Affinity capture mass spectroscopy with a porous silicon biosensor

• US 20100227414A1
• Filed: 03/05/2010
• Published: 09/09/2010
• Est. Priority Date: 03/05/2009
• Status: Abandoned Application

• Current Assignee: Silicon Kinetics, Inc.
• Original Assignee: Trex Enterprises Corporation
• Inventors: Ervin, John Lawrence
• Application Number:
  US12/660,877
• Publication Number:
  US 20100227414A1
• Time in Patent Office: Days
• US Class Current: 436/501
• CPC Class Codes: G01N 33/6848 Methods of protein analysis involving mass spectrometry

Abstract

Affinity Capture-Mass Spectroscopy (AC-MS), an analytical technique which couples the sensitivity of a label-free binding detected biosensor, and the information richness of mass spectroscopy is described. A 3-dimensional porous silicon bio-surface is used to capture proteins, DNA, or small molecules while acquiring a label-free, time resolved signal linearly proportional to the amount of binding. A switch to dissociative buffer conditions then frees the captured molecule for analysis by mass spectroscopy. In particular, techniques for use with electrospray mass spectroscopy are described.

Claims

1. A process for making label-free molecular ligand-analyte binding measurements comprising the steps of:

A) providing a label-free porous silicon based optical sensor comprising;

a) a spectrometer based optical system comprising at least one light source and two spectrometers,

b) at least one porous silicon region comprising at least 1000 pores, each pore having a nominal width and a nominal depth at least 10 times larger than said nominal width with the depth of at least most of the pores in said porous silicon region defining a top surface and a bottom surface being parallel or approximately parallel to the top surface, said porous silicon region being adapted to permit molecular binding interactions,

c) a computer processor adapted to produce optical path difference information based on output from each of said two spectrometers,

B) providing a mass spectrometer,

C) depositing in a plurality of said at least 1000 pores a fluid containing a ligand chosen to attach to walls of said plurality of said at least 1000 pores,

D) depositing in a said plurality of said at least 1000 pores a fluid containing a buffer and an analyte containing fluid,

E) utilizing the label-free porous silicon based optical sensor to monitor the molecular binding interactions of said ligands and analytes in said analyte containing fluid deposited in said plurality of said at least 1000 pores,

F) separating at least a portion of said buffer from at least a portion of said analytes and analyze with said mass spectrometer said analytes so separated at least one time increment,

G) using information from said optical sensor and said mass spectrometer to characterize molecular binding and disassociation reactions between said analytes and said ligands.

2. The process as in claim 1 wherein said analyte containing fluid contains a plurality of different analyte and information obtained from said mass spectroscope is utilized to identify specific analytes involved in the binding and disassociation reactions.

3. The process as in claim 1 wherein said label-free porous silicon based optical sensor comprises:

A) a single porous silicon flow cell unit,

B) a multiple porous silicon flow cell unit,

C) a micro-well plate adapted to hold a porous silicon chip in a plurality of micro wells,

D) one or more exchangeable format trays adapted to position said single porous silicon flow cell unit, said multiple porous silicon cell unit and said micro-well plate serially within said base unit,

E) a plurality of fluid systems adapted to provide fluids containing buffer solutions, ligand containing solutions, and analyte containing solutions to said single flow cell, said multiple flow cell unit and said micro-well plate, and F) a control system comprising a computer processor adapted to provide automatic optical analysis serially of molecular interactions within the porous silicon chips in said single flow cell, said multiple flow cell or said micro-well plate, depending on which of the three formats is being.

4. The process as in claim 1 wherein said label-free porous silicon based optical sensor is adapted for utilization of porous silicon chips positioned in micro-well plates.

5. The process as in claim 1 wherein said label-free porous silicon based optical sensor is adapted for utilization of porous silicon chips positioned in flow cells.

6. The process as in claim 1 wherein said label-free porous silicon based optical sensor is adapted for utilization of porous silicon chips positioned in flow cells and includes a fraction collector to which output of the flow cells are directed during at least a portion of a period of disassociation phase.

7. The process as in claim 6 wherein the flow to the fraction collector is limited to a desired period soon after the disassociation phase begins so as to collect a sample containing whatever it was that bound to the ligand.

8. The process as in claim 7 wherein the collected sample is analyzed in an electrospray mass spectroscope.

9. The process as in claim 5 wherein a portion or all of output flow from the flow cells is directed to the mass spectroscope for analysis as a function of time.

10. The process as in claim 9 wherein the mass spectroscope in an electrospray spectrometer and a chemical chosen to aid in the electrospray ionization is added to the output flow directed to the mass spectroscope.

11. The process as in claim 5 wherein the label-free porous silicon based optical sensor is equipped with a trap chromatography column adapted to trap portions of fluid flowing from the flow cells.

12. The process as in claim 11 wherein molecules trapped in the trap chromatography are subsequently analyzed with the mass spectroscope permitting simultaneous analysis of many small molecules or peptides.

13. The process as in claim 6 wherein fraction collection is performed at fixed times after disassociation begins.

14. The process as in claim 5 wherein the output of the flow cells are sent to a MALDI spotter for analysis.

15. The process as in claim 4 wherein a well strip comprising posts adapted for the mounting thereon of porous silicon biochips is used to sequentially submerge the biochips into micro-wells in the micro-well plate containing buffer fluid, fluid containing ligands and fluid containing analytes to produce the binding and disassociation reactions.

16. The process as in claim 15 wherein an optical path difference measurement is not performed.