3RFJ
Design of a binding scaffold based on variable lymphocyte receptors of jawless vertebrates by module engineering
3RFJ の概要
| エントリーDOI | 10.2210/pdb3rfj/pdb |
| 関連するPDBエントリー | 3RFS |
| 分子名称 | Internalin B, repeat modules, Variable lymphocyte receptor, SULFATE ION (3 entities in total) |
| 機能のキーワード | lrr, protein binding, plasma |
| 由来する生物種 | Listeria monocytogenes (marine lamprey) 詳細 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 31419.40 |
| 構造登録者 | |
| 主引用文献 | Lee, S.C.,Park, K.,Han, J.,Lee, J.J.,Kim, H.J.,Hong, S.,Heu, W.,Kim, Y.J.,Ha, J.S.,Lee, S.G.,Cheong, H.K.,Jeon, Y.H.,Kim, D.,Kim, H.S. Design of a binding scaffold based on variable lymphocyte receptors of jawless vertebrates by module engineering Proc.Natl.Acad.Sci.USA, 109:3299-3304, 2012 Cited by PubMed Abstract: Repeat proteins have recently been of great interest as potential alternatives to immunoglobulin antibodies due to their unique structural and biophysical features. We here present the development of a binding scaffold based on variable lymphocyte receptors, which are nonimmunoglobulin antibodies composed of Leucine-rich repeat modules in jawless vertebrates, by module engineering. A template scaffold was first constructed by joining consensus repeat modules between the N- and C-capping motifs of variable lymphocyte receptors. The N-terminal domain of the template scaffold was redesigned based on the internalin-B cap by analyzing the modular similarity between the respective repeat units using a computational approach. The newly designed scaffold, termed "Repebody," showed a high level of soluble expression in bacteria, displaying high thermodynamic and pH stabilities. Ease of molecular engineering was shown by designing repebodies specific for myeloid differentiation protein-2 and hen egg lysozyme, respectively, by a rational approach. The crystal structures of designed repebodies were determined to elucidate the structural features and interaction interfaces. We demonstrate general applicability of the scaffold by selecting repebodies with different binding affinities for interleukin-6 using phage display. PubMed: 22328160DOI: 10.1073/pnas.1113193109 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.78 Å) |
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