Thermo- and oxidation-responsive homopolypeptide: synthesis, stimuli-responsive property and antimicrobial activity. Issue 17 (3rd April 2019)
- Record Type:
- Journal Article
- Title:
- Thermo- and oxidation-responsive homopolypeptide: synthesis, stimuli-responsive property and antimicrobial activity. Issue 17 (3rd April 2019)
- Main Title:
- Thermo- and oxidation-responsive homopolypeptide: synthesis, stimuli-responsive property and antimicrobial activity
- Authors:
- Liang, Ce
Wang, Xiaodan
Zhou, Rongtao
Shi, Hengchong
Yan, Shunjie
Ling, Ying
Luan, Shifang
Tang, Haoyu - Abstract:
- Abstract : We present the design and synthesis of a side-chain functional polypeptide with a thioether spacer that is readily decorated to produce thermo- and oxidation-responsive polymers with antimicrobial activity. Abstract : A homopolypeptide with a thioether spacer and a reactive chloro side-chain end group, namely PBLG-S-Cl, can be readily prepared by n -butylamine initiated ring-opening polymerization of γ-4-(substituent)benzyl-l -glutamate acid based N -carboxyanhydride (NCA) monomer. Cationic polypeptides (PBLG-S-ImX, X = I, BF4 ) with upper critical solution temperature (UCST)-type thermo- and oxidation-responsive properties were prepared by nucleophilic substitution of PBLG-S-Cl and subsequent ion-exchange reaction. OEGylated polypeptides (PBLG-S-OEG7 ) with lower critical solution temperature (LCST)-type thermo- and oxidation-responsive properties were prepared by nucleophilic substitution of PBLG-S-Cl with NaN3 yielding PBLG-S-N3, followed by 1, 3-dipolar cycloaddition. CD analysis revealed a thermally stable α-helical conformation of the resulting cationic polypeptides in aqueous solution. The α-helical conformation and long hydrophobic spacer enable PBLG-S-ImX (X = Cl, I, BF4 ) samples with good growth inhibition of S. aureus . The antimicrobial activity of PBLG-S-ImX (X = I, BF4 ) samples was found to be temperature independent. Yet, the antimicrobial activity was affected by the oxidation of thioether bonds as well as the oxidation/degradation ofAbstract : We present the design and synthesis of a side-chain functional polypeptide with a thioether spacer that is readily decorated to produce thermo- and oxidation-responsive polymers with antimicrobial activity. Abstract : A homopolypeptide with a thioether spacer and a reactive chloro side-chain end group, namely PBLG-S-Cl, can be readily prepared by n -butylamine initiated ring-opening polymerization of γ-4-(substituent)benzyl-l -glutamate acid based N -carboxyanhydride (NCA) monomer. Cationic polypeptides (PBLG-S-ImX, X = I, BF4 ) with upper critical solution temperature (UCST)-type thermo- and oxidation-responsive properties were prepared by nucleophilic substitution of PBLG-S-Cl and subsequent ion-exchange reaction. OEGylated polypeptides (PBLG-S-OEG7 ) with lower critical solution temperature (LCST)-type thermo- and oxidation-responsive properties were prepared by nucleophilic substitution of PBLG-S-Cl with NaN3 yielding PBLG-S-N3, followed by 1, 3-dipolar cycloaddition. CD analysis revealed a thermally stable α-helical conformation of the resulting cationic polypeptides in aqueous solution. The α-helical conformation and long hydrophobic spacer enable PBLG-S-ImX (X = Cl, I, BF4 ) samples with good growth inhibition of S. aureus . The antimicrobial activity of PBLG-S-ImX (X = I, BF4 ) samples was found to be temperature independent. Yet, the antimicrobial activity was affected by the oxidation of thioether bonds as well as the oxidation/degradation of counteranions. … (more)
- Is Part Of:
- Polymer chemistry. Volume 10:Issue 17(2019)
- Journal:
- Polymer chemistry
- Issue:
- Volume 10:Issue 17(2019)
- Issue Display:
- Volume 10, Issue 17 (2019)
- Year:
- 2019
- Volume:
- 10
- Issue:
- 17
- Issue Sort Value:
- 2019-0010-0017-0000
- Page Start:
- 2190
- Page End:
- 2202
- Publication Date:
- 2019-04-03
- Subjects:
- Polymers -- Periodicals
Macromolecules -- Periodicals
Polymerization -- Periodicals
547.705 - Journal URLs:
- http://www.rsc.org/Publishing/Journals/PY/Index.asp ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8py01735b ↗
- Languages:
- English
- ISSNs:
- 1759-9954
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.703400
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 10133.xml