Evidence map›Paper›PMID 40549759›Full record

ArticlePloS one2025

Estimating the relative rates of lipopolysaccharide synthesis in Escherichia coli K-12 by click chemistry-mediated labeling.

Sheng Shu, Wei Mi

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

2 authors.

Sheng ShuDepartment of Pharmacology, Yale University School of Medicine, New Haven, Connecticut, United States of America.ORCID 0000-0002-1604-4732
Wei MiDepartment of Pharmacology, Yale University School of Medicine, New Haven, Connecticut, United States of America.ORCID 0000-0002-2845-4608

Funding

Understanding how membrane composition directs membrane protein structure and functionRM1GM149406 · NIGMS · YALE UNIVERSITY · PI Joel Adam Butterwick, KATHRYN M FERGUSON · 2023 to 2026
$8.4M
NIGMS NIH HHS RM1 GM149406
6 · The paper itself

Abstract

Lipopolysaccharide (LPS), a critical glycolipid component of Gram-negative bacteria, plays a central role in bacterial membrane integrity and host immune interactions. Despite extensive studies on the regulation of LPS synthesis, methods to quantify its synthesis rate remain limited. Here, we present a novel approach to measure in vivo LPS synthesis rates in the E. coli K-12 strain MG1655 using click chemistry. This method involves the incorporation of an exogenous Kdo analog, 8-azido-3,8-dideoxy-D-manno-oct-2-ulosonic acid (Kdo-N3), into newly synthesized LPS, followed by a copper-free click reaction with a fluorescent alkyne. The labeled LPS is separated by SDS-PAGE and visualized via in-gel fluorescence. We compared two fluorescent dyes and found that AZDye 488 DBCO exhibited stronger sensitivity for labeling LPS during the log phase of bacterial growth. Our results further demonstrated that the amount of newly synthesized LPS correlates linearly with the pulse labeling time of Kdo-N3, validating this approach as a reliable method for estimating relative LPS synthesis rates during the exponential phase of E. coli MG1655 growth. This method offers a reliable, non-radioactive approach for measuring LPS synthesis in vivo, providing a powerful tool to investigate bacterial physiology and the regulation of LPS biogenesis.

Indexed as

Click ChemistryEscherichia coli K12LipopolysaccharidesAzidesFluorescent DyesStaining and LabelingAzidesFluorescent DyesLipopolysaccharides

Identifiers

PMID40549759
PMCPMC12184891

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.