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Photosensitive peptide hydrogels as smart materials for applications |
Dongdong Wua, Xian Xiea, Adnan A. Kadib, Yan Zhanga |
a State Key Laboratory of Analytical Chemistry for Life Sciences, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China;
b Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh, Kingdom of Saudi Arabia |
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Guide Photosensitive supramolecular peptide hydrogels with the gelators forming by the integration of photosensitive moieties and peptides have been briefly summarized the hydrogelation capabilities, the expressing manner serving as smart materials, and practical applications. |
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Abstract Photosensitive peptide hydrogels (PPHs) which allow photo-modulation on the self-assembly of peptides were broadly developed over the recent decades. The real-time and spatial modulation of hydrogel properties upon non-contact light illumination, allow the PPHs serving as super "smart" soft materials. Herein, we briefly summarized the PPHs preparing from the integration of diverse photosensitive moieties with peptides through gelation abilities, "smart" manner and applications. Moreover, a novel type of PPHs based on intramolecular biorthogonal photo-click reaction developed by our group has been demonstrated with relative mechanism and applications.
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Received: 21 March 2018
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Fund:We would like to acknowledge the financial support from the National Natural Science Foundation of China (Nos. 21572102, 21672103, 21302093). |
Corresponding Authors:
Yan Zhang, njuzy@nju.edu.cn
E-mail: njuzy@nju.edu.cn
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[1] |
W.C. Chan, P.D. White, Fmoc Solid Phase Peptide Synthesis:A Practical Approach, Oxford University Press, New York, 2000.
|
[2] |
Y. Zhao, H. Yokoi, M. Tanaka, T. Kinoshita, T. Tan, Biomacromolecules 9(2008) 1511-1518.
|
[3] |
Z. Yang, G. Liang, B. Xu, Acc. Chem. Res. 41(2008) 315-326.
|
[4] |
Y. Zhang, H. Gu, Z. Yang, B. Xu, J. Am. Chem. Soc. 125(2003) 13680-13681.
|
[5] |
X. Li, J. Li, Y. Gao, et al., J. Am. Chem. Soc. 132(2010) 17707-17709.
|
[6] |
H. Shigemitsu, T. Fujisaku, S. Onogi, et al., Nat. Protoc. 11(2016) 1744-1756.
|
[7] |
M. Zhou, A.M. Smith, A.K. Das, et al., Biomaterials 30(2009) 2523-2530.
|
[8] |
V. Jayawarna, S.M. Richardson, A.R. Hirst, et al., Acta Biomater. 5(2009) 934-943.
|
[9] |
H. Geng, Q. Zong, J. You, et al., Sci. China Chem. 59(2016) 1-10.
|
[10] |
Z. Yang, G. Liang, M. Ma, Y. Gao, B. Xu, J. Mater. Chem. 17(2007) 850-854.
|
[11] |
Y. Kuang, B. Xu, Angew. Chem. 52(2013) 6944-6948.
|
[12] |
C. Ou, J. Zhang, X. Zhang, Z. Yang, M. Chen, Chem. Commun. 49(2013) 1853-1855.
|
[13] |
H. Cui, M.J. Webber, S.I. Stupp, Biopolymers 94(2010) 1-18.
|
[14] |
M.P. Hendricks, K. Sato, L.C. Palmer, S.I. Stupp, Acc. Chem. Res. 50(2017) 2440-2448.
|
[15] |
S.W. Liao, T.B. Yu, Z. Guan, J. Am. Chem. Soc. 131(2009) 17638-17646.
|
[16] |
K. Chawla, T.B. Yu, S.W. Liao, Z. Guan, Biomacromolecules 12(2011) 560-567.
|
[17] |
X. Li, Y. Kuang, J. Shi, et al., J. Am. Chem. Soc. 133(2011) 17513-17518.
|
[18] |
D. Wu, J. Zhou, J. Shi, X. Du, B. Xu, Chem. Commun. 50(2014) 1992-1994.
|
[19] |
A.G. Cheetham, R.W. Chakroun, W. Ma, H. Cui, Chem. Soc. Rev. 46(2017) 6638-6663.
|
[20] |
J. Li, Y. Kuang, Y. Gao, et al., J. Am. Chem. Soc. 135(2013) 542-545.
|
[21] |
Y. Zhou, X. Li, Chin. Chem. Lett. 28(2017) 1835-1840.
|
[22] |
X. Du, J. Zhou, J. Shi, B. Xu, Chem. Rev. 115(2015) 13165-13307.
|
[23] |
J. Wang, J. Zheng, Y. Cai, et al., Sci. China Chem. 59(2016) 719-723.
|
[24] |
W. Wang, J. Hu, M. Zheng, et al., Org. Biomol. Chem. 13(2015) 11492-11498.
|
[25] |
Z. Qiu, H. Yu, J. Li, Y. Wang, Y. Zhang, Chem. Commun. 23(2009) 3342-3344.
|
[26] |
Y. Huang, Z. Qiu, Y. Xu, et al., Org. Biomol. Chem. 9(2011) 2149-2155.
|
[27] |
X. Li, Y. Gao, Y. Kuang, B. Xu, Chem. Commun. 46(2010) 5364-5366.
|
[28] |
W. Li, I.S. Park, S.K. Kang, M. Lee, Chem. Commun. 48(2012) 8796-8798.
|
[29] |
Y. Lin, Y. Qiao, P. Tang, Z. Li, J. Huang, Soft Matter 7(2011) 2762-2769.
|
[30] |
M. Ikeda, T. Tanida, T. Yoshii, I. Hamachi, Adv. Mater. 23(2011) 2819-2822.
|
[31] |
C.D.G. Lux, J. Lux, G. Collet, et al., Biomacromolecules 16(2015) 3286-3296.
|
[32] |
T. Yoshii, M. Ikeda, I. Hamachi, Angew. Chem. 53(2014) 7264-7267.
|
[33] |
T.M. Doran, D.M. Ryan, B.L. Nilsson, Polym. Chem. 5(2013) 241-248.
|
[34] |
J.K. Sahoo, S.K. Nalluri, N. Javid, H. Webb, R.V. Ulijn, Chem. Commun. 50(2014) 5462-5464.
|
[35] |
W. Xiong, H. Zhou, C. Zhang, H. Lu, Chin. Chem. Lett. 28(2017) 2125-2128.
|
[36] |
L.A. Haines, K. Rajagopal, B. Ozbas, et al., J. Am. Chem. Soc. 127(2005) 17025-17029.
|
[37] |
T. Muraoka, C.Y. Koh, H. Cui, S.I. Stupp, Angew. Chem. 121(2009) 6060-6063.
|
[38] |
R.V. Rughani, M.C. Branco, D.J. Pochan, J.P. Schneider, Macromolecules 43(2010) 7924-7930.
|
[39] |
Y. Ding, Y. Li, M. Qin, Y. Cao, W. Wang, Langmuir 29(2013) 13299-13306.
|
[40] |
S.H. Kim, Y. Sun, J.A. Kaplan, M.W. Grinstaff, J.R. Parquette, New J. Chem. 39(2015) 3225-3228.
|
[41] |
C.W. Chu, B.J. Ravoo, Chem. Commun. 53(2017) 12450-12453.
|
[42] |
H. Komatsu, S. Tsukiji, M. Ikeda, I. Hamachi, J. Chem-Asian 6(2011) 2368-2375.
|
[43] |
D.J. Smith, G.A. Brat, S.H. Medina, et al., Nat. Nanotechnol. 11(2016) 95-102.
|
[44] |
M. He, J. Li, S. Tan, R. Wang, Y. Zhang, J. Am. Chem. Soc.135(2013) 18718-18721.
|
[45] |
J. Li, R. Kooger, M. He, et al., Chem. Commun. 50(2014) 3722-3724.
|
[46] |
Z. Zhou, Q. Yi, T. Xia, et al., Org. Biomol. Chem. 15(2017) 2191-2198.
|
[47] |
Z. Zhou, X. Xie, Q. Yi, et al., Org. Biomol. Chem. 15(2017) 6892-6895.
|
[48] |
J. Kim, I.S. Kim, T.H. Cho, et al., Biomaterials 28(2007) 1830-1837.
|
[49] |
A. Sanchez-Ferrero, A. Mata, M.A. Mateos-Timoneda, et al., Biomaterials 68(2015) 42-53.
|
[50] |
A.T. Neffe, B.F. Pierce, G. Tronci, et al., Adv. Mater. (Weinheim Ger.) 27(2015) 1738-1744.
|
[51] |
S. Zhang, Y. Guo, Y. Dong, et al., Acs Appl. Mater. Inter. 8(2016) 13242-13250.
|
[52] |
B. Gupta, R. Agarwal, M.S. Alam, Biomed. Hydrogels (2011) 184-227.
|
[53] |
T. Ito, C. Yoshida, Y. Murakami, Mater. Sci. Eng. C 33(2013) 3697-3703.
|
[54] |
D.H. Phuc, N.T. Hiep, D.N.P. Chau, et al., Int. J. Polym. Sci. 2016(2016) 6723716.
|
[55] |
A. Kumar, S.S. Han, Int. J. Polym. Mater. Polym. Biomater. 66(2017) 159-182.
|
[56] |
S.Ahadian, R.B. Sadeghian, S. Salehi, et al., BioconjugateChem. 26(2015) 1984-2001.
|
[57] |
A. Motealleh, N.S. Kehr, Adv. Healthc. Mater. 6(2017) 1600938.
|
[58] |
M. Mehrali, A. Thakur, C.P. Pennisi, et al., Adv. Mater. 29(2017) 1603612.
|
[59] |
P.M. Kharkar, K.L. Kiick, A.M. Kloxin, Chem. Soc. Rev. 42(2013) 7335-7372.
|
[60] |
G. Huang, F. Li, X. Zhao, et al., Chem. Rev. 117(2017) 12764-12850.
|
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|
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