be used to modulate cellular function in three dimensions. However, as the dynamic heterogeneous control over complex cell physiology continues to be sought, strategies that permit a reversible and user-defined tethering of fragile proteins to materials remain in great need. Here we introduce a modular and robust semisynthetic approach to reversibly pattern cell-laden hydrogels with site-specifically modified proteins. Exploiting a versatile sortase-mediated transpeptidation, we generate a diverse library of homogeneous, singly functionalized proteins with bioorthogonal reactive handles for biomaterial modification. We demonstrate the photoreversible immobilization of fluorescent proteins, enzymes and growth factors to gels with excellent spatiotemporal resolution while retaining native protein bioactivity. Localized epidermal growth factor presentation enables dynamic regulation over proliferation, intracellular mitogen-activated protein kinase signalling and subcellularly resolved receptor endocytosis. Our method broadly permits the modification and patterning of a wide range of proteins, which provides newfound avenues to probe and direct advanced cellular fates in four dimensions.
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subjects | 631/61/2035 631/61/54 631/92/611 631/92/612 639/638/439 Biocompatible Materials Biological activity Biomaterials Biomedical materials Cell Differentiation Chemistry and Materials Science Condensed Matter Physics Controllability Fluorescence Gels Growth factors Hydrogels Immobilization Kinases Macromolecules Materials Science Nanotechnology Optical and Electronic Materials Patterning Proteins Proteins - chemistry Tethering Tissue Engineering - methods |
title | Bioactive site-specifically modified proteins for 4D patterning of gel biomaterials |
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