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1.
J Struct Biol ; 195(1): 123-8, 2016 07.
Artigo em Inglês | MEDLINE | ID: mdl-27102900

RESUMO

Macromolecular complexes perform their physiological functions by local rearrangements of their constituents and biochemically interacting with their reaction partners. These rearrangements may involve local rotations and the induction of local strains causing different mechanical efforts and stretches at the different areas of the protein. The analysis of these local deformations may reveal important insight into the way proteins perform their tasks. In this paper we introduce a method to perform this kind of local analysis using Electron Microscopy volumes in a fully objective and automatic manner. For doing so, we exploit the continuous nature of the result of an elastic image registration using B-splines as its basis functions. We show that the results obtained by the new automatic method are consistent with previous observations on these macromolecules.


Assuntos
Substâncias Macromoleculares/química , Microscopia Eletrônica/métodos , Trifosfato de Adenosina/química , Algoritmos , Automação , Proteínas de Bactérias/química , Fenômenos Biomecânicos , Chaperonina 60/química , Proteínas de Choque Térmico/química , Humanos , Ribossomos Mitocondriais/química , Modelos Teóricos , Chaperonas Moleculares/química , Ligação Proteica , Rotação
2.
Bioinformatics ; 29(19): 2460-8, 2013 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-23958728

RESUMO

MOTIVATION: Structural information of macromolecular complexes provides key insights into the way they carry out their biological functions. Achieving high-resolution structural details with electron microscopy requires the identification of a large number (up to hundreds of thousands) of single particles from electron micrographs, which is a laborious task if it has to be manually done and constitutes a hurdle towards high-throughput. Automatic particle selection in micrographs is far from being settled and new and more robust algorithms are required to reduce the number of false positives and false negatives. RESULTS: In this article, we introduce an automatic particle picker that learns from the user the kind of particles he is interested in. Particle candidates are quickly and robustly classified as particles or non-particles. A number of new discriminative shape-related features as well as some statistical description of the image grey intensities are used to train two support vector machine classifiers. Experimental results demonstrate that the proposed method: (i) has a considerably low computational complexity and (ii) provides results better or comparable with previously reported methods at a fraction of their computing time. AVAILABILITY: The algorithm is fully implemented in the open-source Xmipp package and downloadable from http://xmipp.cnb.csic.es.


Assuntos
Automação Laboratorial/métodos , Microscopia Eletrônica , Adenoviridae/ultraestrutura , Algoritmos , DNA Helicases/ultraestrutura , Processamento de Imagem Assistida por Computador/métodos , Substâncias Macromoleculares , Tamanho da Partícula
3.
J Struct Biol ; 183(3): 342-353, 2013 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-23933392

RESUMO

Three-dimensional reconstruction of biological specimens using electron microscopy by single particle methodologies requires the identification and extraction of the imaged particles from the acquired micrographs. Automatic and semiautomatic particle selection approaches can localize these particles, minimizing the user interaction, but at the cost of selecting a non-negligible number of incorrect particles, which can corrupt the final three-dimensional reconstruction. In this work, we present a novel particle quality assessment and sorting method that can separate most erroneously picked particles from correct ones. The proposed method is based on multivariate statistical analysis of a particle set that has been picked previously using any automatic or manual approach. The new method uses different sets of particle descriptors, which are morphology-based, histogram-based and signal to noise analysis based. We have tested our proposed algorithm with experimental data obtaining very satisfactory results. The algorithm is freely available as a part of the Xmipp 3.0 package [http://xmipp.cnb.csic.es].


Assuntos
Imageamento Tridimensional , Software , Adenovírus Humanos/ultraestrutura , Algoritmos , Inteligência Artificial , Microscopia Crioeletrônica/métodos , Hemocianinas/ultraestrutura , Análise Multivariada , Razão Sinal-Ruído
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