Literature DB >> 33373527

Self-Assembled Multi- and Single-Chain Glyconanoparticles and Their Lectin Recognition.

Yamin Abdouni1, Gijs M Ter Huurne2, Gokhan Yilmaz3,4, Alessandra Monaco1,4, Carlos Redondo-Gómez1, E W Meijer2, Anja R A Palmans2, C Remzi Becer1,4.   

Abstract

In this work, we describe the physicochemical characterization of amphiphilic glycopolymers synthesized via copper(0)-mediated reversible-deactivation radical polymerization (Cu-RDRP). Depending on the chemical composition of the polymer, these glycopolymers are able to form multi-chain or single-chain polymeric nanoparticles. The folding of these polymers is first of all driven by the amphiphilicity of the glycopolymers and furthermore by the supramolecular formation of helical supramolecular stacks of benzene-1,3,5-tricarboxamides (BTAs) stabilized by threefold hydrogen bonding. The obtained polymeric nanoparticles were subsequently evaluated for their lectin-binding affinity toward a series of mannose- and galactose-binding lectins via surface plasmon resonance. We found that addition of 2-ethylhexyl acrylate to the polymer composition results in compact particles, which translates to a reduction in binding affinity, whereas with the addition of BTAs, the relation between the nature of the particle and the binding ability system becomes more unpredictable.

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Year:  2020        PMID: 33373527     DOI: 10.1021/acs.biomac.0c01486

Source DB:  PubMed          Journal:  Biomacromolecules        ISSN: 1525-7797            Impact factor:   6.988


  1 in total

1.  Controlling Amphiphilic Polymer Folding beyond the Primary Structure with Protein-Mimetic Di(Phenylalanine).

Authors:  Jacqueline L Warren; Peter A Dykeman-Bermingham; Abigail S Knight
Journal:  J Am Chem Soc       Date:  2021-08-10       Impact factor: 16.383

  1 in total

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