Microfluidic droplet detection and sorting

US10710078B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10710078-B2
Application numberUS-201615569201-A
CountryUS
Kind codeB2
Filing dateApr 29, 2016
Priority dateApr 30, 2015
Publication dateJul 14, 2020
Grant dateJul 14, 2020

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention relates to the field of microfluidics and in particular to methods for detecting microfluidic droplets and particles within droplets, as well as sorting the droplets. These methods allow for quantifying properties and activities of the particles within the droplets. For this purpose, the invention provides microfluidic droplets comprising suitably labelled particles. The invention also provides microfluidic devices and systems having properties which make them particularly suitable for use in the methods of the invention.

First claim

Opening claim text (preview).

The invention claimed is: 1. A microfluidic droplet comprising a first particle associated with an amount of a first detectable label, and a potential particle binding partner associated with an amount of a second detectable label, wherein the amount of the first detectable label is known and/or substantially identical to the amount of the first detectable label associated with a further particle comprised in a further microfluidic droplet, wherein the first detectable label is different from the second detectable label, and wherein the further microfluidic droplet is comprised in a plurality of microfluidic droplets also comprising said microfluidic droplet comprising said first particle, and wherein the potential particle binding partner is one of an antibody, antibody derivative, antibody mimetic, a bacteriophage, an mRNA-polypeptide complex, an mRNA-ribosome-polypeptide complex, a cell, a virus, a peptide, a protein, a nucleic acid, an aptamer and a small molecule. 2. The microfluidic droplet of claim 1 , wherein the first particle is associated with the second detectable label via binding to the potential particle binding partner. 3. The microfluidic droplet of claim 1 , wherein the first and further particle are selected from the group consisting of a cell, a virus, a bead, a protein and a nanoparticle. 4. The microfluidic droplet of claim 1 , wherein the microfluidic droplet further comprises, associated with an amount of a third detectable label, (i) a particle non-binder or (ii) a second particle not binding the potential particle binding partner. 5. A method for quantifying the binding between a particle and a potential particle binding partner in a microfluidic droplet according to claim 1 , comprising the steps of (i) measuring the signal of the first detectable label, (ii) measuring the signal of the second detectable label, and (iii) normalizing the signal of the second detectable label using the signal of the first detectable label, wherein the normalized signal of the second detectable label represents the quantity of binding between the particle and the potential particle binding partner. 6. A method for screening potential particle binding partners, comprising the steps of: (a) feeding a microfluidic droplet comprising a potential particle binding partner-producing cell and a reporter cell into a detection channel, the detection channel comprising a detection point, and wherein the reporter cell signals the effect of a potential particle binding partner produced by the potential particle binding partner-producing cell via a second detectable label, and wherein the reporter cell further comprises a first detectable label, and (b) detecting a first detectable label and the second detectable label of the reporter cell, comprised in the microfluidic droplet at the detection point, and (c) normalizing the signal of the second detectable label using the signal of the first detectable label, wherein the potential particle binding partner is one of an antibody, antibody derivative, antibody mimetic, a bacteriophage, an mRNA-polypeptide complex, an mRNA-ribosome-polypeptide complex, a cell, a virus, a peptide, a protein, a nucleic acid, an aptamer and a small molecule. 7. The method according to claim 6 , further comprising constricting at least the vertical movement of said cells within the microfluidic droplet at least at the detection point in the detection channel, compared to the same microfluidic droplet when having a spherical shape. 8. The method according to claim 6 , further comprising step (d) sorting the microfluidic droplet according to the normalized signal. 9. The method according to claim 6 , further comprising a preparation step (a′) before step (a), comprising the encapsulation of the potential particle binding partner-producing cell and reporter cell into the microfluidic droplet and incubating the potential particle binding partner-producing cell and the reporter cell for an amount of time sufficient for secretion of antibodies inside the droplets. 10. A method for quantifying the effect of a potential particle binding partner on a particle in a microfluidic droplet according to claim 1 , comprising the steps of (i) measuring the signal of the first detectable label, (ii) measuring the signal of the second detectable label, and (iii) normalizing the signal of the second detectable label using the signal of the first detectable label, wherein the normalized signal of the second detectable label represents the quantity of effect of the potential particle binding partner on the particle. 11. The method according to claim 10 , wherein the particle is a reporter cell, and wherein the reporter cell signals by the second detectable label the effect of the particle binding partner on the reporter cell.

Assignees

Inventors

Classifications

  • G01N33/58Primary

    involving labelled substances (G01N33/53 takes precedence) · CPC title

  • for blood cell populations (red blood cells G01N33/80) · CPC title

  • microstructural devices · CPC title

  • the analysis being performed on a sample stream · CPC title

  • Sorting or classification of particles or molecules · CPC title

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What does patent US10710078B2 cover?
The present invention relates to the field of microfluidics and in particular to methods for detecting microfluidic droplets and particles within droplets, as well as sorting the droplets. These methods allow for quantifying properties and activities of the particles within the droplets. For this purpose, the invention provides microfluidic droplets comprising suitably labelled particles. The i…
Who is the assignee on this patent?
European Molecular Biology Laboratory
What technology area does this patent fall under?
Primary CPC classification G01N33/58. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Jul 14 2020 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).