Molecular modelling showed optimal fit between TSR5 in trimeric properdin and C345C in the C3b moiety for stabilization of the alternative convertase, whereas binding to molecular patterns in myeloperoxidase, endothelial cells and Neisseria meningitides was indirectly mediated by initial C3 activation

Morten Harboe,Christina Johnson,Stig Nymo,Karin Ekholt,Camilla Schjalm,Julie Katrine Lindstad,Anne Pharo,Bernt Christian Hellerud,Kristina Nilsson Ekdahl,Tom Eirik Mollnes,Per H. Nilsson

IMMUNOBIOLOGY（2016）

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摘要

Molecular modelling showed optimal fit between TSR5 in trimeric properdin and C345C in the C3b moiety for stabilization of the alternative convertase, whereas binding to molecular patterns in myeloperoxidase, endothelial cells and Neisseria meningitides was indirectly mediated by initial C3 activation

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