De novo design of porphyrin-containing proteins as efficient and stereoselective catalysts

De novo design of protein catalysts with high efficiency and stereoselectivity provides an attractive approach toward the design of environmentally benign catalysts. Here, we design proteins that incorporate histidine-ligated synthetic porphyrin and heme ligands. Four of 10 designed proteins catalyzed cyclopropanation with an enantiomeric ratio greater than 99:1. A second class of proteins were designed to catalyze a silicon-hydrogen insertion and were optimized by directed evolution in whole cells. The evolved proteins incorporated features unlikely to be generated by computational design alone, including a proline in an α helix. Molecular dynamics simulations showed that as the proteins evolved toward higher activity, their conformational ensembles narrowed to favor more productive conformations. Our work demonstrates that efficient de novo protein catalysts are designable and should be useful for manifold chemical processes.

Authors

Institutions

Publication Details

Journal
Science
Published
2025-05-08
DOI
https://doi.org/10.1126/science.adt7268
Citations
31
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
29.02
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

De novo design of porphyrin-containing proteins as efficient and stereoselective catalysts

Turki M. Alturaifi, William F. DeGrado, Peng Liu, Thomas H. Tugwell et al.
31 citations
Science
Cyclopropane Reaction Mechanisms
29.02
article

De novo design of porphyrin-containing proteins as efficient and stereoselective catalysts

Turki M. Alturaifi, William F. DeGrado, Peng Liu, Thomas H. Tugwell, Samuel I. Mann, Xingjie Zhang, Kai-Peng Hou, Lei Lü, Yang Yang, Miao Qi, Yuda Chen, Wei Huang
article en
31 citations

Abstract

De novo design of protein catalysts with high efficiency and stereoselectivity provides an attractive approach toward the design of environmentally benign catalysts. Here, we design proteins that incorporate histidine-ligated synthetic porphyrin and heme ligands. Four of 10 designed proteins catalyzed cyclopropanation with an enantiomeric ratio greater than 99:1. A second class of proteins were designed to catalyze a silicon-hydrogen insertion and were optimized by directed evolution in whole cells. The evolved proteins incorporated features unlikely to be generated by computational design alone, including a proline in an α helix. Molecular dynamics simulations showed that as the proteins evolved toward higher activity, their conformational ensembles narrowed to favor more productive conformations. Our work demonstrates that efficient de novo protein catalysts are designable and should be useful for manifold chemical processes.

ScienceVol. 388(6747)
University of California, Riverside (US), University of California, Santa Barbara (US), University of Pittsburgh (US), University of California, San Francisco (US)
Responsible consumption and production
Openalex Percentile: Top 0%
Cyclopropane Reaction Mechanisms
29.02
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.