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DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
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Optical Trapping of Nanoparticles
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Single Upconversion Nanoparticle-Bacterium Cotrapping for Single-Bacterium Labeling and Analysis.

Hongbao Xin1,2,3, Yuchao Li4, Dekang Xu4

  • 1Guangdong Provincial Key Laboratory of Optical Fiber Sensing and Communications, Institute of Nanophotonics, Jinan University, Guangzhou, 511443, China.

Small (Weinheim an Der Bergstrasse, Germany)
|January 17, 2017
PubMed
Summary
This summary is machine-generated.

This study introduces a novel optical method for precisely labeling and analyzing individual pathogenic bacteria using upconversion nanoparticles (UCNPs). This technique enables real-time, single-bacterium detection and analysis, crucial for understanding cellular heterogeneity.

Keywords:
optical connectingoptical cotrappingsingle-bacterium analysissingle-bacterium labeling

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Area of Science:

  • Biophotonics
  • Nanotechnology
  • Microbiology

Background:

  • Accurate detection and analysis of pathogenic bacteria are vital for diagnosing infections and guiding antibiotic treatment.
  • Analyzing bacteria at the single-cell level is challenging yet essential for understanding cellular heterogeneity and environmental responses.

Purpose of the Study:

  • To develop an optical strategy for precise single-bacterium labeling and analysis.
  • To demonstrate the cotrapping of single upconversion nanoparticles (UCNPs) with individual bacteria.

Main Methods:

  • Optical trapping of a single upconversion nanoparticle (UCNP) with an average size of ≈120 nm.
  • Simultaneous optical trapping and labeling of both ends of a single bacterium with single UCNPs emitting green light.
  • Real-time detection of signals from bacteria of varying sizes for individual analysis.

Main Results:

  • Successful cotrapping and labeling of individual bacteria with single UCNPs.
  • Demonstrated flexible manipulation of labeled bacteria for targeted analysis.
  • Real-time detection and analysis of signals from individual bacteria were achieved.

Conclusions:

  • The cotrapping method offers a new approach for labeling, detecting, and analyzing single pathogenic bacteria.
  • This technique allows for real-time, single-particle, and single-bacterium level analysis.
  • Enables detailed study of bacterial heterogeneity and responses.