TY - JOUR
T1 - Bioinspired Suprahelical Frameworks as Scaffolds for Artificial Photosynthesis
AU - Tao, Kai
AU - Xue, Bin
AU - Han, Shuyi
AU - Aizen, Ruth
AU - Shimon, Linda J.W.
AU - Xu, Zhengyu
AU - Cao, Yi
AU - Mei, Deqing
AU - Wang, Wei
AU - Gazit, Ehud
N1 - Funding Information: This work was supported in part by the European Research Council under the European Union Horizon 2020 research and innovation program (no. 694426) (E.G.), Joint NSFC-ISF Grant (no. 3145/19) (E.G.), National Natural Science Foundation of China (no.11804148) (B.X.), Natural Science Foundation of Jiangsu province (no. BK20180320) (B.X.), and the Fundamental Research Funds for the Central Universities (no. 020414380118) (B.X.). The authors thank Dr. Ruth Pachter and Dr. Jie Jiang for the band gap calculation assistance, Dr. Sigal Rencus-Lazar for language editing, and the members of Gazit and Cao laboratories for helpful discussions.
PY - 2020/10/7
Y1 - 2020/10/7
N2 - Framework materials have shown promising potential in various biological applications. However, the state-of-the-art components show low biocompatibility or mechanical instability, or cannot integrate both optics and electronics, thus severely limiting their extensive applications in biological systems. Herein, we demonstrate that amide-based bioorganic building blocks, including dipeptides and dipeptide nucleic acids, can self-assemble into hydrogen-bonded suprahelix architectures of controllable handedness, which then form suprahelical frameworks with diverse cavities. Especially, the cavities can be tuned to be hydrophilic or hydrophobic, and the shortest diagonal distance can be modulated from 0.5 to 1.8 nm, with the volume proportion in the unit cell changing from 5 to 60%. Furthermore, the hydrogen bonding networks result in high mechanical rigidity and semiconductively optoelectronic properties, which allow the utilization of the suprahelical frameworks as supramolecular scaffolds for artificial photosynthesis. Our findings reveal amide-based suprahelix architectures acting as bioinspired supramolecular frameworks, thus extending the constituents portfolio and increasing the feasibility of using framework materials for biological applications.
AB - Framework materials have shown promising potential in various biological applications. However, the state-of-the-art components show low biocompatibility or mechanical instability, or cannot integrate both optics and electronics, thus severely limiting their extensive applications in biological systems. Herein, we demonstrate that amide-based bioorganic building blocks, including dipeptides and dipeptide nucleic acids, can self-assemble into hydrogen-bonded suprahelix architectures of controllable handedness, which then form suprahelical frameworks with diverse cavities. Especially, the cavities can be tuned to be hydrophilic or hydrophobic, and the shortest diagonal distance can be modulated from 0.5 to 1.8 nm, with the volume proportion in the unit cell changing from 5 to 60%. Furthermore, the hydrogen bonding networks result in high mechanical rigidity and semiconductively optoelectronic properties, which allow the utilization of the suprahelical frameworks as supramolecular scaffolds for artificial photosynthesis. Our findings reveal amide-based suprahelix architectures acting as bioinspired supramolecular frameworks, thus extending the constituents portfolio and increasing the feasibility of using framework materials for biological applications.
KW - amide-skeleton biomaterials
KW - artificial photosynthesis
KW - crystallization engineering
KW - suprahelices
KW - supramolecular frameworks
UR - http://www.scopus.com/inward/record.url?scp=85092749670&partnerID=8YFLogxK
U2 - 10.1021/acsami.0c13295
DO - 10.1021/acsami.0c13295
M3 - مقالة
C2 - 32924412
SN - 1944-8244
VL - 12
SP - 45192
EP - 45201
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 40
ER -