2LM5

Solution structure of Ca2+-CIB1 in complex with the cytoplasmic domain of the integrin aIIb subunit

2LM5 の概要

• エントリーDOI: 10.2210/pdb2lm5/pdb
• 関連するPDBエントリー: 1XO5 2L4H 2L4I
• NMR情報: BMRB: 18099
• 分子名称: Calcium and integrin-binding protein 1, CALCIUM ION (2 entities in total)
• 機能のキーワード: metal binding protein
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Membrane; Lipid-anchor: Q99828
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 24587.42

構造登録者

Huang, H.,Vogel, H.J. (登録日: 2011-11-22, 公開日: 2012-02-15, 最終更新日: 2024-05-15)

主引用文献

Huang, H.,Vogel, H.J.
Structural basis for the activation of platelet integrin alphaIIb-beta3 by calcium- and integrin-binding protein 1.
J.Am.Chem.Soc., 134:3864-3872, 2012

PubMed Abstract: Calcium and integrin binding protein 1 (CIB1) is a specific binding partner for the cytoplasmic domain of the αIIb subunit of the highly abundant platelet integrin αIIbβ3. This protein has been suggested to be involved in the regulation of the activation of αIIbβ3, a process leading to platelet aggregation and blood coagulation. In this work, the solution structure of the deuterated Ca(2+)-CIB1 protein complexed with an αIIb peptide was first determined through modern RDC-based NMR methods. Next, we generated a complex structure for CIB1 and the αIIb domain (Ca(2+)-CIB1/αIIb) using the program Haddock, which is based on experimental restraints obtained for the protein-peptide interface from cross-saturation NMR experiments. In this data-driven complex structure, the N-terminal α-helix of the cytoplasmic domain of αIIb is buried in the hydrophobic pocket of the C-lobe of Ca(2+)-CIB1. The C-terminal acidic tail of αIIb remains unstructured and likely interacts with several positively charged residues in the N-lobe of Ca(2+)-CIB1. A potential molecular mechanism for the CIB1-mediated activation of the platelet integrin could be proposed on the basis of the model structure of this protein complex. Another feature of this work is that, in the NMR cross-saturation experiments, we applied the selective radio frequency irradiation to the smaller binding partner (the αIIb peptide), and successfully detected the binding interface on the larger binding partner Ca(2+)-CIB1 through its selectively protonated methyl groups. This 'reverse' methodology has a broad potential to be employed to many other complexes where synthetic peptides and a suitably isotope-labeled medium- to large-sized protein are used to study protein-protein interactions.

PubMed: 22283712
DOI: 10.1021/ja2111306

実験手法

SOLUTION NMR