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Quantifying the interactions of bacteria with external ligands is fundamental to the understanding of pathogenesis, antibiotic resistance, immune evasion, and mechanism of antimicrobial action. Due to inherent cell-to-cell heterogeneity in

Quantifying the interactions of bacteria with external ligands is fundamental to the understanding of pathogenesis, antibiotic resistance, immune evasion, and mechanism of antimicrobial action. Due to inherent cell-to-cell heterogeneity in a microbial population, each bacterium interacts differently with its environment. This large variability is washed out in bulk assays, and there is a need of techniques that can quantify interactions of bacteria with ligands at the single bacterium level.

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Date Created
  • 2015-01-15
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  • Text
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    Identifier
    • Digital object identifier: 10.1016/j.bios.2014.06.069
    • Identifier Type
      International standard serial number
      Identifier Value
      0093-934X
    • Identifier Type
      International standard serial number
      Identifier Value
      1090-2155
    Note
    • NOTICE: this is the author's version of a work that was accepted for publication in BIOSENSORS & BIOELECTRONICS. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in BIOSENSORS & BIOELECTRONICS, 63, 131-137. DOI: 10.1016/j.bios.2014.06.069, opens in a new window

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    This is a suggested citation. Consult the appropriate style guide for specific citation guidelines.

    Syal, Karan, Wang, Wei, Shan, Xiaonan, Wang, Shaopeng, Chen, Hong-Yuan, & Tao, Nongjian (2015). Plasmonic imaging of protein interactions with single bacterial cells. BIOSENSORS & BIOELECTRONICS, 63, 131-137. http://dx.doi.org/10.1016/j.bios.2014.06.069

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