Evidence map›Paper›PMID 33265897›Full record

ReviewAntibiotics (Basel, Switzerland)2020

Design, Screening, and Testing of Non-Rational Peptide Libraries with Antimicrobial Activity: In Silico and Experimental Approaches.

Paola Ruiz Puentes, María C Henao, Carlos E Torres, Saúl C Gómez, Laura A Gómez, Juan C Burgos, Pablo Arbeláez, Johann F Osma, Carolina Muñoz-Camargo, Luis H Reyes and 1 more

Abstract readReview
In one paragraph

Review in Antibiotics (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 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

11 authors.

Paola Ruiz PuentesCenter for Research and Formation in Artificial Intelligence, Universidad de los Andes, Bogota DC 111711, Colombia.ORCID 0000-0003-4352-7999
María C HenaoGrupo de Diseño de Productos y Procesos, Department of Chemical and Food Engineering, Universidad de los Andes, Bogota DC 111711, Colombia.
Carlos E TorresDepartment of Biomedical Engineering, Universidad de los Andes, Bogota DC 111711, Colombia.ORCID 0000-0001-7196-7997
Saúl C GómezDepartment of Biomedical Engineering, Universidad de los Andes, Bogota DC 111711, Colombia.ORCID 0000-0002-3459-3225
Laura A GómezDepartment of Biomedical Engineering, Universidad de los Andes, Bogota DC 111711, Colombia.
Juan C BurgosChemical Engineering Program, Universidad de Cartagena, Cartagena 130015, Colombia.
Pablo ArbeláezCenter for Research and Formation in Artificial Intelligence, Universidad de los Andes, Bogota DC 111711, Colombia.ORCID 0000-0001-5244-2407
Johann F OsmaDepartment of Electrical and Electronic Engineering, Universidad de los Andes, Bogota DC 111711, Colombia.ORCID 0000-0003-2928-3406
Carolina Muñoz-CamargoDepartment of Biomedical Engineering, Universidad de los Andes, Bogota DC 111711, Colombia.ORCID 0000-0001-6238-9021
Luis H ReyesGrupo de Diseño de Productos y Procesos, Department of Chemical and Food Engineering, Universidad de los Andes, Bogota DC 111711, Colombia.ORCID 0000-0001-7251-5298
Juan C CruzDepartment of Biomedical Engineering, Universidad de los Andes, Bogota DC 111711, Colombia.ORCID 0000-0002-7790-7546

Funding

Minciencias 120380763212 - PPTA # 8352Minciencias 689-2018
6 · The paper itself

Abstract

One of the challenges of modern biotechnology is to find new routes to mitigate the resistance to conventional antibiotics. Antimicrobial peptides (AMPs) are an alternative type of biomolecules, naturally present in a wide variety of organisms, with the capacity to overcome the current microorganism resistance threat. Here, we reviewed our recent efforts to develop a new library of non-rationally produced AMPs that relies on bacterial genome inherent diversity and compared it with rationally designed libraries. Our approach is based on a four-stage workflow process that incorporates the interplay of recent developments in four major emerging technologies: artificial intelligence, molecular dynamics, surface-display in microorganisms, and microfluidics. Implementing this framework is challenging because to obtain reliable results, the in silico algorithms to search for candidate AMPs need to overcome issues of the state-of-the-art approaches that limit the possibilities for multi-space data distribution analyses in extremely large databases. We expect to tackle this challenge by using a recently developed classification algorithm based on deep learning models that rely on convolutional layers and gated recurrent units. This will be complemented by carefully tailored molecular dynamics simulations to elucidate specific interactions with lipid bilayers. Candidate AMPs will be recombinantly-expressed on the surface of microorganisms for further screening via different droplet-based microfluidic-based strategies to identify AMPs with the desired lytic abilities. We believe that the proposed approach opens opportunities for searching and screening bioactive peptides for other applications.

Indexed as

antibiotic resistanceantimicrobial peptidesdeep learninglibrary screeningmicrofluidicsmolecular dynamicsnon-rationalrational

Identifiers

PMID33265897
PMCPMC7759991

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.