Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Methods of detecting therapeutic exosomes

An exosome, detection table technology, applied in the fields of molecular biology and genetics, cell biology, medicine, can solve the problem that the molecular or biochemical basis has not been elucidated

Inactive Publication Date: 2017-08-29
AGENCY FOR SCI TECH & RES
View PDF13 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

To date, most bioefficacy studies have been limited to the immune response of immune cells to exosomes, especially dendritic cells 2 , but the molecular or biochemical basis of these biological responses has not been elucidated

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Methods of detecting therapeutic exosomes
  • Methods of detecting therapeutic exosomes
  • Methods of detecting therapeutic exosomes

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0334] Example 1. Materials and Methods - Preparation of Exosomes Exosomes

[0335] Exosomes were purified from huES9.E1 -derived MSC conditioned cultures (CM) using HPLC as previously described. Briefly, CM collected from MSC cultures was concentrated 50-fold by tangential flow filtration (TFF) using membranes with 100 kDa MWCO (Sartorius, Goettingen, Germany).

[0336] Then, CM was passed through a chromatography column (TSK Guard column SWXL, 6x40mm and TSK gel G4000SWXL, 7.8x300mm, Tosoh Corp., Tokyo, Japan).

[0337] Exosomes were collected from the first peak of elution and concentrated using 100 kDa MWCO filters (Sartorius). Filter exosomes with a 0.22 µm filter before storage or use.

Embodiment 2

[0338] Example 2. Materials and methods - LC MS / MS

[0339] Proteins in 2 ml dialyzed exosomes were reduced, alkylated and trypsinized as described (20).

[0340] Then, the samples were desalted by passing the digestion mixture through a conditioned Sep-Pak C-18SPE kit (Waters, Milford, MA, USA) with 3% acetonitrile (ACN) (New JT Baker, Phillipsburg, NJ) and 0.1% Wash twice with formic acid (FA) buffer and elute with 70% ACN and 0.1% FA buffer.

[0341] Eluted samples were then dried to approximately 10% of their original volume by removing the organic solvent in a vacuum centrifuge.

[0342] To reduce sample complexity, offline peptide fractionation was performed with an HPLC system (Shimadzu, Japan) through a Polysulfoethyl SCX column (200mm×4.6mm) (PolyLC, USA).

[0343] 1ml / min, mobile phase A (5mM KH 4 PO 4 +30% acetonitrile) and mobile phase B (5mM KH 4 PO 4 + 30% acetonitrile + 350 mM KCl).

[0344] Collect and dry into 8 fractions in a vacuum centrifuge.

[034...

Embodiment 3

[0354] Example 3. Materials and Methods - Antibody Chips

[0355] According to the manufacturer's instructions, use a Biotin-labeled Human Antibody Chip I (RayBio, Norcross, GA) detected the presence of cytokines and other proteins from 500 l of unconditioned cultures and exosomes from three independent preparations.

[0356] Exosomes Cytokines and other proteins were considered present in exosomes if the signal intensity was 2-fold higher (p<0.05) compared to non-conditioned cultures.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

We describe a method of detecting a therapeutic exosome, the method comprising detecting an activity of an exosome. The activity may be selected from the group consisting of: (a) immunodulatory activity; (b) complement inhibition activity; (c) proteasome activity; (d) glycolytic enzyme activity; (e) anti-oxidative activity; (f) extracellular matrix (ECM) modifying activity; (g) NT5E (CD73) ecto-5'-ectonucleotidase activity; (h) ion homeostasis activity; and (i) chaperone activity. If the exosome is detected as having one or more such activities, the exosome is likely to comprise a therapeutic exosome having therapeutic activity.

Description

[0001] This application is a divisional application of the Chinese patent application with the application number 201280017773.X, the application date is February 10, 2012, and the invention title is "Method for Detecting Therapeutic Exosomes". technical field [0002] The present invention relates to the fields of medicine, cell biology, molecular biology and genetics. The present invention relates to the field of medicine. Background technique [0003] Exosomes were once thought of as cells' "garbage bags" for discarding unwanted proteins 1 . However, exosomes are increasingly recognized to have important physiological functions, especially in cellular communication. [0004] Exosomes are 50-100ηm double lipid membrane vesicles secreted by many cell types 2 . They belong to a class of secreted cellular products called microsomes, which broadly encompasses all secreted membrane vesicles. In addition to exosomes, microparticles also include microvesicles (100-1000 ηm), ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): G01N33/50G01N33/68
CPCG01N33/5005G01N33/68G01N33/6848G01N2570/00A61P11/00A61P11/02A61P17/00A61P17/02A61P17/06A61P25/16A61P25/28A61P29/00A61P35/00A61P37/02A61P37/08A61P9/00A61P9/10A61P3/10
Inventor 林赛娟
Owner AGENCY FOR SCI TECH & RES
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com