5VL7

PCSK9 complex with Fab33

5VL7 の概要

• エントリーDOI: 10.2210/pdb5vl7/pdb
• 分子名称: Proprotein convertase subtilisin/kexin type 9, Fab33 heavy chain, Fab33 light chain, ... (4 entities in total)
• 機能のキーワード: immunoglobulin proprotein convertase, subtilisin, hydrolase
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 123017.27

構造登録者

Eigenbrot, C.,Shia, S. (登録日: 2017-04-25, 公開日: 2017-08-16, 最終更新日: 2024-10-23)

主引用文献

Zhang, Y.,Ultsch, M.,Skelton, N.J.,Burdick, D.J.,Beresini, M.H.,Li, W.,Kong-Beltran, M.,Peterson, A.,Quinn, J.,Chiu, C.,Wu, Y.,Shia, S.,Moran, P.,Di Lello, P.,Eigenbrot, C.,Kirchhofer, D.
Discovery of a cryptic peptide-binding site on PCSK9 and design of antagonists.
Nat. Struct. Mol. Biol., 24:848-856, 2017

PubMed Abstract: Proprotein convertase subtilisin/kexin type 9 (PCSK9) regulates plasma LDL cholesterol (LDL-c) levels by promoting the degradation of liver LDL receptors (LDLRs). Antibodies that inhibit PCSK9 binding to the EGF(A) domain of the LDLR are effective in lowering LDL-c. However, the discovery of small-molecule therapeutics is hampered by difficulty in targeting the relatively flat EGF(A)-binding site on PCSK9. Here we demonstrate that it is possible to target this site, based on the finding that the PCSK9 P' helix displays conformational flexibility. As a consequence, the vacated N-terminal groove of PCSK9, which is adjacent to the EGF(A)-binding site, is in fact accessible to small peptides. In phage-display experiments, the EGF(A)-mimicking peptide Pep2-8 was used as an anchor peptide for the attachment of an extension peptide library directed toward the groove site. Guided by structural information, we further engineered the identified groove-binding peptides into antagonists, which encroach on the EGF(A)-binding site and inhibit LDLR binding.

PubMed: 28825733
DOI: 10.1038/nsmb.3453

実験手法

X-RAY DIFFRACTION (3.5 Å)