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DOI | 10.1073/pnas.2102787118 |
C1q binding to surface-bound IgG is stabilized by C1r2s2 proteases | |
Zwarthoff S.A.; Widmer K.; Kuipers A.; Strasser J.; Ruyken M.; Aerts P.C.; de Haas C.J.C.; Ugurlar D.; den Boer M.A.; Vidarsson G.; van Strijp J.A.G.; Gros P.; Parren P.W.H.I.; van Kessel K.P.M.; Preiner J.; Beurskens F.J.; Schuurman J.; Ricklin D.; Rooijakkers S.H.M. | |
发表日期 | 2021 |
ISSN | 0027-8424 |
卷号 | 118期号:26 |
英文摘要 | Complement is an important effector mechanism for antibodymediated clearance of infections and tumor cells. Upon binding to target cells, the antibody's constant (Fc) domain recruits complement component C1 to initiate a proteolytic cascade that generates lytic pores and stimulates phagocytosis. The C1 complex (C1qr2s2) consists of the large recognition protein C1q and a heterotetramer of proteases C1r and C1s (C1r2s2). While interactions between C1 and IgG-Fc are believed to be mediated by the globular heads of C1q, we here find that C1r2s2 proteases affect the capacity of C1q to form an avid complex with surface-bound IgG molecules (on various 2,4-dinitrophenol [DNP]-coated surfaces and pathogenic Staphylococcus aureus). The extent to which C1r2s2 contributes to C1q-IgG stability strongly differs between human IgG subclasses. Using antibody engineering of monoclonal IgG, we reveal that hexamer-enhancing mutations improve C1q-IgG stability, both in the absence and presence of C1r2s2. In addition, hexamer-enhanced IgGs targeting S. aureus mediate improved complement-dependent phagocytosis by human neutrophils. Altogether, these molecular insights into complement binding to surface-bound IgGs could be important for optimal design of antibody therapies. © 2021 National Academy of Sciences. All rights reserved. |
英文关键词 | C1; Complement; IgG hexamerization; IgG subclasses; Staphylococcus aureus |
语种 | 英语 |
来源期刊 | Proceedings of the National Academy of Sciences of the United States of America
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文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/238881 |
作者单位 | Medical Microbiology, University Medical Center Utrecht, Utrecht University, Utrecht, 3584 CX, Netherlands; Pharmaceutical Sciences, University of Basel, Basel, 4001, Switzerland; Nano Structuring and Bio-Analytics Group, TIMed Center of Applied Sciences Upper Austria, Linz, 4020, Austria; Structural Biochemistry, Bijvoet Center for Biomolecular Research, Utrecht University, Utrecht, 3584 CH, Netherlands; Biomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, 3584 CH, Netherlands; Netherlands Proteomics Center, Utrecht, 3584 CH, Netherlands; Experimental Immunohematology, Sanquin Research, Amsterdam, 1066 CX, Netherlands; Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, 2333 ZA, Netherlands; Lava Therapeutics, Utrecht, 3584 CM, Netherlands; Genmab, Utrecht, 3584 CT, Netherlands |
推荐引用方式 GB/T 7714 | Zwarthoff S.A.,Widmer K.,Kuipers A.,et al. C1q binding to surface-bound IgG is stabilized by C1r2s2 proteases[J],2021,118(26). |
APA | Zwarthoff S.A..,Widmer K..,Kuipers A..,Strasser J..,Ruyken M..,...&Rooijakkers S.H.M..(2021).C1q binding to surface-bound IgG is stabilized by C1r2s2 proteases.Proceedings of the National Academy of Sciences of the United States of America,118(26). |
MLA | Zwarthoff S.A.,et al."C1q binding to surface-bound IgG is stabilized by C1r2s2 proteases".Proceedings of the National Academy of Sciences of the United States of America 118.26(2021). |
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