Evidence map›Paper›PMID 37328605›Full record

ReviewNature protocols2023

Rapid biosynthesis of glycoprotein therapeutics and vaccines from freeze-dried bacterial cell lysates.

Jessica C Stark, Thapakorn Jaroentomeechai, Katherine F Warfel, Jasmine M Hershewe, Matthew P DeLisa, Michael C Jewett

Open access · greenAbstract readReview
In one paragraph

Review in Nature protocols, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
7.5field-weighted citation impact, top 3% of its field
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

11 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Design of solubly expressed miniaturized SMART MHCs.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Article
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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 at 4 institutions in 2 countries.

Jessica C StarkDepartment of Chemistry & Sarafan ChEM-H, Stanford University, Stanford, CA, USA. jcstark@stanford.edu.ORCID 0000-0003-3828-5438
Thapakorn JaroentomeechaiCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.
Katherine F WarfelDepartment of Chemical and Biological Engineering, Northwestern University, Evanston, IL, USA.ORCID 0000-0002-7780-6294
Jasmine M HersheweDepartment of Chemical and Biological Engineering, Northwestern University, Evanston, IL, USA.
Matthew P DeLisaRobert Frederick Smith School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, NY, USA. md255@cornell.edu.ORCID 0000-0003-3226-1566
Michael C JewettDepartment of Chemical and Biological Engineering, Northwestern University, Evanston, IL, USA. mjewett@stanford.edu.ORCID 0000-0003-2948-6211
Northwestern University · USCornell University · USStanford University · USUniversity of Copenhagen · DK

Funding

Elucidating mechanisms of mucin-mediated immune regulation in cancerF32CA250324 · NCI · STANFORD UNIVERSITY · PI STARK, JESSICA C · 2020 to 2020
$52k
NCI NIH HHS F32 CA250324
6 · The paper itself

Abstract

The advent of distributed biomanufacturing platforms promises to increase agility in biologic production and expand access by reducing reliance on refrigerated supply chains. However, such platforms are not capable of robustly producing glycoproteins, which represent the majority of biologics approved or in development. To address this limitation, we developed cell-free technologies that enable rapid, modular production of glycoprotein therapeutics and vaccines from freeze-dried Escherichia coli cell lysates. Here, we describe a protocol for generation of cell-free lysates and freeze-dried reactions for on-demand synthesis of desired glycoproteins. The protocol includes construction and culture of the bacterial chassis strain, cell-free lysate production, assembly of freeze-dried reactions, cell-free glycoprotein synthesis, and glycoprotein characterization, all of which can be completed in one week or less. We anticipate that cell-free technologies, along with this comprehensive user manual, will help accelerate development and distribution of glycoprotein therapeutics and vaccines.

Indexed as

Escherichia coliVaccinesBacteriaGlycoproteinsProtein BiosynthesisGlycoproteinsVaccines

Identifiers

PMID37328605
PMCPMC13360663
OpenAlexW4380882072

What OpenQuestion holds

Textmetadata
LicenceTDM
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.