Multiplexed surface enhanced Raman sensors for early disease detection and in-situ bacterial monitoring

Patent metadata

Field	Value
Publication number	US-9987609-B2
Application number	US-201514621306-A
Country	US
Kind code	B2
Filing date	Feb 12, 2015
Priority date	Sep 5, 2014
Publication date	Jun 5, 2018
Grant date	Jun 5, 2018

Abstract

Methods and systems for nanopillar sensors are described. Nanopillars can be defined on a substrate, and metal deposited on the nanopillars. A thermal treatment can reflow the metal on the nanopillars forming metallic bulbs on the top end of the nanopillars. These structures can have enhanced optical detection when functionalized with biological agents, or can detect gases, particles and liquids through interaction with the metal layer on the nanopillars.

First claim

What is claimed is:

1. A method to produce a sensor for multiplexed detection of multiple biomolecules, comprising:
providing a substrate, the substrate comprising at least one recessed region and nanopillars defined in the at least one recessed region;
attaching to said substrate a first plurality of first linkers, each first linker comprising an amine group;
providing a second plurality of second linkers, each second linker capable of binding to a first linker and comprising a photo-uncageable group;
allowing the first and second pluralities of linkers to interact under such conditions and for such a time as to allow binding of some or all of the linkers of the second plurality to some or all of the linkers of the first plurality to generate a third plurality of first and second linkers, each first linker of the third plurality bound to a second linker of the third plurality, and a fourth plurality of first linkers, each first linker of the fourth plurality unbound to a second linker of the fourth plurality;
passivating the linkers of the fourth plurality with a suitable agent; and
performing at least one functionalization step to produce a sensor for multiplexed detection of multiple biomolecules, each functionalization step comprising the steps of:
illuminating at least one area of the substrate to release the second linkers of the third plurality of linkers from being bound to the first linkers of the third plurality of linkers to expose the first linkers of the third plurality attached to the substrate in that area;
providing a plurality of molecular probes capable of attaching to the exposed first linkers of the third plurality;
allowing the molecular probes to interact with the exposed first linkers of the third plurality under such conditions and for such a time as to allow binding of some or all of the molecular probes to some or all of the first linkers of the third plurality to generate a fifth plurality of first linkers, each linker of the fifth plurality bound to a molecular probe, and a sixth plurality of first linkers, each linker of the sixths plurality unbound to a molecular probe; and
passivating the first linkers of the sixth plurality with a suitable agent.

2. The method of claim 1 , wherein at least one first linker of the plurality of first linkers is a thiol-alkane-amine (TAA) linker.

3. The method of claim 1 , wherein at least one second linker of the plurality of second linkers is 7-N,N-diethylamino 4-hydroxymethyl coumarin caged glutamic acid (DECM-CG).

4. The method of claim 1 , wherein the passivating is performed with acetic anhydride.

5. The method of claim 1 , wherein the substrate further comprises metallic bulbs on a top end of the nanopillars.

6. The method of claim 1 , wherein the substrate is silicon.

7. The method of claim 5 , wherein the substrate is silicon, the nanopillars are silicon dioxide and the metallic bulbs are gold, copper, aluminum, platinum, nickel, or silver.

8. The method of claim 1 , wherein the illumination is performed with light at wavelengths between about 350-410 nm.

9. The method of claim 1 , wherein at least one molecular probe of the plurality of molecular probes is an antibody.

10. The method of claim 1 , wherein at least one molecular probe of the plurality of molecular probes is an aptamer.

11. The method of claim 1 , wherein at least one molecular probe of the plurality of molecular probes is a cDNA.

Assignees

• California Inst Of Techn

Inventors

• Walavalkar Sameer
• Scherer Axel

Classifications

• C12Q2600/158

  Expression markers · CPC title

• B01J19/0046 Primary

  Sequential or parallel reactions, e.g. for the synthesis of polypeptides or polynucleotides; Apparatus and devices for combinatorial chemistry or for making molecular arrays (synthesis methods per se C40B50/00) · CPC title

• B01J2219/00585

  Parallel processes · CPC title

• C12Q1/689

  for bacteria · CPC title

• G01N21/65

  Raman scattering · CPC title