Green Polymers toward Nanobiotechnology(I): Synthesis of Glycopolypeptides and Their Analogues

doi:10.21127/yaoyigc20190010

General Chemistry ›› 2019, Vol. 5 ›› Issue (3): 190010-190010.DOI: 10.21127/yaoyigc20190010

Special Issue: Nanomaterials

• Perspectives • Previous Articles Next Articles

Green Polymers toward Nanobiotechnology(I): Synthesis of Glycopolypeptides and Their Analogues

Zhao Wang^a, Ana Rute Neves^b, Filipe Olim^b, Helena Tomás^b, Shi Tang^{c, *}, Ruilong Sheng^{b, *}

a Department of Materials, Jinling Institute of Technology, Nanjing, Jiangsu 211169, China;
b CQM-Centro de Química da Madeira, Universidade da Madeira, Campus da Penteada, 9000-390 Funchal, Portugal;
c College of Chemistry and Chemical Engineering, Jishou University, Jishou, Hunan 416000, China

Received:2019-04-04 Online:2019-09-29 Published:2019-09-28
Contact: Ruilong Sheng , Email: ruilong.sheng@staff.uma.pt (R. S.); Tel: +351-291705254

Abstract

Abstract: Harnessing natural-based renewable molecular resources to construct functional synthetic green polymers is a promising research frontier at the interface of sustainable/green chemistry, polymer chemistry and nanobiotechnology. As natural glycoprotein mimics/analogues and biocompatible building blocks of nanobio- materials, synthetic functional glycopolypeptides and their structural/functional analogues have attracted great attentions in recent years. This mini-perspective article reviewed current synthetic strategies and methods of glycopolypeptides and their analogues. The pros and cons of the synthesis protocols were discussed, moreover, possible future perspectives in this field were also stated.

Key words: glycopolypeptide, green polymer, synthesis, perspective

Zhao Wang, Ana Rute Neves, Filipe Olim, Helena Tomás, Shi Tang, Ruilong Sheng. Green Polymers toward Nanobiotechnology(I): Synthesis of Glycopolypeptides and Their Analogues[J]. General Chemistry, 2019, 5(3): 190010-190010.

References

[1] Bonduelle C.; Lecommandoux S. Biomacromolecules2013, 14, 2973.; b) Krannig, K. S.; Schlaad, H.Soft Matter 2014, 10, 4228.
[2] Miura, Y. Polym. J. 2012, 44, 679; (b) Kiessling, L. L.; Grim, J. C. Chem. Soc. Rev. 2013, 42, 4476; (c) Bonduelle, C.; Oliveira, H.; Gauche, C.; Huang, J.; Heise, A.; Lecommandoux, S. Chem. Commun. 2016, 52, 11251.
[3] Xiao C. S.; Ding J. X.; He C. L.; Chen, X. Acta Polym. Sinica2018, 1, 45.
(1)Kramer J. R.; Deming, T. J. Polym. Chem.2014, 5, 671; (b) Deming, T. [J].Chem. Rev., 2016, 116, 786.
[4] Gauche C.; Lecommandoux S. Polymer2016, 107, 474; (b) Rhodes, A. J.; Deming, T. [J].ACS Macro Lett. 2013, 2, 351;(c) Yang, H. K.; Bao, J. F.; Mo, L.; Yang, R. M.; Xu, X. D.; Tang, W. J.; Lin, J. T.; Wang, G. H.; Zhang, L. M.; Jiang, X. Q. RSC Adv. 2017, 7, 21093;, 3981
(e) Kramer J. R.; Deming T. J. Biomacromolecules2012, 13, 1719.
[5] Kramer J. R.; Deming, T. J. Chem. Commun.2013, 49, 5144
(b) Krannig K. S.; Doriti A.; Schlaad H. Macromolecules2014, 47, 2536.
[6] Kramer J. R.; Deming, T. J. J. Am. Chem. Soc.2010, 132, 15068.
(2)Kramer J. R.; Deming, T. J. J. Am. Chem. Soc.2012, 134, 4112
(b) Krannig K. S.; Doriti A.; Schlaad H. Macromolecules2014, 47, 2536.
[7] Bonduelle C.; Mazzaferro S.; Huang J.; Lambert O.; Heise A.; Lecommandoux S. Faraday Discuss.2013, 137; (b) Mohamed Wali, A. R.; Zhou, J.; Ma, S.; He, Y.; Yue, D.; Tang, J. Z.; Gu, Z.Int. J. Pharm. 2017, 525, 191;(c) Pranantyo, D.; Xu, L. Q.; Hou, Z.; Kang, E. T.; Chan-Park, M. B. Polym. Chem. 2017, 8, 3364.
[8] Upadhyay K. K.; Meins, J.-F. Le; Misra, A.; Voisin P.; Bouchaud V.; Ibarboure E.; Schatz C.; Lecommandoux S. Biomacromolecules2009, 10, 2802
(b) Yang H. K.; Zhang, L.-M. M. Mater. Sci. Eng. C. Mater. Biol. Appl.2014, 41, 36.
[9] Fu L.; Sun C.; Yan L.ACS Appl. Mater. Interfaces 2015, 7, 2104
(b) Wang Z.; Sheng R.; Luo T.; Sun J.; Cao A. Polym. Chem.2017, 8, 472.
[10] Wang Z.; Luo T.; Sheng R.; Li H.; Sun J.; Cao A. Biomacromolecules2015, 17, 98; (b) Sun, J.; Sheng, R.; Luo, T.; Wang, Z.; Li, H. Cao, A.J. Mater. Chem. B. 2016, 4, 4696
(c) Wang Z.; Luo T.; Cao A.; Sun J.; Jia L.; Sheng R. Nanomaterials2018, 8, 136.
[11] Zhou M.; Delaveris C.; Kramer J.; Kenkel J.; Engleman. E.; Bertozzi, C. Angew. Chem. Int. Ed. 2018, 57, 3137
(b) Pandey B.; Patil N.; Bhosle G.; Ambade A.; Gupta S. Bioconjugate Chem.2019, 30, 633.
[12] Pati D.; Das S.; Patil N. G.; Parekh N.; Anjum D. H.; Dhaware V.; Ambade A. V.; Sen Gupta S. Biomacromolecules2016, 17, 466; (b) Liu, Y.; Zhang, Y.; Wang, Z.; Wang, J.; Wei, K.; Chen, G.; Jiang, M.J. Am. Chem. Soc. 2016, 138, 12387;(c) Machado, C.; Smith, I.; Savin, D. Macromolecules 2019, 52, 1899.

Green Polymers toward Nanobiotechnology(I): Synthesis of Glycopolypeptides and Their Analogues

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