Evidence map›Paper›PMID 40160427›Full record

ArticleiScience2025

Pareto-optimal sampling for multi-objective protein sequence design.

Jiaqi Luo, Kerr Ding, Yunan Luo

Abstract read
In one paragraph

Article in iScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. AI-Driven De Novo Binder Design: From Structure Prediction to Closed-Loop Optimization.Computational and structural biotechnology journal · 2026
    Review
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

3 authors.

Jiaqi LuoSchool of Computational Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30308, USA.
Kerr DingSchool of Computational Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30308, USA.
Yunan LuoSchool of Computational Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30308, USA.

Funding

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 GM150890
6 · The paper itself

Abstract

Supervised machine learning (ML) has significantly advanced sequence-based protein property prediction. However, its inverse application, designing protein sequences with desired properties, remains under-explored. The challenges in sequence design stem from the vast search space and the rugged protein fitness landscape. In this work, we present MosPro, an efficient ML algorithm for property-guided protein sequence design. We frame sequence design as a discrete sampling problem. Utilizing a pre-trained differentiable ML model that predicts properties of sequences, MosPro shapes a distribution that assigns high probability mass to regions for high-property sequences. To generate designs, MosPro efficiently samples sequences from this constructed distribution. We further develop a Pareto optimization algorithm to propose sequences that are simultaneously optimized for multiple properties. Evaluations on experimental fitness landscapes demonstrated that MosPro generates sequences that optimally trade off multiple desiderata. Our results suggested an unparalleled potential of generative ML for efficient and controllable design for functional proteins.

Indexed as

Behavioral neuroscienceCognitive neuroscienceNeuroscience

Identifiers

PMID40160427
PMCPMC11952807

What OpenQuestion holds

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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.