Loop‐Centric Engineering of Terminal Deoxynucleotidyl Transferase for Enhanced Catalysis of 3'‐Modified Nucleotides

ABSTRACT Efficient enzymatic DNA synthesis requires terminal deoxynucleotidyl transferases (TdTs) that can accept reversibly blocked nucleotides, but improving wild‐type enzymes has traditionally depended on labor‐intensive screening. Here, we combine deep learning‐based structure prediction with molecular dynamics simulations to guide loop‐centric engineering of a TdT from Crocodylus porosus . The resulting variant M3 (V253E/L256M/N338R) showed a 26‐fold increase in specific activity toward 3'‐ONH 2 ‐dCTP while maintaining expression and thermostability. Simulations indicated that the mutations reorganized Loop1 dynamics and reproducibly biased the incoming nucleotide toward a more favorable in‐line attack orientation. The key N338R change also improved a second TdT scaffold, supporting N338 as a potentially transferable engineering hotspot. These results provide a practical computational strategy for improving terminal deoxynucleotidyl transferases for incorporation of 3′‐modified nucleotides, reducing reliance on large‐scale screening.

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Publication Details

Journal
Biotechnology and Bioengineering
Published
2026-09-30
DOI
https://doi.org/10.1002/bit.70397
Primary Topic
Bacterial Genetics and Biotechnology
Type
article
Field-Weighted Citation Impact
0.00
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article

Loop‐Centric Engineering of Terminal Deoxynucleotidyl Transferase for Enhanced Catalysis of 3'‐Modified Nucleotides

Jian‐He Xu, Ai-Pei Li, Hui‐Lei Yu, Kun Shi
Biotechnology and Bioengineering
Bacterial Genetics and Biotechnology
article

Loop‐Centric Engineering of Terminal Deoxynucleotidyl Transferase for Enhanced Catalysis of 3'‐Modified Nucleotides

Jian‐He Xu, Ai-Pei Li, Hui‐Lei Yu, Kun Shi
article en

Abstract

ABSTRACT Efficient enzymatic DNA synthesis requires terminal deoxynucleotidyl transferases (TdTs) that can accept reversibly blocked nucleotides, but improving wild‐type enzymes has traditionally depended on labor‐intensive screening. Here, we combine deep learning‐based structure prediction with molecular dynamics simulations to guide loop‐centric engineering of a TdT from Crocodylus porosus . The resulting variant M3 (V253E/L256M/N338R) showed a 26‐fold increase in specific activity toward 3'‐ONH 2 ‐dCTP while maintaining expression and thermostability. Simulations indicated that the mutations reorganized Loop1 dynamics and reproducibly biased the incoming nucleotide toward a more favorable in‐line attack orientation. The key N338R change also improved a second TdT scaffold, supporting N338 as a potentially transferable engineering hotspot. These results provide a practical computational strategy for improving terminal deoxynucleotidyl transferases for incorporation of 3′‐modified nucleotides, reducing reliance on large‐scale screening.

Biotechnology and Bioengineering
East China University of Science and Technology (CN)
Openalex Percentile: Top 12%
Bacterial Genetics and Biotechnology
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Loop‐Centric Engineering of Terminal Deoxynucleotidyl Transferase for Enhanced Catalysis of 3'‐Modified Nucleotides — Jian‐He Xu, Ai-Pei Li, et al. · Biotechnology and Bioengineering (2026) | TGRS Research Map | TGRS