Evidence map›Paper›PMID 41676228›Full record

ArticleACS catalysis2026

Advancing NanoLuc Luciferase Stability beyond Directed Evolution and Rational Design through Expert-Guided Deep Learning.

Spencer Gardiner, Joseph Talley, Tyler Green, Christopher Haynie, Corbyn Kubalek, Matthew Argyle, William Heaps, Joshua Ebbert, Deon Allen, Dallin Chipman and 2 more

Abstract read
In one paragraph

Article in ACS catalysis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Spencer GardinerDepartment of Physics and Astronomy, Brigham Young University, Provo, Utah 84602, United States.
Joseph TalleyDepartment of Chemical Engineering, Brigham Young University, Provo, Utah 84602, United States.
Tyler GreenDepartment of Chemical Engineering, Brigham Young University, Provo, Utah 84602, United States.
Christopher HaynieDepartment of Physics and Astronomy, Brigham Young University, Provo, Utah 84602, United States.
Corbyn KubalekDepartment of Physics and Astronomy, Brigham Young University, Provo, Utah 84602, United States.
Matthew ArgyleDepartment of Physics and Astronomy, Brigham Young University, Provo, Utah 84602, United States.
William HeapsDepartment of Physics and Astronomy, Brigham Young University, Provo, Utah 84602, United States.
Joshua EbbertDepartment of Physics and Astronomy, Brigham Young University, Provo, Utah 84602, United States.
Deon AllenDepartment of Physics and Astronomy, Brigham Young University, Provo, Utah 84602, United States.
Dallin ChipmanDepartment of Chemical Engineering, Brigham Young University, Provo, Utah 84602, United States.
Bradley C BundyDepartment of Chemical Engineering, Brigham Young University, Provo, Utah 84602, United States.ORCID https://orcid.org/0000-0003-4438-183X
Dennis Della CorteDepartment of Physics and Astronomy, Brigham Young University, Provo, Utah 84602, United States.ORCID https://orcid.org/0000-0002-8884-9724

Funding

Engineering Enzymes for Improved Stability and Retained Function via Rapid Design-Build-Test-Learn Cycles integrating AI/Physics based predictions with Cell-free Protein Synthesis Experimental TestingR15GM155803 · NIGMS · BRIGHAM YOUNG UNIVERSITY · PI DELLA CORTE, DENNIS · 2024 to 2024
$449k
NIGMS NIH HHS R15 GM155803
6 · The paper itself

Abstract

Engineered luciferases have transformed biological imaging and sensing, yet optimizing NanoLuc luciferase (NLuc) remains challenging due to the inherent stability-activity trade-off and its limited sequence homology with characterized proteins. We report a hybrid approach that synergistically integrates deep learning with structure-guided rational design to develop enhanced NLuc variants that improve thermostability and thereby activity at elevated temperatures. By systematically analyzing libraries of engineered variants, we established that modifications to termini and loops distal from the catalytic center, combined with preservation of allosterically coupled networks, effectively increase thermal resilience while maintaining enzymatic function. Our optimized variantsnotably B.07 and B.09exhibit substantial thermostability enhancements (increased melting temperatures of 7.2 and 5.1 °C, respectively), leading to the sustained activity of a high-activity mutant at elevated temperatures. Molecular dynamics simulations and protein folding studies elucidate how these mutations favorably modulate conformational landscapes without perturbing the substrate binding architecture. Beyond providing a thermostabilized tool for bioluminescence applications, our integrated methodology presents a framework for engineering enzymes when traditional homology-based approaches fail and stability-activity constraints present formidable barriers to improvement.

Indexed as

cell-free protein synthesisdeep learningenzyme engineeringinverse protein foldingluciferaserational designthermostability

Identifiers

PMID41676228
PMCPMC12887937

What OpenQuestion holds

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Registered trials

None linked

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.