4.6 Article

Glycan heterogeneity on gold nanoparticles increases lectin discrimination capacity in label-free multiplexed bioassays

期刊

ANALYST
卷 141, 期 14, 页码 4305-4312

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6an00549g

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资金

  1. Innovative Uses for Advanced Materials in the Modern World (AM2)
  2. Advantage West Midlands (AWM)
  3. European Regional Development Fund (ERDF)
  4. MOAC doctoral training centre (EPSRC) [EP/F500378/1]
  5. Warwick Institute for Advanced Study
  6. BBSRC Systems Biology doctoral training centre [BB/G530233/1]
  7. ERC [CRYOMAT 638661]
  8. Biotechnology and Biological Sciences Research Council [1090811] Funding Source: researchfish

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The development of new analytical tools as point-of-care biosensors is crucial to combat the spread of infectious diseases, especially in the context of drug-resistant organisms, or to detect biological warfare agents. Glycan/lectin interactions drive a wide range of recognition and signal transduction processes within nature and are often the first site of adhesion/recognition during infection making them appealing targets for biosensors. Glycosylated gold nanoparticles have been developed that change colour from red to blue upon interaction with carbohydrate-binding proteins and may find use as biosensors, but are limited by the inherent promiscuity of some of these interactions. Here we mimic the natural heterogeneity of cell-surface glycans by displaying mixed monolayers of glycans on the surface of gold nanoparticles. These are then used in a multiplexed, label-free bioassay to create 'barcodes' which describe the lectin based on its binding profile. The increased information content encoded by using complex mixtures of a few sugars, rather than increased numbers of different sugars makes this approach both scalable and accessible. These nanoparticles show increased lectin identification power at a range of lectin concentrations, relative to single-channel sensors. It was also found that some information about the concentration of the lectins can be extracted, all from just a simple colour change, taking this technology closer to being a realistic biosensor.

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