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Related Concept Videos

Capillary Electrophoresis: Applications01:30

Capillary Electrophoresis: Applications

Capillary electrophoretic separations offer various modes, each with unique applications. These modes include capillary zone electrophoresis, capillary gel electrophoresis, capillary array electrophoresis, capillary isoelectric focusing, capillary isotachophoresis, micellar electrokinetic chromatography, and capillary electrochromatography.
Capillary zone electrophoresis (CZE) separates ionic components based on their electrophoretic mobility. It has been used to separate proteins, amino acids,...
Two-dimensional Gel Electrophoresis01:22

Two-dimensional Gel Electrophoresis

Two-dimensional gel electrophoresis is a high-resolution protein separation method first introduced by O' Farrell and Klose in 1975. This method involves protein separation by two dimensions, mass and charge, making it more accurate than one-dimensional gel electrophoresis.
The first dimension separation uses the isoelectric focusing or IEF technique performed on immobilized pH gradient (IPG) strips that separate proteins according to their isoelectric points.
Biological samples, such as  cells...

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A Nanofilter Array Chip for Fast Gel-Free Biomolecule Separation.

Jianping Fu1, Pan Mao, Jongyoon Han

  • 1Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.

Applied Physics Letters
|October 11, 2008
PubMed
Summary

A novel nanofilter array chip enables rapid size-based separation of SDS-protein complexes and DNA molecules using Ogston sieving. This microfabricated technology offers faster molecular separations with potential for further optimization.

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Area of Science:

  • Biotechnology
  • Nanotechnology
  • Analytical Chemistry

Background:

  • Accurate size-based separation of biomolecules like proteins and DNA is crucial for various applications.
  • Existing separation techniques can be time-consuming or lack the required resolution for small molecules.
  • Microfluidic devices offer potential for miniaturized and efficient molecular separations.

Purpose of the Study:

  • To develop and characterize a microfabricated nanofilter array chip for size-fractionating SDS-protein complexes and small DNA molecules.
  • To demonstrate the efficacy of the Ogston sieving mechanism in nanofilter arrays for rapid molecular separations.
  • To explore the scalability and potential for enhanced performance of the nanofilter chip design.

Main Methods:

  • Fabrication of nanofilter arrays with controlled gap sizes ranging from 40-180 nm.
  • Characterization of the nanofilter arrays to assess their physical dimensions and performance.
  • Experimental validation of size-fractionation capabilities using SDS-protein complexes and small DNA molecules.
  • Application of the Ogston sieving principle for separation.

Main Results:

  • Complete size-fractionation of SDS-protein complexes and small DNA molecules was achieved.
  • Separations were accomplished within minutes over a short distance (5 mm).
  • The nanofilter array chip demonstrated effective separation based on the Ogston sieving mechanism.
  • The fabricated nanofilter arrays exhibited gap sizes between 40-180 nm.

Conclusions:

  • The microfabricated nanofilter array chip is a viable technology for rapid, size-based separation of biomolecules.
  • The Ogston sieving mechanism is effectively utilized in these nanofilter arrays for molecular fractionation.
  • The fabrication strategy allows for increased nanofilter density and smaller gap sizes, promising even faster separations in the future.