Pickering stabilized peptide gel particles as tunable microenvironments for biocatalysis

We demonstrate the preparation of peptide gel microparticles that are emulsified and stabilized by SiO2 nanoparticles. The gels are composed of aromatic peptide amphiphiles 9-fluorenylmethoxycarbonyldiphenylalanine (Fmoc-FF) coassembled with Fmoc-amino acids with different functional groups (S: seri...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 29(2013), 46 vom: 19. Nov., Seite 14321-7
1. Verfasser: Scott, Gary (VerfasserIn)
Weitere Verfasser: Roy, Sangita, Abul-Haija, Yousef M, Fleming, Scott, Bai, Shuo, Ulijn, Rein V
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't 9-fluorenylmethoxycarbonyl Caprylates Enzymes, Immobilized Fluorenes Fungal Proteins Gels Heptanes Octanols mehr... Peptides Silicon Dioxide 7631-86-9 Lipase EC 3.1.1.3 lipase B, Candida antarctica octanoic acid OBL58JN025
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245 1 0 |a Pickering stabilized peptide gel particles as tunable microenvironments for biocatalysis 
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520 |a We demonstrate the preparation of peptide gel microparticles that are emulsified and stabilized by SiO2 nanoparticles. The gels are composed of aromatic peptide amphiphiles 9-fluorenylmethoxycarbonyldiphenylalanine (Fmoc-FF) coassembled with Fmoc-amino acids with different functional groups (S: serine; D: aspartic acid; K: lysine; and Y: tyrosine). The gel phase provides a highly hydrated matrix, and peptide self-assembly endows the matrix with tunable chemical environments which may be exploited to support and stabilize proteins. The use of Pickering emulsion to stabilize these gel particles is advantageous through avoidance of surfactants that may denature proteins. The performance of enzyme lipase B immobilized in pickering/gel microparticles with different chemical functionalities is investigated by studying transesterification in heptane. We show that the use of Pickering particles enhances the performance of the enzyme, which is further improved in gel-phase systems, with hydrophilic environment provided by Fmoc-FF/S giving rise to the best catalytic performance. The combination of a tunable chemical environment in gel phase and Pickering stabilization described here is expected to prove useful for areas where proteins are to be exploited in technological contexts such as biocatalysis and also in other areas where protein performance and activity are important, such as biosensors and bioinspired solar fuel devices 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Caprylates  |2 NLM 
650 7 |a Enzymes, Immobilized  |2 NLM 
650 7 |a Fluorenes  |2 NLM 
650 7 |a Fungal Proteins  |2 NLM 
650 7 |a Gels  |2 NLM 
650 7 |a Heptanes  |2 NLM 
650 7 |a Octanols  |2 NLM 
650 7 |a Peptides  |2 NLM 
650 7 |a Silicon Dioxide  |2 NLM 
650 7 |a 7631-86-9  |2 NLM 
650 7 |a Lipase  |2 NLM 
650 7 |a EC 3.1.1.3  |2 NLM 
650 7 |a lipase B, Candida antarctica  |2 NLM 
650 7 |a EC 3.1.1.3  |2 NLM 
650 7 |a octanoic acid  |2 NLM 
650 7 |a OBL58JN025  |2 NLM 
700 1 |a Roy, Sangita  |e verfasserin  |4 aut 
700 1 |a Abul-Haija, Yousef M  |e verfasserin  |4 aut 
700 1 |a Fleming, Scott  |e verfasserin  |4 aut 
700 1 |a Bai, Shuo  |e verfasserin  |4 aut 
700 1 |a Ulijn, Rein V  |e verfasserin  |4 aut 
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