8AF2

Human Sterol Carrier Protein with unnatural amino acid 2,2'-bipyridine alanine incorporated at position 111

8AF2 の概要

• エントリーDOI: 10.2210/pdb8af2/pdb
• 分子名称: Enoyl-CoA hydratase 2, FRAGMENT OF TRITON X-100, SULFATE ION, ... (5 entities in total)
• 機能のキーワード: de novo protein, artificial metalloenzyme incorporating unnatural amino acid 2, 2-bipyridine, copper ion bound, metal binding protein
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 29977.87

構造登録者

Richardson, J.M.,Klemencic, E.,Jarvis, A.G. (登録日: 2022-07-15, 公開日: 2023-08-16, 最終更新日: 2024-04-03)

主引用文献

Klemencic, E.,Brewster, R.C.,Ali, H.S.,Richardson, J.M.,Jarvis, A.G.
Using BpyAla to generate copper artificial metalloenzymes: a catalytic and structural study.
Catalysis Science And Technology, 14:1622-1632, 2024

PubMed Abstract: Artificial metalloenzymes (ArMs) have emerged as a promising avenue in the field of biocatalysis, offering new reactivity. However, their design remains challenging due to the limited understanding of their protein dynamics and how the introduced cofactors alter the protein scaffold structure. Here we present the structures and catalytic activity of novel copper ArMs capable of ()- or ()-stereoselective control, utilizing a steroid carrier protein (SCP) scaffold. To incorporate 2,2'-bipyridine (Bpy) into SCP, two distinct strategies were employed: either Bpy was introduced as an unnatural amino acid (2,2'-bipyridin-5-yl)alanine (BpyAla) using amber stop codon expression or bioconjugation of bromomethyl-Bpy to cysteine residues. The resulting ArMs proved to be effective at catalysing an enantioselective Friedel-Crafts reaction with SCP_Q111BpyAla achieving the best selectivity with an enantioselectivity of 72% (). Interestingly, despite using the same protein scaffold, different attachment strategies for Bpy at the same residue (Q111) led to a switch in the enantiopreference of the ArM. X-ray crystal structures of SCP_Q111CBpy and SCP_Q111BpyAla ArMs with bound Cu(ii) ions unveiled crucial differences in the orientation of the catalytic centre. Combining structural information, alanine scanning studies, and computational analysis shed light on the distinct active sites of the ArMs, clarifying that these active sites stabilise the nucleophilic substrate on different sides of the electrophile leading to the observed switch in enantioselectivity. This work underscores the importance of integrating structural studies with catalytic screening to unravel the intricacies of ArM behaviour and facilitate their development for targeted applications in biocatalysis.

PubMed: 38505507
DOI: 10.1039/d3cy01648j

実験手法

X-RAY DIFFRACTION (2.51 Å)