Automatic Counting of Intra-Cellular Ribonucleo-Protein Aggregates in Saccharomyces cerevisiae Using a Textural Approach.
Cytoplasm
Cytoplasmic Granules
/ metabolism
Green Fluorescent Proteins
Microscopy, Fluorescence
/ methods
Models, Biological
Poly(A)-Binding Proteins
/ isolation & purification
Protein Aggregates
Ribonucleoproteins
/ isolation & purification
Saccharomyces cerevisiae
/ cytology
Saccharomyces cerevisiae Proteins
/ isolation & purification
Generalized Fourier descriptors
Haralick
Zernike
ribonucleo-protein aggregates
sub-cellular structures
Journal
Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada
ISSN: 1435-8115
Titre abrégé: Microsc Microanal
Pays: England
ID NLM: 9712707
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
pubmed:
14
2
2019
medline:
9
4
2019
entrez:
14
2
2019
Statut:
ppublish
Résumé
In the context of microbiology, recent studies show the importance of ribonucleo-protein aggregates (RNPs) for the understanding of mechanisms involved in cell responses to specific environmental conditions. The assembly and disassembly of aggregates is a dynamic process, the characterization of the stage of their evolution can be performed by the evaluation of their number. The aim of this study is to propose a method to automatically determine the count of RNPs. We show that the determination of a precise count is an issue by itself and hence, we propose three textural approaches: a classical point of view using Haralick features, a frequency point of view with generalized Fourier descriptors, and a structural point of view with Zernike moment descriptors (ZMD). These parameters are then used as inputs for a supervised classification in order to determine the most relevant. An experiment using a specific Saccharomyces cerevisiae strain presenting a fusion between a protein found in RNPs (PAB1) and the green fluorescent protein was performed to benchmark this approach. The fluorescence was observed with two-photon fluorescence microscopy. Results show that the textural approach, by mixing ZMD with Haralick features, allows for the characterization of the number of RNPs.
Identifiants
pubmed: 30757983
pii: S1431927619000084
doi: 10.1017/S1431927619000084
doi:
Substances chimiques
Poly(A)-Binding Proteins
0
Protein Aggregates
0
Ribonucleoproteins
0
Saccharomyces cerevisiae Proteins
0
pab1 protein, S cerevisiae
0
Green Fluorescent Proteins
147336-22-9
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM