Evidence map›Paper›PMID 29246750›Full record

ArticleAnalytical biochemistry2018

False positives in using the zymogram assay for identification of peptidoglycan hydrolases.

Cristian A Escobar, Timothy A Cross

Abstract read
In one paragraph

Article in Analytical biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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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

7 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

2 authors.

Cristian A EscobarInstitute of Molecular Biophysics, and National High Magnetic Field Laboratory, Florida State University, Tallahassee, FL 32310 USA.
Timothy A CrossDepartment of Chemistry and Biochemistry, Institute of Molecular Biophysics, and National High Magnetic Field Laboratory, Florida State University, Tallahassee, FL 32310 USA. Electronic address: cross@magnet.fsu.edu.

Funding

Membrane Protein Structures and Interactions in the M. tuberculosis DivisomeR01AI119178 · NIAID · FLORIDA STATE UNIVERSITY · PI CROSS, TIMOTHY A · 2015 to 2019
$3.6M
NIAID NIH HHS R01 AI119178
6 · The paper itself

Abstract

Zymogram assays have been used extensively to identify novel peptidoglycan hydrolases. In this study it is reported that the zymogram is susceptible to false positive results when highly positively charged proteins are assayed. As an example, we report on the case of the ChiZ membrane protein from the Mycobacterium tuberculosis divisome, which previously was described as a peptidoglycan hydrolase. Even though the full length ChiZ protein was able to produce positive assay results, other direct methods for measuring peptidoglycan hydrolysis do not provide convincing evidence that ChiZ has peptidoglycan hydrolysis activity. We show that the false positive result is produced by the highly positively charged N-terminal region of ChiZ. Thus, we developed a zymogram control that can be used to identify false positives results. This control assay lacks the refolding step in the normal zymogram assay. For lysozyme the control assay shows no activity, while the N-terminal region of ChiZ shows a false positive result. Given the limitations of the zymogram assay to reliably identify peptidoglycan hydrolases, we recommend using the zymogram control assay together with other methods to evaluate possible peptidoglycan hydrolysis activity.

Indexed as

Electrophoresis, Polyacrylamide GelBacterial ProteinsCytoskeletal ProteinsFalse Positive ReactionsHumansMycobacterium tuberculosisN-Acetylmuramoyl-L-alanine AmidaseBacterial ProteinsCytoskeletal ProteinsFtsZ protein, BacteriaN-Acetylmuramoyl-L-alanine AmidaseChiZLysozymePeptidoglycan hydrolysisZymogram assay

Identifiers

PMID29246750
PMCPMC5826805

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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.