IP Library Granted Patent US 11,561,223
Granted Patent B2
US 11,561,223 · App. 16/641,906 · Granted Jan 24, 2023

Method and system for identifying membrane proteins on extracellular vesicles

Inventors: Jan Lotvall (Boston, MA); Su Chul Jang (Boston, MA); Aleksander Cvjetkovic (Gothenburg, SE); Cecilia Lasser (Gothenburg, SE)
Assignee: Exocure Biosciences Inc.
G01N33/57415G01N33/6848G16B40/10G01N2333/912G01N2560/00G01N2800/7028
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,561,223
App. No.
16/641,906
Granted
Jan 24, 2023
Kind
B2
Abstract

Disclosed is a method of isolating extracellular vesicles and identifying membrane proteins therefrom. The method includes providing human plasma and/or serum; separating lipoproteins and extracellular vesicles from the human plasma and/or serum by a density gradient preparation, collecting the extracellular vesicles from the separated lipoproteins and extracellular vesicles; isolating and purifying the collected extracellular vesicles by using size exclusion chromatography; treating the isolated and purified extracellular vesicles with an aqueous solution to obtain membranes of the extracellular vesicles, wherein the aqueous solution has a pH in a range of 9 to 14; adding salt in a concentration range between 0.5-2.0M to the aqueous solution; isolating the membranes from the treated extracellular vesicles and identifying proteins on the isolated membranes by employing mass spectrometry.

Claims (33)

1. A method of identifying tumor tissue specific-membrane proteins, the method comprising steps of:

(a) isolating extracellular vesicles from a tumor tissue of patients, the isolating comprising:

(i) fragmenting the tissue;

(ii) incubating the fragmented tissue with one or more enzymes to release the extracellular vesicles, wherein the one or more enzymes are selected from a group of proteases including a matrix metalloproteinase, collagenases, and papain and nucleases including DNase, RNase, and Benzonase; and

(iii) separating tissue debris and the extracellular vesicles;

(b) identifying membrane proteins associated with the isolated extracellular vesicles by mass spectrometry;

(c) comparing membrane proteins identified in step (b) with membrane proteins identified as associated with extracellular vesicles isolated from plasma and/or serum sample of healthy subjects by specifically subtracting the membrane proteins identified as associated with extracellular vesicles isolated from plasma and/or serum sample of healthy subjects, to identify tumor tissue-specific membrane proteins; and

(d) creating membrane proteins profiles for the identified tumor tissue-specific membrane proteins.

2. The method of claim 1 , wherein the membrane proteins are identified as associated with extracellular vesicles isolated from plasma and/or serum sample of healthy subjects by a method comprising:

(i) providing human plasma and/or serum;

(ii) separating lipoproteins and extracellular vesicles from the human plasma and/or serum by a density gradient preparation;

(iii) collecting the extracellular vesicles from the separated lipoproteins and extracellular vesicles;

(iv) isolating and purifying the collected extracellular vesicles by using size exclusion chromatography;

(v) treating the isolated and purified extracellular vesicles with an aqueous solution to obtain membranes of the extracellular vesicles, wherein the aqueous solution has a pH in a range of 9 to 14;

(vi) adding salt in a concentration range between 0.5-2.0M to the aqueous solution;

(vii) isolating the membranes from the treated extracellular vesicles; and

(viii) identifying proteins on the isolated membranes by employing mass spectrometry.

3. The method of claim 2 , further comprising (ix) ultracentrifugation of the human plasma and/or serum to concentrate extracellular vesicles therein, wherein the step (ix) is performed before the step (ii).

4. The method of claim 1 , further comprising plotting the created membrane proteins profiles of the patient against pre-determined membrane proteins profiles of healthy tissues and cancerous tissues.

5. The method of claim 4 , wherein the plotting comprises employing at least one of a nanoFCM analysis, ELISA, alphaLISA, FACS, fluorescent correlation microscopy and immune-electron microscopy.

6. The method of claim 1 , wherein the tumor tissue is breast cancer tissue.

7. The method of claim 6 , further comprising plotting the created membrane proteins profiles of the patient against pre-determined membrane proteins profiles of healthy and cancerous breast tissue.

8. The method of claim 7 , wherein breast cancer-specific membrane protein is Receptor tyrosine-protein kinase erbB-2 and/or Cytoskeleton-associated protein 4.

9. A computer program product comprising non-transitory computer-readable storage medium having computer-readable instructions stored thereon, the computer-readable instructions being executable by a computerized device comprising processing hardware to execute a method of identifying tumor tissue specific-membrane proteins, the method comprising steps of:

(a) isolating extracellular vesicles from a tumor tissue of patients, the isolating comprising:

(i) fragmenting the tissue;

(ii) incubating the fragmented tissue with one or more enzymes to release the extracellular vesicles, wherein the one or more enzymes are selected from a group of proteases including a matrix metalloproteinase, collagenases, and papain and nucleases including DNase, RNase, and Benzonase; and

(iii) separating tissue debris and the extracellular vesicles;

(b) identifying membrane proteins associated with the isolated extracellular vesicles by mass spectrometry;

(c) comparing membrane proteins identified in step (b) with membrane proteins identified as associated with extracellular vesicles isolated from plasma and/or serum sample of healthy subjects by specifically subtracting the membrane proteins identified as associated with extracellular vesicles isolated from plasma and/or serum sample of healthy subjects, to identify tumor tissue-specific membrane proteins; and

(d) creating membrane proteins profiles for the identified tumor tissue-specific membrane proteins.

10. The method of claim 7 , wherein the plotting comprises employing at least one of a nanoFCM analysis, ELISA, alphaLISA, FACS, fluorescent correlation microscopy and immune-electron microscopy.

11. The method of claim 1 , wherein separating tissue debris and the extracellular vesicles comprises centrifugation.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE CORRECT THE NATURE OF CONVEYANCE ON THE COVERSHEET FOR THE ORIGINAL RECORDATION, NATURE OF CONVEYANCE SHOULD BE "ASSIGNMENT" AND NOT "CHANGE OF NAME". PREVIOUSLY RECORDED AT REEL: 64189 FRAME: 174. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Nov 12, 2024
From: EXOCURE BIOSCIENCES, INC.
To: EXOCURE SWEDEN AB
Reel/Frame 069530/0601 →
CHANGE OF NAME Recorded Jul 7, 2023
From: EXOCURE BIOSCIENCES, INC.
To: EXOCURE SWEDEN AB
Reel/Frame 064189/0174 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 25, 2022
From: LÖTVALL, JAN; JANG, SU CHUL; CVJETKOVIC, ALEKSANDER; LASSER, CECILIA
To: EXOCURE BIOSCIENCES INC.
Reel/Frame 061528/0211 →
Priority Claims (1)
GB 1714890 · Sep 15, 2017 · national
Continuity (1)
Related Publication 20200249234A1 · Aug 6, 2020