Self-Assembled Peptide-Carbon Nitride Hydrogel as a Light-Responsive Scaffold Material

被引:66
|
作者
Ko, Jong Wan [1 ]
Choi, Woo Seok [1 ]
Kim, Jinhyun [1 ]
Kuk, Su Keun [1 ]
Lee, Sahng Ha [1 ]
Park, Chan Beum [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Mat Sci & Engn, 291 Daehak Ro, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
ARTIFICIAL PHOTOSYNTHESIS; WATER OXIDATION; VISIBLE-LIGHT; PHOTOCATALYTIC ACTIVITY; REDOX BIOCATALYSIS; CATALYSIS; ENZYME; NANOSTRUCTURES; NANOSHEETS; STABILITY;
D O I
10.1021/acs.biomac.7b00889
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Peptide self-assembly is a facile route to the development of bioorganic hybrid materials that have sophisticated nanostructures toward diverse applications. Here, we report the synthesis of self-assembled peptide (Fmoc-diphenylalanine, Fmoc-FF)/graphitic carbon nitride (g-C3N4) hydrogels for light harvesting and biomimetic photosynthesis through noncovalent interactions between aromatic rings in Fmoc-FF nanofibers and tris-s-triazine in g-C3N4 nanosheets. According to our analysis, the photocurrent density of the Fmoc-FF/g-C3N4 hydrogel was 1.8x higher (0.82 mu A cm(-1)) than that of the pristine g-C3N4. This is attributed to effective exfoliation of g-C3N4 nanosheets in the Fmoc-FF/g-C3N4 network, facilitating photoinduced electron transfers. The Fmoc-FF/g-C3N4 hydrogel reduced NAD(+) to enzymatically active NADH under light illumination at a high rate of 0.130 mol g(-1) h(-1) and drove light-responsive redox biocatalysis. Moreover, the Fmoc-FF/g-C3N4 scaffold could well-encapsulate key photosynthetic components, such as electron mediators, cofactors, and enzymes, without noticeable leakage, while retaining their functions within the hydrogel. The prominent activity of the Fmoc-FF/g-C3N4 hydrogel for biomimetic photosynthesis resulted from the easy transfer of photoexcited electrons from electron donors to NAD(+) via g-C3N4 and electron mediators as well as the hybridization of key photosynthetic components in a confined space of the nanofiber network.
引用
收藏
页码:3551 / 3556
页数:6
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