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Updated: Jul 12, 2025

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Measurement of Factor V Activity in Human Plasma Using a Microplate Coagulation Assay
Published on: September 9, 2012
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Biology of factor XI
Samantha A Moellmer1, Cristina Puy1, Owen J T McCarty1
1Department of Biomedical Engineering, Oregon Health & Science University, Portland, OR.
Blood
|October 24, 2023
Summary
Coagulation Factor XI (FXI), originating from gene duplication, has a unique structure critical for blood clotting and other functions. Understanding FXI
Area of Science:
- Hemostasis and Thrombosis Research
- Molecular Biology of Blood Coagulation
- Evolutionary Genetics of Proteins
Background:
- Coagulation Factor XI (FXI) possesses a unique evolutionary origin via gene duplication of KLKB1, encoding plasma prekallikrein.
- Structurally, FXI is a homodimer with four apple and one catalytic domain, each with distinct binding affinities.
- FXI's role extends beyond coagulation to include barrier function, platelet activation, inflammation, and immune response.
Approach:
- This review critically examines the molecular biology of FXI.
- It details functional consequences at cellular, tissue, and organ levels.
- DNA mutations linked to FXI deficiency within each domain are highlighted.
Key Points:
- FXI acts as a molecular nexus for extrinsic and contact pathways, activating Factor IX to propagate thrombin generation.
- Each domain of FXI binds unique partners, regulating its conversion to a serine protease and substrate selectivity.
- Understanding FXI's structure-function is crucial for comprehending hemophilia C etiology.
Conclusions:
- A comprehensive understanding of FXI's domain structure-function is essential.
- This knowledge aids in understanding the etiology of hemophilia C.
- It also guides the identification of FXI regions for targeted inhibition of pathological functions without compromising physiological roles.
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