Integrated microarray printing and detection system for molecular binding analysis

Patent metadata

Field	Value
Publication number	US-10823728-B2
Application number	US-201615204738-A
Country	US
Kind code	B2
Filing date	Jul 7, 2016
Priority date	Jul 8, 2015
Publication date	Nov 3, 2020
Grant date	Nov 3, 2020

Abstract

A method and system for analysis of protein interaction kinetics in microarray or whole-cell based formats includes positioning a sensor chip on a prism. The sensor chip is spotted with a plurality of target molecules. A movable printer head deposits a plurality of analyte droplets on predefined regions of the sensor chip surface. A light source transmits light through the prism to excite surface plasmon resonance on the sensor chip surface, whereby the plurality of target molecules bound to the upper surface are changing the SPR resonance angle and therefore the intensity of the reflected beam. A detector receives reflected light transmitted through the prism from the bottom surface. Signals from the detector are received and processed into kinetic data and microarray labeled data to determine molecular interactions and binding kinetic properties for the plurality of analyte droplets.

First claim

What is claimed is:

1. An integrated microarray printing and detection system (IMPDS) for high-throughput analysis of protein interaction kinetics in microarray or whole-cell based formats comprising:
a prism;
a sensor chip, placed on the prism, the sensor chip having an upper surface and a bottom surface;
a gold plasmon resonance surface on the upper surface of the sensor chip;
a light source configured to illuminate the sensor chip through the prism whereby the sensor chip is activated by the light source;
a lens located to focus reflected light from the bottom surface of the sensor chip;
a camera located to receive the reflected light, where the camera is configured to produce microarray imaging data from the reflected light;
an inkjet printing head located over the sensor chip;
a processor connected to and programmed to control the camera and the inkjet printing head;
where the processor is further programmed to control the inkjet printing head to deposit a plurality of target molecule droplets on a plurality of predetermined regions on the sensor chip in a first phase and then individually deposit a plurality of analyte droplets on the plurality of target molecule droplets in a second phase ,wherein the plurality of target molecule droplets and the plurality of analyte droplets each have a radius of less than 500 μm; and
wherein the processor is further programmed to provide quantitative data also generate quantitative kinetic information from the microarray imagine data produced by the camera.

2. The system of claim 1 wherein the gold plasmon resonance surface of the sensor chip is pre-modified with attachment chemistry comprising activated streptavidin or thiol carboxylic PEG.

3. The system of claim 1 wherein the light source is positioned to illuminate the sensor chip at the surface plasmon resonance angle.

4. The system of claim 1 wherein the processor is further programmed to generate sensorgrams plotting image intensity vs. time profiles that provide quantitative kinetic information of an analyte binding to bacterial cells which may be introduced as droplets by the printing head.

Assignees

• Tao Nongjian
• Wang Shaopeng
• Univ Arizona State

Inventors

• Tao Nongjian
• Wang Shaopeng

Classifications

• G01N2201/122

  Kinetic analysis; determining reaction rate · CPC title

• G01N33/543

  with an insoluble carrier for immobilising immunochemicals · CPC title

• G01N33/557 Primary

  using kinetic measurement, i.e. time rate of progress of an antigen-antibody interaction · CPC title

• G01N21/553

  and using surface plasmons (fluorescence excitation G01N21/648; enhanced Raman G01N21/658) · CPC title