دورية أكاديمية

Molecular mechanism of complement inhibition by the trypanosome receptor ISG65

التفاصيل البيبلوغرافية
العنوان: Molecular mechanism of complement inhibition by the trypanosome receptor ISG65
المؤلفون: Alexander D Cook, Mark Carrington, Matthew K Higgins
المصدر: eLife, Vol 12 (2024)
بيانات النشر: eLife Sciences Publications Ltd, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine
LCC:Science
LCC:Biology (General)
مصطلحات موضوعية: trypanosome, complement, C3, ISG65, Medicine, Science, Biology (General), QH301-705.5
الوصف: African trypanosomes replicate within infected mammals where they are exposed to the complement system. This system centres around complement C3, which is present in a soluble form in serum but becomes covalently deposited onto the surfaces of pathogens after proteolytic cleavage to C3b. Membrane-associated C3b triggers different complement-mediated effectors which promote pathogen clearance. To counter complement-mediated clearance, African trypanosomes have a cell surface receptor, ISG65, which binds to C3b and which decreases the rate of trypanosome clearance in an infection model. However, the mechanism by which ISG65 reduces C3b function has not been determined. We reveal through cryogenic electron microscopy that ISG65 has two distinct binding sites for C3b, only one of which is available in C3 and C3d. We show that ISG65 does not block the formation of C3b or the function of the C3 convertase which catalyses the surface deposition of C3b. However, we show that ISG65 forms a specific conjugate with C3b, perhaps acting as a decoy. ISG65 also occludes the binding sites for complement receptors 2 and 3, which may disrupt recruitment of immune cells, including B cells, phagocytes, and granulocytes. This suggests that ISG65 protects trypanosomes by combining multiple approaches to dampen the complement cascade.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2050-084X
العلاقة: https://elifesciences.org/articles/88960Test; https://doaj.org/toc/2050-084XTest
DOI: 10.7554/eLife.88960
الوصول الحر: https://doaj.org/article/6730aab5a1254415b53e756fbdf4bda6Test
رقم الانضمام: edsdoj.6730aab5a1254415b53e756fbdf4bda6
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:2050084X
DOI:10.7554/eLife.88960