Nanobodies Provide Insight into the Molecular Mechanisms of the Complement Cascade and Offer New Therapeutic Strategies

被引:6
|
作者
Zarantonello, Alessandra [1 ]
Pedersen, Henrik [1 ]
Laursen, Nick S. [2 ]
Andersen, Gregers R. [1 ]
机构
[1] Aarhus Univ, Dept Mol Biol & Genet, DK-8000 Aarhus, Denmark
[2] Aarhus Univ, Dept Biomed, DK-8000 Aarhus, Denmark
关键词
complement system; proteolytic cascade; convertase; inhibitor; structural biology; molecular mechanism; C3-SPECIFIC NANOBODY; ALTERNATIVE PATHWAY; ACTIVATION; CONVERTASES; PROPERDIN; EVOLUTION; PROTEIN; C2; C4;
D O I
10.3390/biom11020298
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The complement system is part of the innate immune response, where it provides immediate protection from infectious agents and plays a fundamental role in homeostasis. Complement dysregulation occurs in several diseases, where the tightly regulated proteolytic cascade turns offensive. Prominent examples are atypical hemolytic uremic syndrome, paroxysmal nocturnal hemoglobinuria and Alzheimer's disease. Therapeutic intervention targeting complement activation may allow treatment of such debilitating diseases. In this review, we describe a panel of complement targeting nanobodies that allow modulation at different steps of the proteolytic cascade, from the activation of the C1 complex in the classical pathway to formation of the C5 convertase in the terminal pathway. Thorough structural and functional characterization has provided a deep mechanistic understanding of the mode of inhibition for each of the nanobodies. These complement specific nanobodies are novel powerful probes for basic research and offer new opportunities for in vivo complement modulation.
引用
收藏
页码:1 / 24
页数:23
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