Continuous targeted hypermutation with a tunable mutation window

Targeted in vivo hypermutation drives rapid sequence diversification within specific DNA regions of living cells, enabling continuous evolution of biomolecules for enhanced functionality. In living organisms, this is prominently illustrated by the preferential somatic hypermutation of complementarity-determining regions during antibody affinity maturation. This particular targeting strategy employs focused mutagenesis in predefined, functionally important intragenic regions and should ideally allow for target range adjustment to support broader applications. However, molecular tools incorporating these features remain limited. Here, we present RESPECTevo, a system for focused hypermutation of endogenous and heterologous regions up to ~200 bp with predefined boundaries. By leveraging specific targeting capability, spacer length flexibility, and mismatch tolerance of the Escherichia coli Cascade complex, RESPECTevo enables highly specific targeted hypermutation, target range modulation, and continuous hypermutation across dual regions. Collectively, RESPECTevo serves as an efficient platform for hypermutating user-defined target regions in living cells, facilitating continuous protein evolution for biotechnological applications.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2025-11-25
DOI
https://doi.org/10.1038/s41467-025-66736-2
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Continuous targeted hypermutation with a tunable mutation window

Seokhee Kim, Chanwoo Lee
Nature Communications
Monoclonal and Polyclonal Antibodies Research
article

Continuous targeted hypermutation with a tunable mutation window

Seokhee Kim, Chanwoo Lee
article en

Abstract

Targeted in vivo hypermutation drives rapid sequence diversification within specific DNA regions of living cells, enabling continuous evolution of biomolecules for enhanced functionality. In living organisms, this is prominently illustrated by the preferential somatic hypermutation of complementarity-determining regions during antibody affinity maturation. This particular targeting strategy employs focused mutagenesis in predefined, functionally important intragenic regions and should ideally allow for target range adjustment to support broader applications. However, molecular tools incorporating these features remain limited. Here, we present RESPECTevo, a system for focused hypermutation of endogenous and heterologous regions up to ~200 bp with predefined boundaries. By leveraging specific targeting capability, spacer length flexibility, and mismatch tolerance of the Escherichia coli Cascade complex, RESPECTevo enables highly specific targeted hypermutation, target range modulation, and continuous hypermutation across dual regions. Collectively, RESPECTevo serves as an efficient platform for hypermutating user-defined target regions in living cells, facilitating continuous protein evolution for biotechnological applications.

Nature CommunicationsVol. 16(1)
Seoul National University (KR), National University College (PR)
Openalex Percentile: Top 49%
Monoclonal and Polyclonal Antibodies Research
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.

Continuous targeted hypermutation with a tunable mutation window — Seokhee Kim, Chanwoo Lee · Nature Communications (2025) | TGRS Research Map | TGRS