Jose Luis Vilas
Spanish National Research Council
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Featured researches published by Jose Luis Vilas.
Applied Optics | 2013
Jose Luis Vilas; Luis Miguel Sanchez-Brea; Eusebio Bernabeu
Two plates of different birefringence material can be combined to obtain an achromatic wave retarder. In this work, we achieve a correction for the overall retardation of the system that extends the relation to any azimuth. Current techniques for the design of achromatic wave retarders do not present a parameter that characterizes its achromatism on a range of wavelengths. Thus, an achromatic degree has been introduced, in order to determine the optimal achromatic design composed with retarder plates for a spectrum of incident light. In particular, we have optimized a quarter retarder using two wave plates for the visible spectrum. Our technique has been compared to previous results, showing significant improvement.
Applied Optics | 2016
Jose Luis Vilas; José A. Sanchez-Martin; Eusebio Bernabeu
The temperature dependence of the birefringence in a suspended core fiber (SCF) has been experimentally analyzed by using a polarimetric setup. The used configuration consists of two linear polarizers and the SCF as birefringent medium. A theoretical study based on Jones matrices has been carried out to analyze the experimental observed behavior. For this, a polarimetric all-fiber configuration was used whose sensitivity depends on the wavelength variation with temperature. Results obtained show that it is strongly affected when the air holes of SCF are partially filled with ethanol.
BioMed Research International | 2017
Carlos Oscar S. Sorzano; Javier Vargas; Joaquín Otón; J. M. de la Rosa-Trevín; Jose Luis Vilas; Mohsen Kazemi; Roberto Melero; L. del Cano; Jesús Cuenca; P. Conesa; Josué Gómez-Blanco; Roberto Marabini; J.M. Carazo
One of the key steps in Electron Microscopy is the tomographic reconstruction of a three-dimensional (3D) map of the specimen being studied from a set of two-dimensional (2D) projections acquired at the microscope. This tomographic reconstruction may be performed with different reconstruction algorithms that can be grouped into several large families: direct Fourier inversion methods, back-projection methods, Radon methods, or iterative algorithms. In this review, we focus on the latter family of algorithms, explaining the mathematical rationale behind the different algorithms in this family as they have been introduced in the field of Electron Microscopy. We cover their use in Single Particle Analysis (SPA) as well as in Electron Tomography (ET).
Applied Optics | 2014
Jose Luis Vilas; Eusebio Bernabeu; Luis Miguel Sanchez-Brea; Rafael Espinosa-Luna
The generation of circularly polarized light with a high circularity degree and low azimuthal error sensitivity was analyzed using a system composed by two waveplates. It is shown how the high circularity degree is achieved using a combination of a half- (λ/2) and a quarter- (λ/4) waveplate λ/2+λ/4 configuration. However, the lowest azimuthal sensitivity under small variations in the azimuths of the waveplates is obtained by employing a λ/4+λ/2 configuration. Analytical calculus particularized for quartz and MgF₂ waveplates is presented.
bioRxiv | 2018
Erney Ramírez-Aportela; Jose Luis Vilas; Roberto Melero; P. Conesa; Marta Martínez; David Maluenda; Javier Mota; Amaya Jimenez; Javier Vargas; Roberto Marabini; José María Carazo; Carlos Oscar S. Sorzano
Recent technological advances and computational developments, have allowed the reconstruction of cryo-EM maps at near-atomic resolution structures. Cryo-EM maps benefit significantly of a “postprocessing” step, normally referred to as “sharpening”, that tends to increase signal at medium/high resolution. Here, we propose a new method for local sharpening of volumes generated by cryo-EM. The algorithm (LocalDeblur) is based on a local resolution-guided Wiener restoration approach, does not need any prior atomic model and it avoids artificial structure 1 factor corrections. LocalDeblur is fully automatic and parameter free. We show that the new method significantly and quantitatively improving map quality and interpretability, especially in cases of broad local resolution changes (as is often the case of membrane proteins).
Journal of Structural Biology | 2018
Josué Gómez-Blanco; J.M. de la Rosa-Trevín; Roberto Marabini; L. del Cano; A. Jiménez; María Jesús Martínez; Roberto Melero; T. Majtner; D. Maluenda; J. Mota; Y. Rancel; E. Ramírez-Aportela; Jose Luis Vilas; M. Carroni; S. Fleischmann; E. Lindahl; A.W. Ashton; M. Basham; D.K. Clare; K. Savage; C.A. Siebert; G.G. Sharov; Carlos Oscar S. Sorzano; P. Conesa; J.M. Carazo
Three dimensional electron microscopy is becoming a very data-intensive field in which vast amounts of experimental images are acquired at high speed. To manage such large-scale projects, we had previously developed a modular workflow system called Scipion (de la Rosa-Trevín et al., 2016). We present here a major extension of Scipion that allows processing of EM images while the data is being acquired. This approach helps to detect problems at early stages, saves computing time and provides users with a detailed evaluation of the data quality before the acquisition is finished. At present, Scipion has been deployed and is in production mode in seven Cryo-EM facilities throughout the world.
Journal of Structural Biology | 2018
Carlos Oscar S. Sorzano; E. Fernández-Giménez; V. Peredo-Robinson; Javier Vargas; T. Majtner; G. Caffarena; Joaquín Otón; Jose Luis Vilas; J.M. de la Rosa-Trevín; Roberto Melero; Josué Gómez-Blanco; Jesús Cuenca; L. del Cano; P. Conesa; Roberto Marabini; J.M. Carazo
The introduction of Direct Electron Detector (DED) videos in the Electron Microscope field has boosted Single Particle Analysis to a point in which it is currently considered to be a key technique in Structural Biology. In this article we introduce an approach to estimate the DED camera gain at each pixel from the movies themselves. This gain is needed to have the set of recorded frames into a coherent gray level range, homogeneous over the whole image. The algorithm does not need any other input than the DED movie itself, being capable of providing an estimate of the camera gain image, helping to identify dead pixels and cases of incorrectly calibrated cameras. We propose the algorithm to be used either to validate the experimentally acquired gain image (for instance, to follow its possible change over time) or to verify that there is no residual gain image after experimentally correcting for the camera gain. We show results for a number of DED camera models currently in use (DE, Falcon II, Falcon 3, and K2).
Journal of Structural Biology | 2018
Carlos Oscar S. Sorzano; Javier Vargas; J.M. de la Rosa-Trevín; A. Jiménez; D. Maluenda; Roberto Melero; María Jesús Martínez; E. Ramírez-Aportela; P. Conesa; Jose Luis Vilas; Roberto Marabini; J.M. Carazo
The Map Challenge organized by the Electron Microscopy Data Bank has prompted the development of an Xmipp high resolution reconstruction protocol (which we will refer to as highres) that is integrated in the software platform Scipion. In this work we describe the details of the image angular alignment and map reconstruction steps in our new method. This algorithm is similar to the standard projection matching approach with some important modifications, especially in the area of detecting significant features in the reconstructed volume. We show that the new method is able to produce higher resolution maps than the current de facto standard as measured by the Fourier Shell Correlation, the Monogenic Local Resolution and EMRinger.
Journal of Structural Biology | 2016
Jose Luis Vilas; J. Navas; Josué Gómez-Blanco; J.M. de la Rosa-Trevín; Roberto Melero; I. Peschiera; I. Ferlenghi; Jesús Cuenca; Roberto Marabini; J.M. Carazo; Javier Vargas; Carlos Oscar S. Sorzano
Random conical tilt (RCT) and orthogonal tilt reconstruction (OTR) are two remarkable methods for reconstructing the three-dimensional structure of macromolecules at low resolution. These techniques use two images at two different sample tilts. One of the most demanding steps in these methods at the image processing level is to identify corresponding particles on both micrographs, and manual or semiautomatic matching methods are usually used. Here we present an approach to solve this bottleneck with a fully automatic method for assigning particle tilt pairs. This new algorithm behaves correctly with a variety of samples, covering the range from small to large macromolecules and from sparse to densely populated fields of view. It is also more rapid than previous approaches. The roots of the method lie in a Delaunay triangulation of the set of independently picked coordinates on both the untilted and tilted micrographs. These triangulations are then used to search an affine transformation between the untilted and tilted triangles. The affine transformation that maximizes the number of correspondences between the two micrographs defines the coordinate matching.
Journal of Structural Biology | 2016
Carlos Oscar S. Sorzano; A. Martín-Ramos; F. Prieto; Roberto Melero; Jaime Martín-Benito; Slavica Jonic; J. Navas-Calvente; Javier Vargas; Joaquín Otón; V. Abrishami; J.M. de la Rosa-Trevín; Josué Gómez-Blanco; Jose Luis Vilas; Roberto Marabini; J.M. Carazo
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.