Methods and apparatus for monitoring interactions between particles and molecules using nanophotonic trapping

US10241233B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10241233-B2
Application numberUS-201514824423-A
CountryUS
Kind codeB2
Filing dateAug 12, 2015
Priority dateAug 12, 2014
Publication dateMar 26, 2019
Grant dateMar 26, 2019

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Abstract

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A method for characterizing an interaction between a first particle and a second particle is provided. The method includes the steps of: (i) providing an optical trap system including a photonics-based trap, a light source, and a camera; (ii) optically trapping, using the photonics-based trap, the first particle; (iii) obtaining a first measurement of a trap stiffness of the photonics-based trap; (iv) introducing the second particle to the optically trapped particle; (v) incubating the first and second particles under conditions suitable for an interaction between the first and second particles; (vi) obtaining a second measurement of the trap stiffness of the photonics-based trap after the incubation; and (vii) determining, using the first measurement of trap stiffness and the second measurement of trap stiffness, a property of the interaction between the first particle and the second particle.

First claim

Opening claim text (preview).

What is claimed is: 1. A label-free method for characterizing an interaction between a first unlabeled biomolecular particle and a second unlabeled biomolecular particle, the method comprising the steps of: providing an optical trap system, the optical trap system comprising a photonic crystal resonator having a light source directed thereto for exciting the photonic crystal resonator and a camera positioned above a trapping site in the photonic crystal resonator; radiating light from the light source in proximity of the trapping site in the photonic crystal resonator; optically trapping the first unlabeled biomolecular particle with a first known refractive index in the photonic crystal resonator using light with a specific minimum power from the light source to induce trapping; wherein the first unlabeled biomolecular particle has a known radius, R 0 ; obtaining a first measurement of Brownian motion while the first unlabeled biomolecular particle is in the photonic crystal resonator based on light scattering captured by the camera from the first unlabeled biomolecular particle; introducing the second unlabeled biomolecular particle with a second known refractive index into the photonic crystal resonator; incubating the first and second unlabeled biomolecular particle under conditions suitable for binding said first and second unlabeled biomolecular particle to form a complex, wherein the second unlabeled biomolecular particle has a potential affinity for the first unlabeled biomolecular particle; wherein the the first unlabeled particle has a second radius, R′ and R′−R 0 =ΔR; optically trapping the first unlabeled biomolecular particle in the photonic crystal resonator using light with the specific minimum power from the light source to induce trapping after incubation; wherein the first unlabeled biomolecular particle is a virus and the second unlabeled biomolecular particle is an antibody; obtaining a second measurement of Brownian motion of the first unlabeled particle in the photonic crystal resonator after incubation based on light scattering captured by the camera from the first unlabeled biomolecular particle; obtaining a relative Brownian motion measurement, defined as a comparison of the first and second measurements of Brownian motion, of the first unlabeled particle after incubation and based on light scattered by the first unlabeled particle captured by the camera; analyzing a relationship between the relative Brownian motion measurement of the first unlabeled particle after incubation and ΔR; and determining, using the relationship of the relative Brownian motion measurement of the first unlabeled particle with respect to ΔR, a Brownian motion measurement of the photonic crystal resonator; wherein said relationship provides indication whether a complex is formed.

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Classifications

  • for confining neutral particles or handling confined neutral particles, e.g. atom traps · CPC title

  • with steric inhibition or signal modification, e.g. fluorescent quenching · CPC title

  • Scattering, i.e. diffuse reflection (G01N21/25, G01N21/41 take precedence {G01N21/55 takes precedence}) · CPC title

  • Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands · CPC title

  • Micromanipulators structurally combined with microscopes · CPC title

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What does patent US10241233B2 cover?
A method for characterizing an interaction between a first particle and a second particle is provided. The method includes the steps of: (i) providing an optical trap system including a photonics-based trap, a light source, and a camera; (ii) optically trapping, using the photonics-based trap, the first particle; (iii) obtaining a first measurement of a trap stiffness of the photonics-based tra…
Who is the assignee on this patent?
Univ Cornell
What technology area does this patent fall under?
Primary CPC classification G02B1/005. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Mar 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).