Evidence map›Paper›PMID 39075114›Full record

ArticleScientific reports2024

Ionic liquid-assisted sample preparation mediates sensitive proteomic analysis of Bacillus subtilis spores.

Masato Taoka, Ritsuko Kuwana, Tatsumi Fukube, Akiko Kashima, Yuko Nobe, Takamasa Uekita, Tohru Ichimura, Hiromu Takamatsu

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

8 authors.

Masato Taoka *Department of Chemistry, Tokyo Metropolitan University, Tokyo, 192-0397, Japan. mango@tmu.ac.jp.
Ritsuko Kuwana *Faculty of Pharmaceutical Science, Setsunan University, Osaka, 573-0101, Japan.
Tatsumi FukubeDepartment of Applied Chemistry, National Defense Academy, Yokosuka, Kanagawa, 239-8686, Japan.
Akiko KashimaCarriere Reseau Co., Ltd., Kanagawa, 238-0011, Japan.
Yuko NobeDepartment of Chemistry, Tokyo Metropolitan University, Tokyo, 192-0397, Japan.
Takamasa UekitaDepartment of Applied Chemistry, National Defense Academy, Yokosuka, Kanagawa, 239-8686, Japan.
Tohru IchimuraDepartment of Applied Chemistry, National Defense Academy, Yokosuka, Kanagawa, 239-8686, Japan. ichimura@nda.ac.jp.
Hiromu TakamatsuFaculty of Pharmaceutical Science, Setsunan University, Osaka, 573-0101, Japan.

Funding

Ministry of Education, Culture, Sports, Science and Technology of Japan through Grants-in-Aid for Scientific Research 21K05322
6 · The paper itself

Abstract

Endospore-forming bacteria are ubiquitous. Bacterial endospores are multilayered proteinaceous structures that protects the bacterial genome during stress conditions. They are also responsible for a wide range of critical clinical infections in humans. Precise analysis of spore-forming pathogens remains a major challenge in the field of proteomics because spore structures are highly resistant to conventional solubilizers and denaturing agents, such as sodium dodecyl sulfate and urea. We present an ionic liquid-assisted (i-soln) technique of sample preparation, called pTRUST, which enables shotgun analysis of Bacillus subtilis spores even when the starting materials are in the sub-microgram range. In proteomic analysis, this technique shows 50-2000-fold higher sensitivity than other conventional gel-based or gel-free methods (including one-pot sample processing). Using this technique, we identified 445 proteins with high confidence from trace amounts of highly pure spore preparations, including 52 of the 79 proteins (approximately 70%) previously demonstrated to be localized in spores in the SubtiWiki database and detected through direct protein analysis. Consequently, 393 additional proteins were identified as candidates for spore constitutive proteins. Twenty of these newly identified candidates were produced as green fluorescent protein fusion proteins, and each was evaluated for authenticity as a spore constituent using fluorescence microscopy analysis. The pTRUST method's sensitivity and reliability using the i-soln system, together with hitherto unreported proteins in spores, will enable an array of spore research for biological and clinical applications.

Indexed as

Bacillus subtilisBacterial ProteinsIonic LiquidsProteomicsSpores, BacterialProteomeBacterial ProteinsIonic LiquidsProteomeBacillus subtilisEndosporeIonic liquidProteomicspTRUST

Identifiers

PMID39075114
PMCPMC11286849

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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.