Continuous biomolecule separation in a nanofilter

Abstract

This invention provides a method and an apparatus for quickly continuously fractionating biomolecules, such as DNAs, proteins and carbohydrates by taking advantage of differential bidirectional transport of biomolecules with varying physico-chemical characteristics, for example size, charge, hydrophobicity, or combinations thereof, through periodic arrays of microfabricated nanofilters. The passage of biomolecules through the nanofilter is a function of both steric and electrostatic interactions between charged macromolecules and charged nanofilter walls, Continuous-flow separation through the devices of this invention are applicable for molecules varying in terms of any molecular properties (e.g., size, charge density or hydrophobicity) that can lead to differential transport across the nanofilters.

Description

CROSS REFERENCE TO RELATED APPLICATIONS [0001] This Application claims the benefit of U.S. Provisional Application Ser. No. 60 / 723,926, filed Oct. 6, 2005, which is hereby incorporated in its entirety.GOVERNMENT INTEREST STATEMENT [0002] This invention was made in whole or in part with government support under grant number CTS-0347348, awarded by the National Science Foundation. The government may have certain rights in the invention.FIELD OF THE INVENTION [0003] This invention is directed to sorting devices comprising nanoseparation matrices, an apparatus comprising the same, and methods of use thereof for high throughput molecular separations. BACKGROUND OF THE INVENTION [0004] In systems biology, and in the application of biomarker detection and biosensing, the separation and identification of many proteins, small molecules, and carbohydrates from a cell or from complex biological samples, is necessary. Often, one needs to profile the concentrations of many different biomarkers, ...

AI Technical Summary

Benefits of technology

[0033] In one embodiment, the sorting is charge-based. According to this aspect of the invention and in one

Problems solved by technology

However, these biomarkers (typically smaller than 30 kD) are present at relatively low concentrations (pM˜nM), while majority proteins (albumin and globulins, typically larger than 40 kD) are present at much higher concentrations (μM˜mM), which critically limits the detection of the smaller biomarkers.

Pre-fractionation and separation could eliminate background molecules to enhance the detection ability of the signaling molecules, but none of the conventional separation techniques is appropriate for this task.

Gel electrophoresis is routinely used for separating proteins based on size, but they are generally slow and hard to automate, and require bulky equipment.

Capillary Electrophoresis (CE) with a liquid sieving matrix is currently the fastest size-based separation technique for protein, but polymeric sieving matrix can interfere with downstream separation and detection processes, which limits the automation of the entire sample preparation process.

While microfluidic biomolecule separation systems hold much promise for miniaturizing and automating biomolecule analysis processes, most adopt the same gel sieve material in their separation, with all inherent limitations of the conventional techniques.

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