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A Method for Selecting Structure-switching Aptamers Applied to a Colorimetric Gold Nanoparticle Assay
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Aptamers: Universal capture units for lateral flow applications.

Christin Fischer1, Hauke Wessels1, Angelika Paschke-Kratzin1

  • 1Hamburg School of Food Science; Institute of Food Chemistry, University of Hamburg, Grindelallee 117, 20146 Hamburg, Germany.

Analytical Biochemistry
|January 24, 2017
PubMed
Summary
This summary is machine-generated.

Aptamers successfully function as capture molecules in lateral flow assays for diverse targets, including metabolites, proteins, and spores. This demonstrates their potential as a versatile alternative to antibodies in diagnostic applications.

Keywords:
AptamersCapture moleculesLateral flowLysozymeMetaboliteSmall moleculesSpores

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Area of Science:

  • Biotechnology
  • Analytical Chemistry
  • Biosensors

Background:

  • Antibodies are traditionally used as capture molecules in lateral flow assays.
  • The need for antibody alternatives is driven by ethical considerations and the desire for versatile detection platforms.
  • Aptamers offer a promising alternative due to their stability, specificity, and ease of synthesis.

Purpose of the Study:

  • To demonstrate the efficacy of aptamers as capture molecules in lateral flow assays across various target classes.
  • To establish a universal lateral flow test platform utilizing aptamers.
  • To evaluate aptamers as a viable alternative to antibodies in line with animal protection directives.

Main Methods:

  • Selection and implementation of aptamers for target molecules representing different size classes: p-aminohippuric acid (metabolite), lysozyme (protein), and Alicyclobacillus spores (whole cell).
  • Development of lateral flow assay (LFA) platforms incorporating these aptamers as capture agents.
  • Determination of the limit of detection (LOD) for each target analyte using the aptamer-based LFAs.

Main Results:

  • Successful implementation of aptamers as capture molecules in LFAs, irrespective of target size.
  • Demonstrated detection limits: p-aminohippuric acid in urine (200 ppm), lysozyme in white wine (20 ppm), and Alicyclobacillus spores in orange juice (>8 CFU/mL).
  • Proof-of-concept validation for aptamers in a universal LFA platform.

Conclusions:

  • Aptamers are effective capture molecules for a broad range of targets in lateral flow assay applications.
  • Aptamer-based LFAs provide a versatile and potentially more ethical alternative to traditional antibody-based assays.
  • This study supports the broader adoption of aptamers in diagnostic and analytical testing platforms.