Related Experiment Video
Updated: Jul 19, 2026

Measuring the 50% Haemolytic Complement (CH50) Activity of Serum
Published on: March 29, 2010
Steady state approximation in the minimal model of the alternative pathway of complement
1Department of Chemistry, Williams College, Williamstown, MA 01267, USA.
Abstract:
Complement is a response mechanism of the immune system. Two initiation pathways have been characterized for complement. The classical pathway is antibody mediated while the alternative pathway is not. Since the alternative pathway is independent of antibodies, it is always active. For the alternative pathway we have previously developed a minimal model. Using parameters within physiological bounds, the model showed complex behavior also within physiological bounds. Thus the model seems to be an appropriate representation of the alternative pathway response. By applying a steady state assumption to the Michaelis Menten step of the minimal model, we reduce the number of variables from six to five. A comparison between the dynamics of the minimal and contracted models reveals that the two descriptions may not be compatible. Although both systems show chaotic behavior it occurs in different regions of parameter space.
More Related Videos
09:27Functional Complementation Analysis (FCA): A Laboratory Exercise Designed and Implemented to Supplement the Teaching of Biochemical Pathways
Published on: June 24, 2016
07:26High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
Published on: July 18, 2017
Related Concept Videos
Reaction Mechanisms: The Steady-State Approximation
Complement System
Reaction Mechanisms: Rate-limiting Step Approximation
The Small x Assumption
Mechanistic Models: Compartment Models in Individual and Population Analysis
Pharmacokinetic Models: Comparison and Selection Criterion
Physiological models take a detailed approach by considering specific molecular processes. They can predict drug distribution, metabolism, and elimination changes, providing a comprehensive understanding of how drugs interact with the body.