4.7 Article

Efficient Assembly of Quantum Dots with Homogenous Glycans Derived from Natural N-Linked Glycoproteins

Journal

BIOCONJUGATE CHEMISTRY
Volume 29, Issue 9, Pages 3144-3153

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.bioconjchem.8b00477

Keywords

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Funding

  1. National Institutes of Health [R01 NS087070]
  2. National Science Foundation (NSF-CHE) [1058957, 1508501]
  3. Fundacion Ramon Areces
  4. Asahi-Kasei Corp.
  5. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS087070] Funding Source: NIH RePORTER
  6. Division Of Chemistry [1508501] Funding Source: National Science Foundation

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Coating inorganic nanoparticles with polyethylene glycol (PEG)-appended ligands, as means to preserve their physical characteristics and promote steric interactions with biological systems, including enhanced aqueous solubility and reduced immunogenicity, has been explored by several groups. Conversely, macromolecules present in the human serum and on the surface of cells are densely coated with hydrophilic glycans that act to reduce nonspecific interactions, while facilitating specific binding and interactions. In particular, N-linked glycans are abundant on the surface of most serum proteins and are composed of a branched architecture that is typically characterized by a significant level of molecular heterogeneity. Here we provide two distinct methodologies, covalent bioconjugation and self-assembly, to functionalize two types of Quantum Dots with a homogeneous, complex-type N-linked glycan terminated with a sialic acid moiety. A detailed physical and functional characterization of these glycan-coated nanoparticles has been performed. Our findings support the potential use of such fluorescent platforms to sense glycan-involved biological processes, such as lectin recognition and sialidase-mediated hydrolysis.

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