a.State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China
b.State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620, China
c.Key Laboratory of Specially Functional Polymeric Materials and Related Technology (ECUST) Ministry of Education, Key Laboratory for Ultrafine Materials of Ministry of Education, Research Center for Biomedical Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China
rliu@ecust.edu.cn
收稿:2020-04-29,
修回:2020-6-8,
录用:2020-6-19,
网络首发:2020-07-30,
纸质出版:2020-06-16
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Wu, Y. M.; Zhang, W. W.; Zhou, R. Y.; Chen, Q.; Xie, C. Y.; Xiang, H. X.; Sun, B.; Zhu, M. F.; Liu, R. H. Facile synthesis of high molecular weight polypeptides , via, fast and moisture insensitive polymerization of , α,-amino acid , N,-carboxyanhydrides. Chinese J. Polym. Sci. 2020, 38, 1131–1140
Yue-Ming Wu, Wei-Wei Zhang, Rui-Yi Zhou, et al. Facile Synthesis of High Molecular Weight Polypeptides
Wu, Y. M.; Zhang, W. W.; Zhou, R. Y.; Chen, Q.; Xie, C. Y.; Xiang, H. X.; Sun, B.; Zhu, M. F.; Liu, R. H. Facile synthesis of high molecular weight polypeptides , via, fast and moisture insensitive polymerization of , α,-amino acid , N,-carboxyanhydrides. Chinese J. Polym. Sci. 2020, 38, 1131–1140 DOI: 10.1007/s10118-020-2471-1.
Yue-Ming Wu, Wei-Wei Zhang, Rui-Yi Zhou, et al. Facile Synthesis of High Molecular Weight Polypeptides
Polypeptides have been widely utilized in the fields of biomaterials and biomedicine. Ever since
N
-carboxyanhydride (NCA) was reported by Hermann Leuchs in 1906
ring-opening polymerization of NCAs has been extensively used to prepare polypeptides. Despite continuous innovations
it is still challenging to synthesize polypeptides in high molecular weight efficiently. To address this challenge
we developed KHMDS/NaHMDS initiated fast NCA polymerization that is also moisture tolerant
open-flask amenable and terminal tunable. This NCA polymerization was able to proceed in most common solvents and meet the solubility requirement of variable NCA monomers and corresponding polypeptides. KHMDS can initiate
γ
-benzyl-L-glutamate-
N
-carboxyanhydride (BLG NCA) polymerization in a reaction rate 92 times faster than does hexylamine and 80 times faster than does triethylamine. This NCA polymerization also demonstrated easy and fast synthesis of gram-scale long chain polypeptides in an open flask.
Liu, R.; Chen, X.; Gellman, S. H.; Masters, K. S. . Nylon-3 polymers that enable selective culture of endothelial cells . J. Am. Chem. Soc. , 2013 . 135 16296 - 16299 . DOI: 10.1021/ja408634a http://doi.org/10.1021/ja408634a .
Zhang, K.; Yan, S.; Li, G.; Cui, L.; Yin, J. . In-situ birth of MSCs multicellular spheroids in poly(L-glutamic acid)/chitosan scaffold for hyaline-like cartilage regeneration . Biomaterials , 2015 . 71 24 - 34 . DOI: 10.1016/j.biomaterials.2015.08.037 http://doi.org/10.1016/j.biomaterials.2015.08.037 .
Liu, T.; Zhang, Y. F.; Liu, S. Y. . Drug and plasmid DNA co-delivery nanocarriers based on abctype polypeptide hybrid miktoarm star copolymers . Chinese J. Polym. Sci. , 2013 . 31 924 - 937 . DOI: 10.1007/s10118-013-1281-0 http://doi.org/10.1007/s10118-013-1281-0 .
Liu, H.; Xiao, Y.; Xu, H.; Guan, Y.; Zhang, J.; Lang, M. . Reversible thermo-sensitivity induced from varying the hydrogen bonding between the side residues of rationally designed polypeptides . Chem. Commun. , 2015 . 51 10174 - 10177 . DOI: 10.1039/C5CC03017J http://doi.org/10.1039/C5CC03017J .
Guo, A.; Yang, W.; Yang, F.; Yu, R.; Wu, Y. . Well-defined poly( γ -benzyl-L-glutamate)- g -polytetrahydrofuran: synthesis, characterization, and properties . Macromolecules , 2014 . 47 5450 - 5461 . DOI: 10.1021/ma501060y http://doi.org/10.1021/ma501060y .
Herce, H. D.; Schumacher, D.; Schneider, A. F. L.; Ludwig, A. K.; Mann, F. A.; Fillies, M.; Kasper, M. A.; Reinke, S.; Krause, E.; Leonhardt, H.; Cardoso, M. C.; Hackenberger, C. P. R. . Cell-permeable nanobodies for targeted immunolabelling and antigen manipulation in living cells . Nat. Chem. , 2017 . 9 762 - 771 . DOI: 10.1038/nchem.2811 http://doi.org/10.1038/nchem.2811 .
Lee, M. W.; Han, M.; Bossa, G. V.; Snell, C.; Song, Z.; Tang, H.; Yin, L.; Cheng, J.; May, S.; Luijten, E.; Wong, G. C. . Interactions between membranes and "metaphilic" polypeptide architectures with diverse side-chain populations . ACS Nano , 2017 . 11 2858 - 2871 . DOI: 10.1021/acsnano.6b07981 http://doi.org/10.1021/acsnano.6b07981 .
Hou, Y.; Zhou, Y.; Wang, H.; Wang, R.; Yuan, J.; Hu, Y.; Sheng, K.; Feng, J.; Yang, S.; Lu, H. . Macrocyclization of interferon-poly(alpha-amino acid) conjugates significantly improves the tumor retention, penetration, and antitumor efficacy . J. Am. Chem. Soc. , 2018 . 140 1170 - 1178 . DOI: 10.1021/jacs.7b13017 http://doi.org/10.1021/jacs.7b13017 .
Wu, X.; Wu, Y.; Ye, H.; Yu, S.; He, C.; Chen, X. . Interleukin-15 and cisplatin co-encapsulated thermosensitive polypeptide hydrogels for combined immuno-chemotherapy . J. Control. Release , 2017 . 255 81 - 93 . DOI: 10.1016/j.jconrel.2017.04.011 http://doi.org/10.1016/j.jconrel.2017.04.011 .
He, H.; Zheng, N.; Song, Z. Y.; Kim, K. H.; Yao, C.; Zhang, R. J.; Zhang, C. L.; Huang, Y. H.; Uckun, F. M.; Cheng, J. J.; Zhang, Y. F.; Yin, L. C. . Suppression of hepatic inflammation via systemic siRNA delivery by membrane-disruptive and endosomolytic helical polypeptide hybrid nanoparticles . ACS Nano , 2016 . 10 1859 - 1870 . DOI: 10.1021/acsnano.5b05470 http://doi.org/10.1021/acsnano.5b05470 .
Mowery, B. P.; Lee, S. E.; Kissounko, D. A.; Epand, R. F.; Epand, R. M.; Weisblum, B.; Stahl, S. S.; Gellman, S. H. . Mimicry of antimicrobial host-defense peptides by random copolymers . J. Am. Chem. Soc. , 2007 . 129 15474 - 15476 . DOI: 10.1021/ja077288d http://doi.org/10.1021/ja077288d .
Zhou, C.; Qi, X.; Li, P.; Chen, W. N.; Mouad, L.; Chang, M. W.; Leong, S. S.; Chan-Park, M. B. . High potency and broad-spectrum antimicrobial peptides synthesized via ring-opening polymerization of α -aminoacid- N -carboxyanhydrides . Biomacromolecules , 2010 . 11 60 - 67 . DOI: 10.1021/bm900896h http://doi.org/10.1021/bm900896h .
Tang, H.; Zhang, D. . General route toward side-chain-functionalized α -helical polypeptides . Biomacromolecules , 2010 . 11 1585 - 1592 . DOI: 10.1021/bm1002174 http://doi.org/10.1021/bm1002174 .
Li, P.; Zhou, C.; Rayatpisheh, S.; Ye, K.; Poon, Y. F.; Hammond, P. T.; Duan, H.; Chan-Park, M. B. . Cationic peptidopolysaccharides show excellent broad-spectrum antimicrobial activities and high selectivity . Adv. Mater. , 2012 . 24 4130 - 4137 . DOI: 10.1002/adma.201104186 http://doi.org/10.1002/adma.201104186 .
Ong, Z. Y.; Wiradharma, N.; Yang, Y. Y. . Strategies employed in the design and optimization of synthetic antimicrobial peptide amphiphiles with enhanced therapeutic potentials . Adv. Drug Deliv. Rev. , 2014 . 78 28 - 45 . DOI: 10.1016/j.addr.2014.10.013 http://doi.org/10.1016/j.addr.2014.10.013 .
Wang, M.; Zhou, C.; Chen, J.; Xiao, Y.; Du, J. . Multifunctional biocompatible and biodegradable folic acid conjugated poly( ε -caprolactone)-polypeptide copolymer vesicles with excellent antibacterial activities . Bioconjug. Chem. , 2015 . 26 725 - 734 . DOI: 10.1021/acs.bioconjchem.5b00061 http://doi.org/10.1021/acs.bioconjchem.5b00061 .
Xiong, M.; Han, Z.; Song, Z.; Yu, J.; Ying, H.; Yin, L.; Cheng, J. . Bacteria-assisted activation of antimicrobial polypeptides by a random-coil to helix transition . Angew. Chem. Int. Ed. , 2017 . 56 10826 - 10829 . DOI: 10.1002/anie.201706071 http://doi.org/10.1002/anie.201706071 .
Teng, P.; Ma, N.; Cerrato, D. C.; She, F.; Odom, T.; Wang, X.; Ming, L. J.; van der Vaart, A.; Wojtas, L.; Xu, H.; Cai, J. . Right-handed helical foldamers consisting of de novo D-AApeptides . J. Am. Chem. Soc. , 2017 . 139 7363 - 7369 . DOI: 10.1021/jacs.7b03007 http://doi.org/10.1021/jacs.7b03007 .
Gao, Y. F.; Dong, C. M. . Triple redox/temperature responsive diselenide-containing homopolypeptide micelles and supramolecular hydrogels thereof . J. Polym. Sci., Part A: Polym. Chem. , 2018 . 56 1067 - 1077 . DOI: 10.1002/pola.28984 http://doi.org/10.1002/pola.28984 .
Zhang, S.; Xiao, X. M.; Qi, F.; Ma, P. C.; Zhang, W. W.; Dai, C. Z.; Zhang, D. F.; Liu, R. H. . Biofilm disruption utilizing alpha/beta chimeric polypeptide molecular brushes . Chinese J. Polym. Sci. , 2019 . 37 1105 - 1112 . DOI: 10.1007/s10118-019-2278-0 http://doi.org/10.1007/s10118-019-2278-0 .
Huang, J. G.; Li, J. C.; Lyu, Y.; Miao, Q. Q.; Pu, K. . Molecular optical imaging probes for early diagnosis of drug-induced acute kidney injury . Nat. Mater. , 2019 . 18 1133 - 1143 . DOI: 10.1038/s41563-019-0378-4 http://doi.org/10.1038/s41563-019-0378-4 .
Xu, D. Z.; Liu, M. Y.; Huang, Q.; Chen, J. Y.; Huang, H. Y.; Deng, F. J.; Tian, J. W.; Wen, Y. Q.; Zhang, X. Y.; Wei, Y. . A novel method for the preparation of fluorescent C 60 poly(amino acid) composites and their biological imaging . J. Colloid Interf. Sci. , 2018 . 516 392 - 397 . DOI: 10.1016/j.jcis.2018.01.085 http://doi.org/10.1016/j.jcis.2018.01.085 .
Wu, L.; Zou, Y.; Deng, C.; Cheng, R.; Meng, F.; Zhong, Z. . Intracellular release of doxorubicin from core-crosslinked polypeptide micelles triggered by both pH and reduction conditions . Biomaterials , 2013 . 34 5262 - 5272 . DOI: 10.1016/j.biomaterials.2013.03.035 http://doi.org/10.1016/j.biomaterials.2013.03.035 .
Checco, J. W.; Kreitler, D. F.; Thomas, N. C.; Belair, D. G.; Rettko, N. J.; Murphy, W. L.; Forest, K. T.; Gellman, S. H. . Targeting diverse protein-protein interaction interfaces with α / β -peptides derived from the Z-domain scaffold . Proc. Natl. Acad. Sci. , 2015 . 112 4552 - 4557 . DOI: 10.1073/pnas.1420380112 http://doi.org/10.1073/pnas.1420380112 .
Han, S.; Li, Z.; Zhu, J.; Han, K.; Zeng, Z.; Hong, W.; Li, W.; Jia, H.; Liu, Y.; Zhuo, R.; Zhang, X. . Dual-pH sensitive charge-reversal polypeptide micelles for tumor-triggered targeting uptake and nuclear drug delivery . Small , 2015 . 11 2543 - 2554 . DOI: 10.1002/smll.201402865 http://doi.org/10.1002/smll.201402865 .
Kirberger, S. E.; Maltseva, S. D.; Manulik, J. C.; Einstein, S. A.; Weegman, B. P.; Garwood, M.; Pomerantz, W. C. K. . Synthesis of intrinsically disordered fluorinated peptides for modular design of high-signal (19) F MRI Agents . Angew. Chem. Int. Ed. , 2017 . 56 6440 - 6444 . DOI: 10.1002/anie.201700426 http://doi.org/10.1002/anie.201700426 .
Zhou, X.; Li, Z. . Advances and biomedical applications of polypeptide hydrogels derived from α -amino acid N -carboxyanhydride (NCA) polymerizations . Adv. Healthc. Mater. , 2018 . 7 1800020 DOI: 10.1002/adhm.201800020 http://doi.org/10.1002/adhm.201800020 .
Li, B.; Wu, Y. M.; Zhang, W. J.; Zhang, S.; Shao, N.; Zhang, W. W.; Zhang, L. X.; Fei, J.; Dai, Y. D.; Liu, R. H. . Efficient synthesis of amino acid polymers for protein stabilization . Biomater. Sci. , 2019 . 7 3675 - 3682 . DOI: 10.1039/C9BM00484J http://doi.org/10.1039/C9BM00484J .
Grazon, C.; Salas-Ambrosio, P.; Ibarboure, E.; Buol, A.; Garanger, E.; Grinstaff, M. W.; Lecommandoux, S.; Bonduelle, C. . Aqueous ring-opening polymerization-induced self-assembly (ROPISA) of N-carboxyanhydrides . Angew. Chem. Int. Ed. , 2020 . 59 622 - 626 . DOI: 10.1002/anie.201912028 http://doi.org/10.1002/anie.201912028 .
Duan, Y.; Zheng, H.; Li, Z.; Yao, Y.; Ding, J.; Wang, X.; Nakkala, J. R.; Zhang, D.; Wang, Z.; Zuo, X.; Zheng, X.; Ling, J.; Gao, C. . Unsaturated polyurethane films grafted with enantiomeric polylysine promotes macrophage polarization to a M2 phenotype through PI3K/Akt1/mTOR axis . Biomaterials , 2020 . 246 120012 DOI: 10.1016/j.biomaterials.2020.120012 http://doi.org/10.1016/j.biomaterials.2020.120012 .
Leuchs, H. . Über die Glycin-carbonsaure . Ber. Dtsch. Chem. Ges. , 1906 . 39 857 - 861 . DOI: 10.1002/cber.190603901133 http://doi.org/10.1002/cber.190603901133 .
Lai, H. W.; Chen, X. Y.; Lu, Q.; Bian, Z.; Tao, Y. H.; Wang, X. H. . A new strategy to synthesize bottlebrushes with a helical polyglutamate backbone via N -carboxyanhydride polymerization and RAFT . Chem. Commun. , 2014 . 50 14183 - 14186 . DOI: 10.1039/C4CC06575A http://doi.org/10.1039/C4CC06575A .
Wibowo, S. H.; Sulistio, A.; Wong, E. H.; Blencowe, A.; Qiao, G. G. . Polypeptide films via N -carboxyanhydride ring-opening polymerization (NCA-ROP): past, present and future . Chem. Commun. , 2014 . 50 4971 - 4988 . DOI: 10.1039/c4cc00293h http://doi.org/10.1039/c4cc00293h .
Shen, Y.; Li, Z. B.; Klok, H. A. . Polypeptide brushes grown via surface-initiated ring-opening polymerization of α -amino acid N -carboxyanhydrides . Chinese J. Polym. Sci. , 2015 . 33 931 - 946 . DOI: 10.1007/s10118-015-1654-7 http://doi.org/10.1007/s10118-015-1654-7 .
Song, Z.; Fu, H.; Wang, J.; Hui, J.; Xue, T.; Pacheco, L. A.; Yan, H.; Baumgartner, R.; Wang, Z.; Xia, Y.; Wang, X.; Yin, L.; Chen, C.; Rodriguez-Lopez, J.; Ferguson, A. L.; Lin, Y.; Cheng, J. . Synthesis of polypeptides via bioinspired polymerization of in situ purified N -carboxyanhydrides . Proc. Natl. Acad. Sci. , 2019 . 116 10658 - 10663 . DOI: 10.1073/pnas.1901442116 http://doi.org/10.1073/pnas.1901442116 .
Lv, S.; Kim, H.; Feng, L.; Song, Z.; Yang, Y.; Baumgartner, R.; Tseng, K. Y.; Dillon, S. J.; Leal, C.; Yin, L.; Cheng, J. . Unimolecular polypeptide micelles v i a ultra-fast polymerization of N -carboxyanhydrides . J. Am. Chem. Soc. , 2020 . DOI: 10.1021/jacs.1020c01173 DOI: 10.1021/jacs.1020c01173 http://doi.org/10.1021/jacs.1020c01173 .
Deming, T. J. . Facile synthesis of block copolypeptides of defined architecture . Nature , 1997 . 390 386 - 389 . DOI: 10.1038/37084 http://doi.org/10.1038/37084 .
Deming, T. J. . Transition metal-amine initiators for preparation of well-defined poly( γ -benzyl L-glutamate) . J. Am. Chem. Soc. , 1997 . 119 2759 - 2760 . DOI: 10.1021/ja962625w http://doi.org/10.1021/ja962625w .
Zhao, W.; Lv, Y.; Li, J.; Feng, Z.; Ni, Y.; Hadjichristidis, N. . Fast and selective organocatalytic ring-opening polymerization by fluorinated alcohol without a cocatalyst . Nat. Commun. , 2019 . 10 3590 DOI: 10.1038/s41467-019-11524-y http://doi.org/10.1038/s41467-019-11524-y .
Peng, H.; Ling, J.; Shen, Z. Q. . Ring opening polymerization of α -amino acid N -carboxyanhydrides catalyzed by rare earth catalysts: polymerization characteristics and mechanism . J. Polym. Sci., Part A: Polym. Chem. , 2012 . 50 1076 - 1085 . DOI: 10.1002/pola.25848 http://doi.org/10.1002/pola.25848 .
Peng, H.; Chen, W. L.; Kong, J.; Shen, Z. Q.; Ling, J. . Synthesis of α -hydroxy- ω -aminotelechelic polypeptide from α -amino acid N -carboxyanhydrides catalyzed by alkali-metal borohydrides . Chinese J. Polym. Sci. , 2014 . 32 743 - 750 . DOI: 10.1007/s10118-014-1445-6 http://doi.org/10.1007/s10118-014-1445-6 .
Lu, H.; Cheng, J. . Hexamethyldisilazane-mediated controlled polymerization of α -amino acid N -carboxyanhydrides . J. Am. Chem. Soc. , 2007 . 129 14114 - 14115 . DOI: 10.1021/ja074961q http://doi.org/10.1021/ja074961q .
Lu, H.; Cheng, J. . N -trimethylsilyl amines for controlled ring-opening polymerization of amino acid N -carboxyanhydrides and facile end group functionalization of polypeptides . J. Am. Chem. Soc. , 2008 . 130 12562 - 12563 . DOI: 10.1021/ja803304x http://doi.org/10.1021/ja803304x .
Yuan, J.; Sun, Y.; Wang, J.; Lu, H. . Phenyl trimethylsilyl sulfide-mediated controlled ring-opening polymerization of α -amino acid N -carboxyanhydrides . Biomacromolecules , 2016 . 17 891 - 896 . DOI: 10.1021/acs.biomac.5b01588 http://doi.org/10.1021/acs.biomac.5b01588 .
Dimitrov, I.; Schlaad, H. . Synthesis of nearly monodisperse polystyrene-polypeptide block copolymers via polymerisation of N -carboxyanhydrides . Chem. Commun. , 2003 . 2944 - 2945 . .
Conejos-Sanchez, I.; Duro-Castano, A.; Birke, A.; Barz, M.; Vicent, M. J. . A controlled and versatile NCA polymerization method for the synthesis of polypeptides . J. Polym. Sci., Part A: Polym. Chem. , 2013 . 4 3182 - 3186 . .
Vacogne, C. D.; Schlaad, H. . Primary ammonium/tertiary amine-mediated controlled ring opening polymerisation of amino acid N -carboxyanhydrides . Chem. Commun. , 2015 . 51 15645 - 15648 . DOI: 10.1039/C5CC06905J http://doi.org/10.1039/C5CC06905J .
Bhaw-Luximon, A.; Jhurry, D.; Belleney, J.; Goury, V. . Polymerization of γ -methylglutamate N -carboxyanhydride using Al-Schiff's base complexes as initiators . Macromolecules , 2003 . 36 977 - 982 . DOI: 10.1021/ma0214310 http://doi.org/10.1021/ma0214310 .
Zhang, H. Y.; Nie, Y. Z.; Zhi, X. M.; Du, H. F.; Yang, J. . Controlled ring-opening polymerization of α -amino acid N -carboxy-anhydride by frustrated amine/borane Lewis pairs . Chem. Commun. , 2017 . 53 5155 - 5158 . DOI: 10.1039/C7CC01440F http://doi.org/10.1039/C7CC01440F .
Yuan, J. S.; Zhang, Y.; Li, Z. Z.; Wang, Y. Y.; Lu, H. . A S-Sn Lewis pair-mediated ring-opening polymerization of α -amino acid N -carboxyanhydrides: fast kinetics, high molecular weight, and facile bioconjugation . ACS Macro Lett. , 2018 . 7 892 - 897 . DOI: 10.1021/acsmacrolett.8b00465 http://doi.org/10.1021/acsmacrolett.8b00465 .
Zhao, W.; Gnanou, Y.; Hadjichristidis, N. . Organocatalysis by hydrogen-bonding: a new approach to controlled/living polymerization of α -amino acid N -carboxyanhydrides . J. Polym. Sci., Part A: Polym. Chem. , 2015 . 6 6193 - 6201 . .
Zou, J.; Fan, J.; He, X.; Zhang, S.; Wang, H.; Wooley, K. L. . A facile glovebox-free strategy to significantly accelerate the syntheses of well-defined polypeptides by N -carboxyanhydride (NCA) ring opening polymerizations . Macromolecules , 2013 . 46 4223 - 4226 . DOI: 10.1021/ma4007939 http://doi.org/10.1021/ma4007939 .
Aliferis, T.; Iatrou, H.; Hadjichristidis, N. . Living polypeptides . Biomacromolecules , 2004 . 5 1653 - 1656 . DOI: 10.1021/bm0497217 http://doi.org/10.1021/bm0497217 .
Habraken, G. J. M.; Wilsens, K. H. R. M.; Koning, C. E.; Heise, A. . Optimization of N -carboxyanhydride (NCA) polymerization by variation of reaction temperature and pressure . Polym. Chem. , 2011 . 2 1322 - 1330 . .
Pickel, D. L.; Politakos, N.; Avgeropoulos, A.; Messman, J. M. . A mechanistic study of α -(amino acid)- N -carboxyanhydride polymerization: comparing initiation and termination events in high-vacuum and traditional polymerization techniques . Macromolecules , 2009 . 42 7781 - 7788 . DOI: 10.1021/ma901340y http://doi.org/10.1021/ma901340y .
Vayaboury, W.; Giani, O.; Cottet, H.; Deratani, A.; Schue, F. . Living polymerization of α -amino acid N -carboxyanhydrides (NCA) upon decreasing the reaction temperature . Macromol. Rapid Commun. , 2004 . 25 1221 - 1224 . DOI: 10.1002/marc.200400111 http://doi.org/10.1002/marc.200400111 .
Habraken, G. J. M.; Peeters, M.; Dietz, C. H. J. T.; Koning, C. E.; Heise, A. . How controlled and versatile is N -carboxy anhydride (NCA) polymerization at 0 °C? Effect of temperature on homo-, block- and graft (co)polymerization . J. Polym. Sci., Part A: Polym. Chem. , 2010 . 1 514 - 524 . .
Wu, Y.; Zhang, D.; Ma, P.; Zhou, R.; Hua, L.; Liu, R. . Lithium hexamethyldisilazide initiated superfast ring opening polymerization of α -amino acid N -carboxyanhydrides . Nat. Commun. , 2018 . 9 5297 DOI: 10.1038/s41467-018-07711-y http://doi.org/10.1038/s41467-018-07711-y .
Ding, J. D. . Glovebox free and rapid ring-opening polymerization of α -amino acid N -carboxyanhydrides in open-vessels . J. Funct. Polym , 2019 . 32 120 - 122 . .
Wan, X. H.; Wang, X. H. . Catalytic system for superfast polypeptide synthesis under atmosphere condition . Acta Polymerica Sinica (in Chinese) , 2019 . 50 99 - 101 . .
Luan, S. F . Facile preparation of polypeptides: moisture insensitive and superfast ring opening polymerization of N -carboxyanhydrides . Mater. Rep. , 2019 . 33 1 - 2 . .
Huesmann, D.; Birke, A.; Klinker, K.; Turk, S.; Rader, H. J.; Barz, M. . Revisiting secondary structures in NCA polymerization: influences on the analysis of protected polylysines . Macromolecules , 2014 . 47 928 - 936 . DOI: 10.1021/ma5000392 http://doi.org/10.1021/ma5000392 .
Neufeld, R.; Michel, R.; Herbst-Irmer, R.; Schone, R.; Stalke, D. . Introducing a hydrogen-bond donor into a weakly nucleophilic bronsted base: alkali metal hexamethyldisilazides (MHMDS, M = Li, Na, K, Rb and Cs) with ammonia . Chem. Eur. J. , 2016 . 22 12340 - 12346 . DOI: 10.1002/chem.201600833 http://doi.org/10.1002/chem.201600833 .
Kricheldorf, H. R. . Polypeptides and 100 years of chemistry of α -amino acid N -carboxyanhydrides . Angew. Chem. Int. Ed. , 2006 . 45 5752 - 5784 . DOI: 10.1002/anie.200600693 http://doi.org/10.1002/anie.200600693 .
Kuo, S. W.; Tsai, H. T. . Control of peptide secondary structure on star shape polypeptides tethered to polyhedral oligomeric silsesquioxane nanoparticle through click chemistry . Polymer , 2010 . 51 5695 - 5704 . DOI: 10.1016/j.polymer.2010.10.005 http://doi.org/10.1016/j.polymer.2010.10.005 .
Yu, S. L.; Xiang, X. H.; Zholu, J. L.; Qiu, T.; Hu, Z. X.; Zhu, M. F. . Typical polymer fiber materials: an overview and outlook . Acta Polymerica Sinica (in Chinese) , 2020 . 51 39 - 54 . .
Guo, L.; Lahasky, S. H.; Ghale, K.; Zhang, D. H. . N -heterocyclic carbene-mediated zwitterionic polymerization of N -substituted N -carboxyanhydrides toward poly( α -peptoid)s: kinetic, mechanism, and architectural control . J. Am. Chem. Soc. , 2012 . 134 9163 - 9171 . DOI: 10.1021/ja210842b http://doi.org/10.1021/ja210842b .
Kricheldorf, H. R.; von Lossow, C.; Schwarz, G. . Cyclic polypeptides by solvent-induced polymerizations of α -amino acid N -carboxyanhydrides . Macromolecules , 2005 . 38 5513 - 5518 . DOI: 10.1021/ma0401368 http://doi.org/10.1021/ma0401368 .
Schmid, R. . Re-interpretation of the solvent dielectric constant in coordination chemical terms . J. Sol. Chem. , 1983 . 12 135 - 152 . DOI: 10.1007/BF00645354 http://doi.org/10.1007/BF00645354 .
Deng, C.; Wu, J.; Cheng, R.; Meng, F.; Klok, H.; Zhong, Z. . Functional polypeptide and hybrid materials: precision synthesis via α -amino acid N -carboxyanhydride polymerization and emerging biomedical applications . Prog. Polym. Sci. , 2014 . 39 330 - 364 . DOI: 10.1016/j.progpolymsci.2013.10.008 http://doi.org/10.1016/j.progpolymsci.2013.10.008 .
Zhou, M.; Qian, Y.; Xie, J.; Zhang, W.; Jiang, W.; Xiao, X.; Chen, S.; Dai, C.; Cong, Z.; Ji, Z.; Shao, N.; Liu, L.; Wu, Y.; Liu, R. . Poly(2-oxazoline)-based functional peptide mimics: eradicating MRSA infections and persisters while alleviating antimicrobial resistance . Angew. Chem. Int. Ed. , 2020 . 59 6412 - 6419 . DOI: 10.1002/anie.202000505 http://doi.org/10.1002/anie.202000505 .
Idelson, M.; Blout, E. . High molecular weight poly- α ,L-glutamic acid: preparation and optical rotation changes . J. Am. Chem. Soc. , 1958 . 80 4631 - 4634 . DOI: 10.1021/ja01550a056 http://doi.org/10.1021/ja01550a056 .
Seeney, C. E.; Harwood, H. J. . Carbamate ions as propagating species in N -carboxy anhydride polymerizations . J. Macromol. Sci. A Chem. , 1975 . 9 779 - 795 . DOI: 10.1080/00222337508065894 http://doi.org/10.1080/00222337508065894 .
Kricheldorf, H. R.; von Lossow, C.; Schwarz, G. . Tertiary amine catalyzed polymerizations of α -amino acid N -carboxyanhydrides: the role of cyclization . J. Polym. Sci., Part A: Polym. Chem. , 2006 . 44 4680 - 4695 . DOI: 10.1002/pola.21553 http://doi.org/10.1002/pola.21553 .
Jiang, W. N.; Xiao, X. M.; Wu, Y. M.; Zhang, W. W.; Cong, Z. H.; Liu, J. J.; Chen, S.; Zhang, H. D.; Xie, J. Y.; Deng, S.; Chen, M. Z.; Wang, Y.; Shao, X. Y.; Dai, Y. D.; Sun, Y.; Fei, J.; Liu, R. H. . Peptide polymer displaying potent activity against clinically isolated multidrug resistant Pseudomonas aeruginosa in vitro and in vivo . Biomater. Sci. , 2020 . 8 739 - 745 . DOI: 10.1039/C9BM01726G http://doi.org/10.1039/C9BM01726G .
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