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Membrane-Mediated Cooperative Interactions of CD47 and SIRPα
Li L(李龙); Gui, Chen; Hu, Jinglei; Rozycki, Bartosz
Corresponding AuthorRozycki, Bartosz([email protected])
Source PublicationMEMBRANES
2023-11-01
Volume13Issue:11Pages:13
AbstractThe specific binding of the ubiquitous 'marker of self' protein CD47 to the SIRP alpha protein anchored in the macrophage plasma membrane results in the inhibition of the engulfment of 'self' cells by macrophages and thus constitutes a key checkpoint of our innate immune system. Consequently, the CD47-SIRP alpha protein complex has been recognized as a potential therapeutic target in cancer and inflammation. Here, we introduce a lattice-based mesoscale model for the biomimetic system studied recently in fluorescence microscopy experiments where GFP-tagged CD47 proteins on giant plasma membrane vesicles bind to SIRP alpha proteins immobilized on a surface. Computer simulations of the lattice-based mesoscale model allow us to study the biomimetic system on multiple length scales, ranging from single nanometers to several micrometers and simultaneously keep track of single CD47-SIRP alpha binding and unbinding events. Our simulations not only reproduce data from the fluorescence microscopy experiments but also are consistent with results of several other experiments, which validates our numerical approach. In addition, our simulations yield quantitative predictions on the magnitude and range of effective, membrane-mediated attraction between CD47-SIRP alpha complexes. Such detailed information on CD47-SIRP alpha interactions cannot be obtained currently from experiments alone. Our simulation results thus extend the present understanding of cooperative effects in CD47-SIRP alpha interactions and may have an influence on the advancement of new cancer treatments.
Keywordmembrane adhesion biomimetics computer simulations CD47 SIRP alpha
DOI10.3390/membranes13110871
Indexed BySCI ; EI
Language英语
WOS IDWOS:001114541400001
WOS KeywordRECEPTOR-LIGAND BINDING ; ANCHORED RECEPTORS ; AGGREGATION ; ADHESION ; PROTEINS ; ENHANCE
WOS Research AreaBiochemistry & Molecular Biology ; Chemistry ; Engineering ; Materials Science ; Polymer Science
WOS SubjectBiochemistry & Molecular Biology ; Chemistry, Physical ; Engineering, Chemical ; Materials Science, Multidisciplinary ; Polymer Science
Funding ProjectNational Science Centre of Poland[2021/40/Q/NZ1/00017] ; National Natural Science Foundation of China[12232019] ; National Natural Science Foundation of China[12272388] ; National Natural Science Foundation of China[21973040] ; National Natural Science Foundation of China[22161132012] ; Youth Innovation Promotion Association of the Chinese Academy of Sciences
Funding OrganizationNational Science Centre of Poland ; National Natural Science Foundation of China ; Youth Innovation Promotion Association of the Chinese Academy of Sciences
Classification二类
Ranking1
ContributorRozycki, Bartosz
Citation statistics
Cited Times:4[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://dspace.imech.ac.cn/handle/311007/93558
Collection非线性力学国家重点实验室
Recommended Citation
GB/T 7714
Li L,Gui, Chen,Hu, Jinglei,et al. Membrane-Mediated Cooperative Interactions of CD47 and SIRPα[J]. MEMBRANES,2023,13,11,:13.Rp_Au:Rozycki, Bartosz
APA 李龙,Gui, Chen,Hu, Jinglei,&Rozycki, Bartosz.(2023).Membrane-Mediated Cooperative Interactions of CD47 and SIRPα.MEMBRANES,13(11),13.
MLA 李龙,et al."Membrane-Mediated Cooperative Interactions of CD47 and SIRPα".MEMBRANES 13.11(2023):13.
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