Evidence map›Paper›PMID 35562950›Full record

ReviewInternational journal of molecular sciences2022

Atomic-Resolution Structures and Mode of Action of Clinically Relevant Antimicrobial Peptides.

Surajit Bhattacharjya, Sk Abdul Mohid, Anirban Bhunia

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
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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

3 authors.

Surajit BhattacharjyaSchool of Biological Sciences, 60 Nanyang Drive, Nanyang Technological University, Singapore 637551, Singapore.ORCID 0000-0001-7015-1937
Sk Abdul MohidDepartment of Biophysics, Bose Institute, Unified Academic Campus, Saltlake, Sector V, EN 80, Kolkata 700091, India.ORCID 0000-0002-6574-0179
Anirban BhuniaDepartment of Biophysics, Bose Institute, Unified Academic Campus, Saltlake, Sector V, EN 80, Kolkata 700091, India.ORCID 0000-0002-8752-2842

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Global rise of infections and deaths caused by drug-resistant bacterial pathogens are among the unmet medical needs. In an age of drying pipeline of novel antibiotics to treat bacterial infections, antimicrobial peptides (AMPs) are proven to be valid therapeutics modalities. Direct in vivo applications of many AMPs could be challenging; however, works are demonstrating encouraging results for some of them. In this review article, we discussed 3-D structures of potent AMPs e.g., polymyxin, thanatin, MSI, protegrin, OMPTA in complex with bacterial targets and their mode of actions. Studies on human peptide LL37 and de novo-designed peptides are also discussed. We have focused on AMPs which are effective against drug-resistant Gram-negative bacteria. Since treatment options for the infections caused by super bugs of Gram-negative bacteria are now extremely limited. We also summarize some of the pertinent challenges in the field of clinical trials of AMPs.

Indexed as

Antimicrobial PeptidesGram-Negative BacteriaAnti-Bacterial AgentsBacteriaHumansAnti-Bacterial AgentsAntimicrobial Peptidesantibioticsantimicrobial peptides (AMPs)lipopolysaccharide (LPS)MDR Gram negative bacteriamechanism of AMPsmultidrug resistant (MDR) bacteria

Identifiers

PMID35562950
PMCPMC9100274

What OpenQuestion holds

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LicenceCC BY
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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.