3V86

Computational Design of a Protein Crystal

3V86 の概要

• エントリーDOI: 10.2210/pdb3v86/pdb
• 分子名称: De novo design helix (1 entity in total)
• 機能のキーワード: computational design of a protein crystal, helical coil, de novo designed helix, de novo protein
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 3171.64

構造登録者

Acharya, R.,North, B.,Saven, J.,DeGrado, W. (登録日: 2011-12-22, 公開日: 2012-05-09, 最終更新日: 2023-09-13)

主引用文献

Lanci, C.J.,Macdermaid, C.M.,Kang, S.G.,Acharya, R.,North, B.,Yang, X.,Qiu, X.J.,Degrado, W.F.,Saven, J.G.
Computational design of a protein crystal.
Proc.Natl.Acad.Sci.USA, 109:7304-7309, 2012

PubMed Abstract: Protein crystals have catalytic and materials applications and are central to efforts in structural biology and therapeutic development. Designing predetermined crystal structures can be subtle given the complexity of proteins and the noncovalent interactions that govern crystallization. De novo protein design provides an approach to engineer highly complex nanoscale molecular structures, and often the positions of atoms can be programmed with sub-Å precision. Herein, a computational approach is presented for the design of proteins that self-assemble in three dimensions to yield macroscopic crystals. A three-helix coiled-coil protein is designed de novo to form a polar, layered, three-dimensional crystal having the P6 space group, which has a "honeycomb-like" structure and hexameric channels that span the crystal. The approach involves: (i) creating an ensemble of crystalline structures consistent with the targeted symmetry; (ii) characterizing this ensemble to identify "designable" structures from minima in the sequence-structure energy landscape and designing sequences for these structures; (iii) experimentally characterizing candidate proteins. A 2.1 Å resolution X-ray crystal structure of one such designed protein exhibits sub-Å agreement [backbone root mean square deviation (rmsd)] with the computational model of the crystal. This approach to crystal design has potential applications to the de novo design of nanostructured materials and to the modification of natural proteins to facilitate X-ray crystallographic analysis.

PubMed: 22538812
DOI: 10.1073/pnas.1112595109

実験手法

X-RAY DIFFRACTION (2.91 Å)