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9DZE

Computationally Designed Bifaceted Protein Nanomaterial pD5-14

9DZE の概要
エントリーDOI10.2210/pdb9dze/pdb
EMDBエントリー47327
分子名称pD5-14 A component, pD5-14 B component, pD5-14 C component, ... (4 entities in total)
機能のキーワードnanomaterial, 4 component, bifaceted, penton, de novo protein
由来する生物種synthetic construct
詳細
タンパク質・核酸の鎖数30
化学式量合計1257930.97
構造登録者
Carr, K.D.,Borst, A.J.,Weidle, C. (登録日: 2024-10-16, 公開日: 2024-10-30, 最終更新日: 2024-11-13)
主引用文献Rankovic, S.,Carr, K.D.,Decarreau, J.,Skotheim, R.,Kibler, R.D.,Ols, S.,Lee, S.,Chun, J.,Tooley, M.,Dauparas, J.,Eisenach, H.E.,Glogl, M.,Weidle, C.,Borst, A.J.,Baker, D.,King, N.P.
Computational design of bifaceted protein nanomaterials with tailorable properties.
Biorxiv, 2024
Cited by
PubMed Abstract: Recent advances in computational methods have led to considerable progress in the design of self-assembling protein nanoparticles. However, nearly all nanoparticles designed to date exhibit strict point group symmetry, with each subunit occupying an identical, symmetrically related environment. This property limits the structural diversity that can be achieved and precludes anisotropic functionalization. Here, we describe a general computational strategy for designing multi-component bifaceted protein nanomaterials with two distinctly addressable sides. The method centers on docking pseudosymmetric heterooligomeric building blocks in architectures with dihedral symmetry and designing an asymmetric protein-protein interface between them. We used this approach to obtain an initial 30-subunit assembly with pseudo-D5 symmetry, and then generated an additional 15 variants in which we controllably altered the size and morphology of the bifaceted nanoparticles by designing extensions to one of the subunits. Functionalization of the two distinct faces of the nanoparticles with protein minibinders enabled specific colocalization of two populations of polystyrene microparticles coated with target protein receptors. The ability to accurately design anisotropic protein nanomaterials with precisely tunable structures and functions will be broadly useful in applications that require colocalizing two or more distinct target moieties.
PubMed: 39484564
DOI: 10.1101/2024.10.18.619149
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (4.3 Å)
構造検証レポート
Validation report summary of 9dze
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

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