Multifunctional Stimuli-Responsive Cellulose Nanocrystals via Dual Surface Modification with Genetically Engineered Elastin-Like Polypeptides and Poly(acrylic acid)

被引:20
|
作者
Malho, Jani-Markus [1 ,5 ]
Brand, Jeremie [1 ]
Pecastaings, Gilles [1 ]
Ruokolainen, Janne [2 ]
Groeschel, Andre [3 ,4 ]
Sebe, Gilles [1 ]
Garanger, Elisabeth [1 ]
Lecommandoux, Sebastien [1 ]
机构
[1] Univ Bordeaux, CNRS, LCPO, Bordeaux INP,UMR5629, F-33607 Pessac, France
[2] Aalto Univ, Sch Sci, Dept Appl Phys, POB 15100, Aalto 00076, Finland
[3] Univ Duisburg Essen, Phys Chem, D-45127 Essen, Germany
[4] Univ Duisburg Essen, Ctr Nanointegrat CENIDE, D-45127 Essen, Germany
[5] Nolla Antimicrobial Oy, Viikinkaari 4, Helsinki 00790, Finland
来源
ACS MACRO LETTERS | 2018年 / 7卷 / 06期
关键词
NANOCOMPOSITES; NANOPARTICLES; PROTEIN; FUNCTIONALIZATION; CHEMISTRY;
D O I
10.1021/acsmacrolett.8b00321
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Cellulose nanocrystals (CNCs) are promising candidates for a myriad of applications; however, successful utilization of CNCs requires balanced and multifunctional properties, which require ever more applied concepts for supramolecular tailoring. We present here a facile and straightforward route to generate dual functional CNCs using poly(acrylic acid) (PAA) and biosynthetic elastin-like polypeptides (ELPs). We utilize thiol-maleimide chemistry and SI-ATRP to harvest the temperature responsiveness of ELPs and pH sensitivity of PAA to confer multifunctionality to CNCs. Cryo-TEM and light microscopy are used to exhibit reversible temperature response, while atomic force microscopy (AFM) provides detailed information on the particle morphology. The approach is tunable and allows variation of the modifying molecules, inspiring supramolecular engineering beyond the currently presented motifs. The surge of genetically engineered peptides adds further possibilities for future exploitation of the potential of cellulose nanomaterials.
引用
收藏
页码:646 / 650
页数:9
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