4.8 Article

Single-molecule detection of protein efflux from microorganisms using fluorescent single-walled carbon nanotube sensor arrays

Journal

NATURE NANOTECHNOLOGY
Volume 12, Issue 4, Pages 368-377

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/NNANO.2016.284

Keywords

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Funding

  1. Burroughs Wellcome Fund at the Scientific Interface (CASI)
  2. Simons Foundation
  3. BBRF
  4. Beckman Foundation
  5. National Science Foundation (NSF)
  6. Japan Society for the Promotion of Science
  7. Naito Foundation
  8. NSF GRFP fellowship
  9. LAM research fellowship
  10. Hertz Foundation
  11. Department of Defense
  12. NIH Medical Scientist Training Program [T32GM007753]
  13. National Institutes of Health [DP2 OD008435, P50 GM098792]
  14. Office of Naval Research [N00014-13-1-0424]
  15. NSF [MCB-1350625]
  16. Direct For Biological Sciences
  17. Div Of Molecular and Cellular Bioscience [1350625] Funding Source: National Science Foundation
  18. Grants-in-Aid for Scientific Research [15K21770] Funding Source: KAKEN

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A distinct advantage of nanosensor arrays is their ability to achieve ultralow detection limits in solution by proximity placement to an analyte. Here, we demonstrate label-free detection of individual proteins from Escherichia coli (bacteria) and Pichia pastoris (yeast) immobilized in a microfluidic chamber, measuring protein efflux from single organisms in real time. The array is fabricated using non-covalent conjugation of an aptamer-anchor polynucleotide sequence to near-infrared emissive single-walled carbon nanotubes, using a variable chemical spacer shown to optimize sensor response. Unlabelled RAP1 GTPase and HIV integrase proteins were selectively detected from various cell lines, via large near-infrared fluorescent turn-on responses. We show that the process of E. coli induction, protein synthesis and protein export is highly stochastic, yielding variability in protein secretion, with E. coli cells undergoing division under starved conditions producing 66% fewer secreted protein products than their non-dividing counterparts. We further demonstrate the detection of a unique protein product resulting from T7 bacteriophage infection of E. coli, illustrating that nanosensor arrays can enable real-time, single-cell analysis of a broad range of protein products from various cell types.

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