Evidence map›Paper›PMID 41396131›Full record

ArticleACS chemical biology2026

Continuous Hypermutation and Evolution of Luciferase Variants.

Tanya Hadjian, Ria A Deshpande, Zachary R Torrey, Amelia W Hammond, Rosana S Molina, Kevin Ng, Chang C Liu, Jennifer A Prescher

Abstract read
In one paragraph

Article in ACS chemical biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Tanya HadjianDepartment of Chemistry, University of California, Irvine, California 92697, United States.ORCID 0000-0001-8194-4043
Ria A DeshpandeProgram in Mathematical Computational and Systems Biology, University of California, Irvine, California 92697, United States.
Zachary R TorreyDepartment of Chemistry, University of California, Irvine, California 92697, United States.ORCID 0000-0002-6854-3875
Amelia W HammondDepartment of Chemistry, University of California, Irvine, California 92697, United States.
Rosana S MolinaDepartment of Biomedical Engineering, University of California, Irvine, California 92697, United States.ORCID 0000-0001-7891-2462
Kevin NgDepartment of Pharmaceutical Sciences, University of California, Irvine, California 92697, United States.
Chang C LiuDepartment of Chemistry, University of California, Irvine, California 92697, United States.ORCID 0000-0002-3290-2880
Jennifer A PrescherDepartment of Chemistry, University of California, Irvine, California 92697, United States.ORCID 0000-0002-9250-4702

Funding

Synthetic genetic systems for rapid biomolecular evolution in vivoR35GM136297 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI LIU, CHANG C · 2020 to 2024
$2.4M
NIGMS NIH HHS R35 GM136297
6 · The paper itself

Abstract

Several luciferases have been developed for imaging and biosensing, and the collection continues to grow as new applications are pursued. The current workflow for luciferase optimization, while successful, remains laborious and inefficient. Mutant libraries are generated in vitro and screened, "winning" mutants are picked by hand, and the isolated sequences are subjected to additional rounds of mutagenesis and screening. Here, we present a streamlined platform for luciferase engineering that removes the need for manual library generation during each cycle. We purposed an orthogonal DNA replication (OrthoRep) system for continuous hypermutation of a well-known luciferase (GeNL). Short cycles of culturing and screening were sufficient to evolve the enzyme, with no repetitive manual library generation necessary. New GeNL variants were identified that exhibit improved light outputs with a noncognate and inexpensive luciferin. We further characterized the novel luciferases in cell models. Collectively this work establishes OrthoRep and continuous hypermutation as a viable method to engineer luciferases, and sets the stage for more rapid development of bioluminescent reporters.

Indexed as

Directed Molecular EvolutionLuciferasesDNA ReplicationHumansMutagenesisMutationProtein EngineeringLuciferases

Identifiers

PMID41396131
PMCPMC13348083

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.