6YQX

Crystal structure of DeNovoTIM13, a de novo designed TIM barrel

6YQX の概要

• エントリーDOI: 10.2210/pdb6yqx/pdb
• 分子名称: de novo designed TIM barrel DeNovoTIM13, GLYCEROL, CHLORIDE ION, ... (4 entities in total)
• 機能のキーワード: de novo protein design, epistasis, stability landscape, tim barrel, (beta/alfa)8 barrel, de novo protein
• 由来する生物種: synthetic construct
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 22245.23

構造登録者

Romero-Romero, S.,Kordes, S.,Shanmugaratnam, S.,Fernandez-Velasco, D.A.,Hocker, B. (登録日: 2020-04-18, 公開日: 2021-07-21, 最終更新日: 2024-05-01)

主引用文献

Romero-Romero, S.,Costas, M.,Silva Manzano, D.A.,Kordes, S.,Rojas-Ortega, E.,Tapia, C.,Guerra, Y.,Shanmugaratnam, S.,Rodriguez-Romero, A.,Baker, D.,Hocker, B.,Fernandez-Velasco, D.A.
The Stability Landscape of de novo TIM Barrels Explored by a Modular Design Approach.
J.Mol.Biol., 433:167153-167153, 2021

PubMed Abstract: The ability to design stable proteins with custom-made functions is a major goal in biochemistry with practical relevance for our environment and society. Understanding and manipulating protein stability provide crucial information on the molecular determinants that modulate structure and stability, and expand the applications of de novo proteins. Since the (β/⍺)-barrel or TIM-barrel fold is one of the most common functional scaffolds, in this work we designed a collection of stable de novo TIM barrels (DeNovoTIMs), using a computational fixed-backbone and modular approach based on improved hydrophobic packing of sTIM11, the first validated de novo TIM barrel, and subjected them to a thorough folding analysis. DeNovoTIMs navigate a region of the stability landscape previously uncharted by natural TIM barrels, with variations spanning 60 degrees in melting temperature and 22 kcal per mol in conformational stability throughout the designs. Significant non-additive or epistatic effects were observed when stabilizing mutations from different regions of the barrel were combined. The molecular basis of epistasis in DeNovoTIMs appears to be related to the extension of the hydrophobic cores. This study is an important step towards the fine-tuned modulation of protein stability by design.

PubMed: 34271011
DOI: 10.1016/j.jmb.2021.167153

実験手法

X-RAY DIFFRACTION (1.638 Å)