Evidence map›Paper›PMID 42244599›Full record

ArticlebioRxiv : the preprint server for biology2026

SynFit: Synergistic Contrastive Learning for Multi-Objective Protein Fitness Prediction and Optimization.

Tony Tu, Wei Huang, Ziang Li, Kerr Ding, Yang Yang, Yunan Luo

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

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

6 authors.

Tony TuSchool of Computational Science and Engineering, Georgia Institute of Technology.
Wei HuangDepartment of Chemistry and Biochemistry, University of California, Santa Barbara.ORCID 0009-0000-9476-8931
Ziang LiSchool of Computational Science and Engineering, Georgia Institute of Technology.
Kerr DingSchool of Computational Science and Engineering, Georgia Institute of Technology.
Yang YangDepartment of Chemistry and Biochemistry, University of California, Santa Barbara.
Yunan LuoSchool of Computational Science and Engineering, Georgia Institute of Technology.ORCID 0000-0001-7728-6412

Funding

An Evolvable Metalloenzyme Platform for Stereoselective Radical BiocatalysisR35GM147387 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI Yang Yang · 2022 to 2026
$2.0M
Integrative deep learning algorithms for understanding protein sequence-structure-function relationships: representation, prediction, and discoveryR35GM150890 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI Yunan Luo · 2023 to 2026
$1.6M
NIGMS NIH HHS R35 GM147387NIGMS NIH HHS R35 GM150890
6 · The paper itself

Abstract

Proteins function through a complex interplay of structural and biochemical properties, and mutations can reshape these properties to generate fitness landscapes spanning multiple functional objectives. A central challenge in protein engineering is the need to simultaneously optimize multiple properties. In biocatalysis, for example, practical enzyme development routinely requires the concurrent optimization of catalytic activity, selectivity, stability, and substrate generality. However, despite recent advances in computational protein design and fitness prediction, most existing approaches treat these properties independently and do not explicitly capture the dependencies and trade-offs that govern real-world protein performance. We present SynFit, a multi-objective learning framework that integrates pretrained protein language models with experimental fitness measurements for protein fitness prediction and engineering. SynFit learns both shared and property-specific protein sequence representations through a synergistic contrastive learning strategy, enabling the identification of variants that simultaneously optimize multiple functional properties. Across a large-scale multi-fitness deep mutational scanning benchmark, SynFit consistently outperforms state-of-the-art supervised models trained on individual objectives and more accurately identifies variants that balance competing functional constraints. We further applied SynFit to multi-objective enzyme design for a new-to-nature biocatalytic enantioselective borylation reaction, providing a diverse array of novel cytochrome

Identifiers

PMID42244599
PMCPMC13232210

What Socratic 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 Socratic graph.