Evidence map›Paper›PMID 41676563›Full record

ArticlebioRxiv : the preprint server for biology2026

Efficient, Few-shot Directed Evolution with Energy Rank Alignment.

Sebastian Ibarraran, Shriram Chennakesavalu, Frank Hu, Grant M Rotskoff

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for 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

4 authors.

Sebastian IbarraranDepartment of Chemistry, Stanford University, Stanford CA 94305.ORCID 0000-0002-3207-8094
Shriram ChennakesavaluDepartment of Chemistry, Stanford University, Stanford CA 94305.ORCID 0000-0002-4750-8923
Frank HuDepartment of Chemistry, Stanford University, Stanford CA 94305.ORCID 0009-0001-4783-0947
Grant M RotskoffDepartment of Chemistry, Stanford University, Stanford CA 94305.ORCID 0000-0002-7772-5179

Funding

Generative multiscale models of biomolecular conformational dynamics: from fluctuations to many-component assembliesR35GM159834 · NIGMS · STANFORD UNIVERSITY · PI Grant Rotskoff · 2025 to 2026
$820k
NIGMS NIH HHS R35 GM159834
6 · The paper itself

Abstract

Directed evolution is a powerful and widely used technique for protein engineering, and reducing the cost of iterated experimental observations has become a major priority for practitioners. A number of recent efforts to use machine-learning-based predictors to improve sequence selection have led to remarkable improvements in efficiency, but the sparse data at each experimental iteration restricts these approaches to extremely simple models. Adapting large-scale pre-trained protein language models using experimental data offers an alternative that we show productively leverages the strong inductive biases of the natural distribution of protein sequences to navigate high-dimensional, combinatorially large fitness landscapes. Our approach uses a general-purpose "post-training" algorithm grounded in statistical physics that employs quantitative experimental rankings to directly produce a sampler for diverse, high fitness sequences with fewer data points than competing methods. The resulting adapted protein language model can itself be studied and interpreted, shedding further light on the biophysical characteristics of highly fit sequences and their properties.

Identifiers

PMID41676563
PMCPMC12889597

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.