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Issue 12, 2017
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Thermo and pH dual responsive polypeptides derived from “clickable” poly(γ-3-methylthiopropyl-L-glutamate)

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Abstract

Poly(γ-3-methylthiopropyl-L-glutamate) (PMTPLG) with “clickable” thioether groups can be readily prepared from n-butylamine initiated ring-opening polymerization of γ-3-methylthiopropyl-L-glutamic acid based N-carboxyanhydride (MTPLG-NCA). Polypeptides bearing sulfonium moieties and different alkyl (i.e., methyl, n-butyl, and propargyl) pendants were prepared via the alkylation of PMTPLG. They are able to show upper critical solution temperature (UCST)-type thermoresponsive properties in methanol or ethanol depending on the alkyl pendants and counter-anions. Polypeptides bearing sulfonium linkages, ammonium pendants and tetrafluoroborate (BF4) counter-anions (PPLG-MSEA-BF4) were prepared via the copper-mediated [2 + 3] alkyne–azide 1,3-dipolar cycloaddition of polypeptides bearing sulfonium moieties and propargyl pendants, and subsequently ion-exchange reaction. They showed UCST-type thermo and pH dual responsiveness in aqueous solutions. The sharp solution phase separation of PPLG-MSEA-BF4 occurred in a very small pH range (ΔpH = 0.05) when the pH increased from 7.37 to 7.42 as suggested by dynamic light scattering (DLS). The UCST-type phase transition temperature (Tpt) of PPLG-MSEA-BF4 increased by 20 °C as the pH increased from 7.42 to 7.50 as revealed by variable-temperature UV-vis spectroscopy. Increasing polymer or NaBF4 concentrations or decreasing NaCl concentration can further increase the Tpt.

Graphical abstract: Thermo and pH dual responsive polypeptides derived from “clickable” poly(γ-3-methylthiopropyl-l-glutamate)

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Publication details

The article was received on 28 Jan 2017, accepted on 27 Feb 2017 and first published on 28 Feb 2017


Article type: Paper
DOI: 10.1039/C7PY00170C
Citation: Polym. Chem., 2017,8, 1895-1905
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    Thermo and pH dual responsive polypeptides derived from “clickable” poly(γ-3-methylthiopropyl-L-glutamate)

    C. Ge, L. Zhao, Y. Ling and H. Tang, Polym. Chem., 2017, 8, 1895
    DOI: 10.1039/C7PY00170C

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