Evidence map›Paper›PMID 42869909›Full record

ArticleNature communications2026

Functional alignment of protein language models via reinforcement learning.

Nathaniel Blalock, Srinath Seshadri, Kensuke Nakamura, Agrim Babbar, Sarah A Fahlberg, Ameya Kulkarni, Philip A Romero

Abstract read
In one paragraph

Article in Nature communications, 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

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Nathaniel BlalockDepartment of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0000-0001-7993-7936
Srinath SeshadriDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Kensuke NakamuraDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Agrim BabbarDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI, USA.
Sarah A FahlbergDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI, USA.
Ameya KulkarniDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Philip A RomeroDepartment of Biomedical Engineering, Duke University, Durham, NC, USA. philip.romero@duke.edu.ORCID 0000-0002-2586-7263

Funding

Self-driving laboratories for autonomous exploration of protein sequence spaceR01GM150929 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Philip Anthony Romero · 2023 to 2026
$1.4M
NIGMS NIH HHS R01 GM150929
6 · The paper itself

Abstract

Protein language models (pLMs) enable generative design of novel protein sequences but remain fundamentally misaligned with protein engineering goals, as they lack explicit understanding of function and often fail to improve properties beyond those found in nature. We introduce Reinforcement Learning from eXperimental Feedback (RLXF), a general framework that aligns protein language models with experimentally measured functional objectives, drawing inspiration from the methods used to align large language models like ChatGPT. Applied across five diverse protein families, RLXF improves generation of high-functioning variants beyond pre-trained baselines. We demonstrate this with CreiLOV, an oxygen-independent fluorescent protein, where RLXF-aligned models generate sequences with significantly enhanced fluorescence, including the most fluorescent CreiLOV variants reported to date. Our results indicate that RLXF-aligned models effectively integrate the evolutionary knowledge encoded in pre-trained pLMs with experimental observations, improving the success rate of generated sequences and enabling the discovery of synergistic mutation combinations that are difficult to identify through zero-shot or evolutionary approaches. RLXF provides a scalable and accessible approach to steer generative models toward desired biochemical properties, enabling function-driven protein design beyond the limits of natural evolution.

Indexed as

Protein EngineeringProteinsGenerative Artificial IntelligenceLarge Language ModelsReinforcement Machine LearningProteins

Identifiers

PMID42869909
PMCPMC13662182

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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.