Complement component 1r
Complement component 1r (C1r) is a protein involved in the complement system, which is an integral part of the immune system that enhances (complements) the ability of antibodies and phagocytic cells to clear pathogens from an organism. C1r is a serine protease that is part of the C1 complex, which also includes C1q and C1s. The C1 complex is the first component of the classical pathway of the complement system.
Structure[edit | edit source]
C1r is a modular enzyme composed of several regions: two CUB domains (C1r/C1s, Uegf, Bmp1), two EGF-like domains, a CCP (complement control protein) domain, and the serine protease domain. This structure is essential for its interaction with C1q and C1s, and for its enzymatic activity.
Function[edit | edit source]
Upon activation by C1q binding to antibodies that are themselves bound to antigens, C1r is auto-activated through a cleavage that occurs in its serine protease domain. Activated C1r then cleaves and activates C1s, another serine protease, which subsequently leads to the activation of the complement cascade. This cascade results in several immune responses, including opsonization, cell lysis, and inflammation.
Regulation[edit | edit source]
The activity of C1r is tightly regulated to prevent spontaneous activation of the complement system, which could lead to tissue damage. C1 inhibitor (C1-INH) is a key regulator that binds to activated C1r (and C1s), inhibiting its protease activity and preventing further activation of the complement system.
Clinical Significance[edit | edit source]
Deficiencies or dysfunctions in C1r can lead to immune system-related diseases. For example, a deficiency in C1-INH can result in hereditary angioedema, characterized by sudden and severe swelling in various parts of the body. Additionally, excessive activation of C1r has been implicated in autoimmune diseases, where the immune system attacks the body's own tissues.
Research[edit | edit source]
Research into C1r focuses on understanding its structure-function relationships, its role in disease, and its potential as a therapeutic target. Inhibitors of C1r are being explored as treatments for conditions involving excessive complement activation, such as certain autoimmune diseases and ischemia-reperfusion injury.
See Also[edit | edit source]
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD's Wellness Encyclopedia |
Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD