Methods and systems for detecting biomolecular binding using terahertz radiation

Abstract

Provided herein are methods and systems for detecting biomolecular binding events using gigahertz or terahertz radiation. The methods and systems use low-energy spectroscopy to detect biomolecular binding events between molecules in an aqueous solution. The detected biomolecular binding events include, for example, nucleic acid hybridizations, antibody / antigen binding, and receptor / ligand binding.

Description

CROSS REFERENCE TO RELATED APPLICATION(S) [0001] This application is a divisional application of U.S. application Ser. No. 10 / 911,441 filed Aug. 4, 2004, now pending. The disclosure of the prior application is considered part of and is incorporated by reference in the disclosure of this application.BACKGROUND OF THE INVENTION FIELD OF THE INVENTION [0002] The invention relates generally to detecting a biomolecular binding event and more particularly to detecting such events using spectroscopy. BACKGROUND INFORMATION [0003] Many current methods for detecting disease or the risk of developing a disease rely on detection of one or more biomolecular interactions between a target molecule in the biological sample and a detectable probe molecule. The probe molecule is typically detectable because it is bound to a detectable label. For example, infection in a subject caused by an infectious agent, such as a virus, can be detected by detecting binding of a labeled antibody probe to a viral ...

AI Technical Summary

Benefits of technology

The patent text describes a system and method for detecting biomolecular interactions using terahertz radiation. This technology can be used to detect the presence of infectious agents or genetic mutations in a sample. The method does not require labeling of the molecules, which reduces cost and complexity. However, the current methods for detecting nucleic acid sequences using labeled probes have certain disadvantages, such as increased complexity and background signals. The patent text proposes a system and method that can directly detect the hybridization of nucleic acid molecules without the need for labeling, and can also determine the sequence of the nucleic acid molecule. This technology can be used in various applications, such as detecting disease or monitoring genetic mutations.

Problems solved by technology

However, the inclusion of labels in an assay often makes it more expensive and complicated, and increases the background signal of the assay.

However, these methods are relatively slow and expensive.

As discussed above, this increases the cost and complexity of the method and increases background values, thereby decreasing sensitivity.

Furthermore, inclusion and detection of labels lowers the throughput of the assay.

Although this type of spectroscopy has successfully detected events for smaller molecules (e.g., CO2), it failed to provide the desired level of efficiency and accuracy for biomolecules, which tend to be larger.

Furthermore, the UV / visible / near-infrared radiation causes the molecules to fluoresce, creating background noise that interferes with spectrum signals.

Further, the method requires multiple gratings of strong dispersion to resolve the small frequency change, making the optical instrument too bulky for convenient use.

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