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1.
PLoS Comput Biol ; 20(5): e1012063, 2024 May.
Artigo em Inglês | MEDLINE | ID: mdl-38743804

RESUMO

In this work, we quantitatively compare computer simulations and existing cell tracking data of P. aeruginosa surface motility in order to analyse the underlying motility mechanism. We present a three dimensional twitching motility model, that simulates the extension, retraction and surface association of individual Type IV Pili (TFP), and is informed by recent experimental observations of TFP. Sensitivity analysis is implemented to minimise the number of model parameters, and quantitative estimates for the remaining parameters are inferred from tracking data by approximate Bayesian computation. We argue that the motility mechanism is highly sensitive to experimental conditions. We predict a TFP retraction speed for the tracking data we study that is in a good agreement with experimental results obtained under very similar conditions. Furthermore, we examine whether estimates for biologically important parameters, whose direct experimental determination is challenging, can be inferred directly from tracking data. One example is the width of the distribution of TFP on the bacteria body. We predict that the TFP are broadly distributed over the bacteria pole in both walking and crawling motility types. Moreover, we identified specific configurations of TFP that lead to transitions between walking and crawling states.


Assuntos
Biologia Computacional , Simulação por Computador , Fímbrias Bacterianas , Modelos Biológicos , Pseudomonas aeruginosa , Pseudomonas aeruginosa/fisiologia , Fímbrias Bacterianas/fisiologia , Teorema de Bayes , Movimento/fisiologia
2.
Bioinformatics ; 34(11): 1939-1940, 2018 06 01.
Artigo em Inglês | MEDLINE | ID: mdl-29390042

RESUMO

Summary: JABAWS 2.2 is a computational framework that simplifies the deployment of web services for Bioinformatics. In addition to the five multiple sequence alignment (MSA) algorithms in JABAWS 1.0, JABAWS 2.2 includes three additional MSA programs (Clustal Omega, MSAprobs, GLprobs), four protein disorder prediction methods (DisEMBL, IUPred, Ronn, GlobPlot), 18 measures of protein conservation as implemented in AACon, and RNA secondary structure prediction by the RNAalifold program. JABAWS 2.2 can be deployed on a variety of in-house or hosted systems. JABAWS 2.2 web services may be accessed from the Jalview multiple sequence analysis workbench (Version 2.8 and later), as well as directly via the JABAWS command line interface (CLI) client. JABAWS 2.2 can be deployed on a local virtual server as a Virtual Appliance (VA) or simply as a Web Application Archive (WAR) for private use. Improvements in JABAWS 2.2 also include simplified installation and a range of utility tools for usage statistics collection, and web services querying and monitoring. The JABAWS CLI client has been updated to support all the new services and allow integration of JABAWS 2.2 services into conventional scripts. A public JABAWS 2 server has been in production since December 2011 and served over 800 000 analyses for users worldwide. Availability and implementation: JABAWS 2.2 is made freely available under the Apache 2 license and can be obtained from: http://www.compbio.dundee.ac.uk/jabaws. Contact: g.j.barton@dundee.ac.uk.


Assuntos
Biologia Computacional/métodos , Conformação de Ácido Nucleico , RNA/metabolismo , Software , Algoritmos , Internet , Modelos Moleculares , Deficiências na Proteostase , RNA/química , Alinhamento de Sequência , Análise de Sequência de Proteína/métodos , Análise de Sequência de RNA/métodos
3.
PLoS Comput Biol ; 13(6): e1005569, 2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-28665934

RESUMO

We introduce an Active Vertex Model (AVM) for cell-resolution studies of the mechanics of confluent epithelial tissues consisting of tens of thousands of cells, with a level of detail inaccessible to similar methods. The AVM combines the Vertex Model for confluent epithelial tissues with active matter dynamics. This introduces a natural description of the cell motion and accounts for motion patterns observed on multiple scales. Furthermore, cell contacts are generated dynamically from positions of cell centres. This not only enables efficient numerical implementation, but provides a natural description of the T1 transition events responsible for local tissue rearrangements. The AVM also includes cell alignment, cell-specific mechanical properties, cell growth, division and apoptosis. In addition, the AVM introduces a flexible, dynamically changing boundary of the epithelial sheet allowing for studies of phenomena such as the fingering instability or wound healing. We illustrate these capabilities with a number of case studies.


Assuntos
Comunicação Celular/fisiologia , Células Epiteliais/citologia , Células Epiteliais/fisiologia , Epitélio/fisiologia , Mecanotransdução Celular/fisiologia , Modelos Biológicos , Animais , Apoptose/fisiologia , Movimento Celular/fisiologia , Proliferação de Células/fisiologia , Simulação por Computador , Módulo de Elasticidade/fisiologia , Humanos , Mitose/fisiologia , Morfogênese/fisiologia , Tamanho do Órgão/fisiologia , Estresse Mecânico , Cicatrização/fisiologia
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