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Related Concept Videos

Complement System01:27

Complement System

10.6K
The complement system is a group of approximately 20 plasma proteins that strengthen the body's defenses against infections through opsonization, inflammation, and cell lysis. Opsonization involves coating pathogens with complement proteins, making them more recognizable and facilitating phagocyte engulfment. Certain complement proteins induce inflammation that attracts immune cells to the site of infection. Cell lysis involves the destruction of pathogens through the formation of a...
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Blood Studies for Cardiovascular System I: Cardiac Biomarkers01:20

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Cardiac biomarkers are enzymes, proteins, and hormones released into the blood when cardiac cells are injured. They are powerful tools for triaging.
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Related Experiment Video

Updated: May 2, 2026

Analyzing Dynamic Protein Complexes Assembled On and Released From Biolayer Interferometry Biosensor Using Mass Spectrometry and Electron Microscopy
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Analyzing Dynamic Protein Complexes Assembled On and Released From Biolayer Interferometry Biosensor Using Mass Spectrometry and Electron Microscopy

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Membrane attack complex generation increases as a function of time in stored blood.

X Hu1, R P Patel, J A Weinberg

  • 1Department of Microbiology.

Transfusion Medicine (Oxford, England)
|March 5, 2014
PubMed
Summary

The complement system

Keywords:
complementextrinsic protease pathwaymembrane attack complex

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Area of Science:

  • Immunology
  • Transfusion Medicine
  • Hematology

Background:

  • Red blood cells (RBCs) undergo changes during storage, potentially causing adverse transfusion outcomes.
  • Complement activation during leukodepletion and storage may contribute to the RBC storage lesion.

Purpose of the Study:

  • To investigate the role of the complement system in red blood cell (RBC) hemolysis during storage.
  • To determine if complement activation contributes to the RBC storage lesion.

Main Methods:

  • Cross-sectional analysis of leukoreduced RBC units stored for 1-6 weeks.
  • Quantification of complement activation products (C3a, C5a, Bb, iC3b, C4d, C5b-9/MAC) using ELISA.

Main Results:

  • Membrane attack complex (MAC) levels significantly increased in RBC units with extended storage time.
  • C5b-9 deposition on RBCs also increased as a function of storage duration.

Conclusions:

  • The terminal complement pathway, specifically MAC formation, is a primary contributor to RBC changes during storage.
  • Inhibiting the terminal complement pathway could stabilize RBCs and extend their shelf life.