The Evolution, Oligomerization, Function, and Action Mechanism of α2-Macroglobulin
Wenshuo Xie, Lili Gao, Hongkuan Deng, Dongwu Liu, Qiuxiang Pang

TL;DR
This paper reviews the evolution, structure, and diverse functions of α2-Macroglobulin, a key protein involved in immune and inflammatory responses.
Contribution
The paper provides a comprehensive overview of A2M's evolutionary history and functional roles across species, highlighting its potential for clinical applications.
Findings
A2M is highly conserved across invertebrates and vertebrates, indicating its evolutionary significance.
A2M plays a central role in immune responses by inhibiting proteases and interacting with cytokines and receptors.
The protein's functional domains suggest broad therapeutic potential in disease treatment.
Abstract
α2-Macroglobulin (A2M), a large tetrameric glycoprotein with a molecular weight of approximately 720 kDa, is a key member of the α-macroglobulin superfamily. Its origin dates back 600–700 million years, positioning A2M as an evolutionary link within the α-macroglobulin family and complement components C3, C4, and C5. Structural predictions of A2M across different species reveal a remarkably high degree of conservation between invertebrates and vertebrates. A2M is abundantly present in the body fluids of both vertebrates and invertebrates, and its diverse biological functions are governed by five key functional domains within its molecular structure. The most well-established role of A2M is the entrapment and inhibition of proteases. Beyond that, it interacts with cytokines, growth factors, and membrane receptors, thereby playing a broad role in immune and inflammatory responses,…
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Taxonomy
TopicsInvertebrate Immune Response Mechanisms · Complement system in diseases · Protease and Inhibitor Mechanisms
