Evidence map›Paper›PMID 41412115›Full record

ReviewCell systems2025

Engineering mammalian protein secretion: Toward the convergence of high-throughput biology and computational methods.

Jacopo Gabrielli, Nathan E Lewis, Cleo Kontoravdi, Francesca Ceroni

Abstract readReview
In one paragraph

Review in Cell systems, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

4 authors.

Jacopo GabrielliDepartment of Chemical Engineering, Imperial College London, London, UK; Imperial College Centre for Engineering Biology, Imperial College London, London, UK.
Nathan E LewisComplex Carbohydrate Research Center, Center for Molecular Medicine, & Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA, USA; Department of Biotechnology and Biomedicine, Technical University of Denmark, Kongens Lyngby, Denmark.
Cleo KontoravdiDepartment of Chemical Engineering, Imperial College London, London, UK; Imperial College Centre for Engineering Biology, Imperial College London, London, UK; Bezos Centre for Sustainable Protein, London, UK. Electronic address: cleo.kontoravdi98@imperial.ac.uk.
Francesca CeroniDepartment of Chemical Engineering, Imperial College London, London, UK; Imperial College Centre for Engineering Biology, Imperial College London, London, UK; Bezos Centre for Sustainable Protein, London, UK. Electronic address: f.ceroni@imperial.ac.uk.

Funding

Unraveling the mammalian secretory pathway through systems biology and algorithm developmentR35GM119850 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LEWIS, NATHAN ENOCH · 2016 to 2025
$4.3M
NIGMS NIH HHS R35 GM119850
6 · The paper itself

Abstract

Protein secretion in mammalian cells is the active transport of proteins from the cytoplasm to the extracellular space. It plays a fundamental role in mammalian physiology and signaling, as well as biotherapeutics production and cell and gene therapies. The efficacy of protein secretion, however, is impacted by features of the secreted protein itself, and the host-cell machinery that supports each step of the secretion process. High-throughput techniques such as microfluidics, cell display, and cell encapsulation assays for the study and engineering of secreted proteins are transforming biomedical knowledge and our ability to modulate protein secretion. In addition, computational advances, including signal peptide modeling, whole-protein machine learning models, and genome-scale simulations, are opening new pathways for rational design of protein secretion. Here, we highlight recent developments in secretion engineering that are leading to the convergence of high-throughput experimentation and machine learning methods and can help address current challenges in bioproduction and support future efforts in cell and gene therapy while enabling new modalities.

Indexed as

Computational BiologyProtein EngineeringProteinsAnimalsHigh-Throughput Screening AssaysHumansMachine LearningMammalsProtein TransportProteinsbioproductionbiotherapeuticscell encapsulationcomputational protein designhigh throughputmicrofluidicsprotein engineeringprotein secretionsynthetic biologysystems biology

Identifiers

PMID41412115
PMCPMC12721588

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.