100% satisfaction guarantee Immediately available after payment Both online and in PDF No strings attached
logo-home
Summary of the examination article $7.05   Add to cart

Summary

Summary of the examination article

 73 views  5 purchases
  • Course
  • Institution

Summary of the examination article 'Proteome profiling of whole plasma and plasma-derived extracellular vesicles facilitates the detection of tissue biomarkers in the non-obese diabetic mouse'.

Last document update: 11 months ago

Preview 2 out of 5  pages

  • November 27, 2023
  • November 27, 2023
  • 5
  • 2023/2024
  • Summary
avatar-seller
Summary paper: proteome profiling of
whole plasma and plasma derived EC
vesicles facilitates the detection of tissue
biomarkers in the non-obese diabetic
mouse (NOB)
T1D (type 1 diabets) -> loss of beta cells that produces insuline
 appearance of autoantibodies to beta cell antigens -> initiation of auto-immune reaction that can
lead to beta cell destruction (hyperglycemia)  T1D

C-peptide can be measured to evaluate the insulin production (will be cleaved of proinsulin and
secreted together with insulin)
-> if C-peptide, produced by beta cell, could be detected in the blood -> other proteins could also be
detected and could indicate the progression of the disease?

Proteomic analysis of blood plasma using MS is used for the discovery of protein biomarkers:
Protein biomarkers are useful in type 1 diabetes T1D: presence, progression and severity of the
disease
-> detection of new biomarkers that could give insights in disease phenotypes

Samples of non-obese diabetic mouse -> integrated proteome analysis could be useful for the
discovery of new endotype specific biomarkers in T1D

Why enrichment of EC vesicles?
 It may improve the detection and identification of low abundance biomarkers
 EC vesicles
o Small phospholipid bilayer membrane-bound vesicles -> secreted by all cell types in
EC space
o They contain DNA, RNA and proteins from their parent cell
o Function in IC communication
 EC vesicles subtypes: size/ pathway
o Exosomes: endocytotic pathway (nm)
o Microvesicles: by budding of plasma membrane (nm)
o Apoptotic bodies: apoptotic pathway (mm)

Isolation of EC vesicles: based on sample volume
 Differential ultracentrifugation
o Limitations: expensive, co-purification of protein aggregates, long processing time
o Separate exosomes and microvesicles
 Size exclusion chromatography (SEC)
o qEV
 Immunoprecipitation
 Membrane affinity (MA)
o ExoEasy




1

, GOAL
Develop a protocol for improved detection of tissue-enriched proteins in plasma samples from an
experimental model of T1D, the NOD mouse.

In this study, they wanted to look whether the combined analysis of whole plasma samples and
plasma-derived EC vesicles fractions increased the number of unique proteins identified by mass
spectrometry (MS) compared to the analysis of whole plasma samples alone

Result: 600 proteins were detected in EC vesicles enriched samples -> >1/3 of these proteins were
not found in the whole plasma sample
 parallel profiling of EV-enriched plasma fractions and whole plasma samples increases the
overall proteome depth and facilitates the discovery of tissue-enriched proteins in plasma

Methods
2 methods based on the EC vesicles enrichment
 SEC (qEV)
 MA (exoEasy)

exoEasy
1. Filter the plasma -> remove large particles
2. Mix plasma with XBP buffer
3. Add plasma to exoEasy spin column -> spin
4. Wash the bound exosomes with XWP -> spin
5. Elute the exosomes by adding XE buffer
6. Incubation
7. Spin -> collect elute
8. Elute is reapplied to the column membrane -> incubation
9. Spin and collect the final elute

qEV
1. Filter the plasma
2. Load the plasma on qEV column
3. Fractions of 0,5ml were collected and analyzed for protein, particle content -> identify the
optimal fractions for EV collection

qEV: fraction 7-15 were collected




-> Transmission electron microscopy
-> Nanoparticle tracking analysis -> measure the protein concentration and size distribution
-> Depletion of abundant plasma proteins


2

The benefits of buying summaries with Stuvia:

Guaranteed quality through customer reviews

Guaranteed quality through customer reviews

Stuvia customers have reviewed more than 700,000 summaries. This how you know that you are buying the best documents.

Quick and easy check-out

Quick and easy check-out

You can quickly pay through credit card or Stuvia-credit for the summaries. There is no membership needed.

Focus on what matters

Focus on what matters

Your fellow students write the study notes themselves, which is why the documents are always reliable and up-to-date. This ensures you quickly get to the core!

Frequently asked questions

What do I get when I buy this document?

You get a PDF, available immediately after your purchase. The purchased document is accessible anytime, anywhere and indefinitely through your profile.

Satisfaction guarantee: how does it work?

Our satisfaction guarantee ensures that you always find a study document that suits you well. You fill out a form, and our customer service team takes care of the rest.

Who am I buying these notes from?

Stuvia is a marketplace, so you are not buying this document from us, but from seller AVL2. Stuvia facilitates payment to the seller.

Will I be stuck with a subscription?

No, you only buy these notes for $7.05. You're not tied to anything after your purchase.

Can Stuvia be trusted?

4.6 stars on Google & Trustpilot (+1000 reviews)

78075 documents were sold in the last 30 days

Founded in 2010, the go-to place to buy study notes for 14 years now

Start selling
$7.05  5x  sold
  • (0)
  Add to cart