3T4A

Structure of a truncated form of Staphylococcal Complement Inhibitor B bound to human C3c at 3.4 Angstrom resolution

3T4A の概要

• エントリーDOI: 10.2210/pdb3t4a/pdb
• 関連するPDBエントリー: 3T46 3T47 3T48 3T49
• 分子名称: Complement C3 beta chain, Complement C3c alpha' chain fragment 1, Complement C3c alpha' chain fragment 2, ... (4 entities in total)
• 機能のキーワード: age-related macular degeneration, cleavage on pair of basic residues, complement alternate pathway, complement pathway, disease mutation, disulfide bond, glycoprotein, hemolytic uremic syndrome, immunity, inflammatory response, innate immunity, phosphoprotein, secreted, thioester bond, immune system
• 由来する生物種: Staphylococcus aureus subsp. aureus; 詳細
• 細胞内の位置: Secreted: P01024 P01024 P01024
• タンパク質・核酸の鎖数: 8
• 化学式量合計: 285532.87

構造登録者

Garcia, B.L.,Geisbrecht, B.V.,Summers, B.J. (登録日: 2011-07-25, 公開日: 2011-11-23, 最終更新日: 2024-11-06)

主引用文献

Garcia, B.L.,Summers, B.J.,Lin, Z.,Ramyar, K.X.,Ricklin, D.,Kamath, D.V.,Fu, Z.Q.,Lambris, J.D.,Geisbrecht, B.V.
Diversity in the C3b Convertase Contact Residues and Tertiary Structures of the Staphylococcal Complement Inhibitor (SCIN) Protein Family.
J.Biol.Chem., 287:628-640, 2012

PubMed Abstract: To survive in immune-competent hosts, the pathogen Staphylococcus aureus expresses and secretes a sophisticated array of proteins that inhibit the complement system. Among these are the staphylococcal complement inhibitors (SCIN), which are composed of three active proteins (SCIN-A, -B, and -C) and one purportedly inactive member (SCIN-D or ORF-D). Because previous work has focused almost exclusively on SCIN-A, we sought to provide initial structure/function information on additional SCIN proteins. To this end we determined crystal structures of an active, N-terminal truncation mutant of SCIN-B (denoted SCIN-B18-85) both free and bound to the C3c fragment of complement component C3 at 1.5 and 3.4 Å resolution, respectively. Comparison of the C3c/SCIN-B18-85 structure with that of C3c/SCIN-A revealed that both proteins target the same functional hotspot on the C3b/C3c surface yet harbor diversity in both the type of residues and interactions formed at their C3b/C3c interfaces. Most importantly, these structures allowed identification of Arg44 and Tyr51 as residues key for SCIN-B binding to C3b and subsequent inhibition of the AP C3 convertase. In addition, we also solved several crystal structures of SCIN-D to 1.3 Å limiting resolution. This revealed an unexpected structural deviation in the N-terminal α helix relative to SCIN-A and SCIN-B. Comparative analysis of both electrostatic potentials and surface complementarity suggest a physical explanation for the inability of SCIN-D to bind C3b/C3c. Together, these studies provide a more thorough understanding of immune evasion by S. aureus and enhance potential use of SCIN proteins as templates for design of complement targeted therapeutics.

PubMed: 22086928
DOI: 10.1074/jbc.M111.298984

実験手法

X-RAY DIFFRACTION (3.4 Å)