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[[File:202001 nanopore sequencing.svg|thumb|right|320px|Principle of nanopore sequencing. Source: Wikimedia Commons, CC BY 4.0.]]
[[File:202001 nanopore sequencing.svg|thumb|right|320px|Principle of nanopore sequencing. Source: Wikimedia Commons, CC BY 4.0.]]
'''Nanopore technology''' is part of the Nanopore Wiki learning path. Nanopore technology uses nanometer-scale openings to detect molecules through changes in ionic current, tunneling current, optical signal, or other measurable readouts.
'''Nanopore technology''' is part of the Wiki learning path. Nanopore technology uses nanometer-scale openings to detect molecules through changes in ionic current, tunneling current, optical signal, or other measurable readouts.


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Revision as of 11:42, 30 June 2026

File:202001 nanopore sequencing.svg
Principle of nanopore sequencing. Source: Wikimedia Commons, CC BY 4.0.

Nanopore technology is part of the Wiki learning path. Nanopore technology uses nanometer-scale openings to detect molecules through changes in ionic current, tunneling current, optical signal, or other measurable readouts.

Core concepts

  • The pore geometry defines the sensing volume and constrains which molecules can be resolved.
  • Biological pores offer reproducible atomic structures; solid-state pores offer material and device flexibility.
  • Signal quality depends on pore state, membrane or chip stability, electronics, chemistry, and analysis.
  • Sequencing is one engineered application of a broader nanopore detection principle.

How a measurement is organized

Step Description
1 Choose the pore system and define the target molecule.
2 Prepare buffer, sample, membrane or chip, and low-noise recording conditions.
3 Record an open-pore baseline and verify that the system is stable.
4 Add sample, detect events, and compare with controls and metadata.

Typical applications

  • DNA and RNA sequencing.
  • Protein, peptide, polymer, particle, and small-molecule sensing.
  • Single-channel biophysics and pore engineering.
  • Portable, real-time molecular analysis.

Common pitfalls

  • Assuming all nanopores behave like commercial sequencing flow cells.
  • Ignoring surface adsorption and non-specific interactions.
  • Comparing data across platforms without matching bandwidth, voltage, buffer, and pore size.

References