A computational intelligence analysis of G proteincoupled receptor sequinces for pharmacoproteomic applications

Arguably, drug research has contributed more to the progress of medicine during the past decades than any other scientific factor. One of the main areas of drug research is related to the analysis of proteins. The world of pharmacology is becoming increasingly dependent on the advances in the fields of genomics and proteomics. This dependency brings about the challenge of finding robust methods to analyze the complex data they generate. Such challenge invites us to go one step further than traditional statistics and resort to approaches under the conceptual umbrella of artificial intelligence, including machine learning (ML), statistical pattern recognition and soft computing methods. Sound statistical principles are essential to trust the evidence base built through the use of such approaches. Statistical ML methods are thus at the core of the current thesis. More than 50% of drugs currently available target only four key protein families, from which almost a 30% correspond to the G Protein-Coupled Receptors (GPCR) superfamily. This superfamily regulates the function of most cells in living organisms and is at the centre of the investigations reported in the current thesis. No much is known about the 3D structure of these proteins. Fortunately, plenty of information regarding their amino acid sequences is readily available. The automatic grouping and classification of GPCRs into families and these into subtypes based on sequence analysis may significantly contribute to ascertain the pharmaceutically relevant properties of this protein superfamily. There is no biologically-relevant manner of representing the symbolic sequences describing proteins using real-valued vectors. This does not preclude the possibility of analyzing them using principled methods. These may come, amongst others, from the field of statisticalML. Particularly, kernel methods can be used to this purpose. Moreover, the visualization of high-dimensional protein sequence data can be a key exploratory tool for finding meaningful information that might be obscured by their intrinsic complexity. That is why the objective of the research described in this thesis is twofold: first, the design of adequate visualization-oriented artificial intelligence-based methods for the analysis of GPCR sequential data, and second, the application of the developed methods in relevant pharmacoproteomic problems such as GPCR subtyping and protein alignment-free analysis.Se podría decir que la investigación farmacológica ha desempeñado un papel predominante en el avance de la medicina a lo largo de las últimas décadas. Una de las áreas principales de investigación farmacológica es la relacionada con el estudio de proteínas. La farmacología depende cada vez más de los avances en genómica y proteómica, lo que conlleva el reto de diseñar métodos robustos para el análisis de los datos complejos que generan. Tal reto nos incita a ir más allá de la estadística tradicional para recurrir a enfoques dentro del campo de la inteligencia artificial, incluyendo el aprendizaje automático y el reconocimiento de patrones estadístico, entre otros. El uso de principios sólidos de teoría estadística es esencial para confiar en la base de evidencia obtenida mediante estos enfoques. Los métodos de aprendizaje automático estadístico son uno de los fundamentos de esta tesis. Más del 50% de los fármacos en uso hoy en día tienen como ¿diana¿ apenas cuatro familias clave de proteínas, de las que un 30% corresponden a la super-familia de los G-Protein Coupled Receptors (GPCR). Los GPCR regulan la funcionalidad de la mayoría de las células y son el objetivo central de la tesis. Se desconoce la estructura 3D de la mayoría de estas proteínas, pero, en cambio, hay mucha información disponible de sus secuencias de amino ácidos. El agrupamiento y clasificación automáticos de los GPCR en familias, y de éstas a su vez en subtipos, en base a sus secuencias, pueden contribuir de forma significativa a dilucidar aquellas de sus propiedades de interés farmacológico. No hay forma biológicamente relevante de representar las secuencias simbólicas de las proteínas mediante vectores reales. Esto no impide que se puedan analizar con métodos adecuados. Entre estos se cuentan las técnicas provenientes del aprendizaje automático estadístico y, en particular, los métodos kernel. Por otro lado, la visualización de secuencias de proteínas de alta dimensionalidad puede ser una herramienta clave para la exploración y análisis de las mismas. Es por ello que el objetivo central de la investigación descrita en esta tesis se puede desdoblar en dos grandes líneas: primero, el diseño de métodos centrados en la visualización y basados en la inteligencia artificial para el análisis de los datos secuenciales correspondientes a los GPCRs y, segundo, la aplicación de los métodos desarrollados a problemas de farmacoproteómica tales como la subtipificación de GPCRs y el análisis de proteinas no-alineadas

Exploratory visualization of misclassified GPCRs from their transformed unaligned sequences using manifold learning techniques

Class C G-protein-coupled receptors (GPCRs) are cell membrane proteins of great relevance to biology and pharmacology. Previous research has revealed an upper boundary on the accuracy that can be achieved in their classification into subtypes from the unaligned transformation of their sequences. To investigate this, we focus on sequences that have been misclassified using supervised methods. These are visualized, using a nonlinear dimensionality reduction technique and phylogenetic trees, and then characterized against the rest of the data and, particularly, against the rest of cases of their own subtype. This should help to discriminate between different types of misclassification and to build hypotheses about database quality problems and the extent to which GPCR sequence transformations limit subtype discriminability. The reported experiments provide a proof of concept for the proposed method.Postprint (published version

Development of a model to estimate the effective second moment of area of one-way reinforced concrete flexural elements

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Visual interpretation of class C GPCR subtype overlapping from the nonlinear mapping of transformed primary sequences

This brief paper addresses the problem of visually assessing the natural discriminability of the different subtypes that characterize class C G-Protein-Coupled Receptors, which are membrane proteins of interest in pharmacology, from diverse transformations of their primary amino acid sequences. Visualization, achieved using nonlinear dimensionality reduction techniques, is used as an exploratory tool to increase the interpretability of the data subtype structure. Combined with a quantitative estimation of subtype overlapping, this approach should be of help to experts in proteomics.Peer Reviewe

A study of the signal-averaged electrocardiogram in acute myocardial infarction and its value for the prediction of subsequent arrhythmic events and sudden cardiac death in the thrombolytic era A prospective study

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Manifold learning visualization of metabotropic glutamate receptors

G-Protein-Coupled Receptors (GPCRs) are cell membrane proteins with a key role in biological processes. GPCRs of class C, in particular, are of great interest in pharmacology. The lack of knowledge about their 3-D structures means they must be investigated through their primary amino acid sequences. Sequence visualization can help to explore the existing receptor sub-groupings at different partition levels. In this paper, we focus on Metabotropic Glutamate Receptors (mGluR), a subtype of class C GPCRs. Different versions of a probabilistic manifold learning model are employed to comparatively sub-group and visualize them through different transformations of their sequences.Peer Reviewe

Exploratory visualization of misclassified GPCRs from their transformed unaligned sequences using manifold learning techniques

Class C G-protein-coupled receptors (GPCRs) are cell membrane proteins of great relevance to biology and pharmacology. Previous research has revealed an upper boundary on the accuracy that can be achieved in their classification into subtypes from the unaligned transformation of their sequences. To investigate this, we focus on sequences that have been misclassified using supervised methods. These are visualized, using a nonlinear dimensionality reduction technique and phylogenetic trees, and then characterized against the rest of the data and, particularly, against the rest of cases of their own subtype. This should help to discriminate between different types of misclassification and to build hypotheses about database quality problems and the extent to which GPCR sequence transformations limit subtype discriminability. The reported experiments provide a proof of concept for the proposed method

Loan loss provision by international banks Estimation, determinants and evidence

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Visual characterization of misclassified Class C GPCRs through Manifold-based machine learning methods

G-protein-coupled receptors are cell membrane proteins of great interest in biology and pharmacology. Previous analysis of Class C of these receptors has revealed the existence of an upper boundary on the accuracy that can be achieved in the classification of their standard subtypes from the unaligned transformation of their primary sequences. To further investigate this apparent boundary, the focus of the analysis in this paper is placed on receptor sequences that were previously misclassified using supervised learning methods. In our experiments, these sequences are visualized using a nonlinear dimensionality reduction technique and phylogenetic trees. They are subsequently characterized against the rest of the data and, particularly, against the rest of cases of their own subtype. This exploratory visualization should help us to discriminate between different types of misclassification and to build hypotheses about database quality problems and the extent to which GPCR sequence transformations limit subtype discriminability. The reported experiments provide a proof of concept for the proposed method.Peer Reviewe

Exploratory visualization of misclassified GPCRs from their transformed unaligned sequences using manifold learning techniques

Class C G-protein-coupled receptors (GPCRs) are cell membrane proteins of great relevance to biology and pharmacology. Previous research has revealed an upper boundary on the accuracy that can be achieved in their classification into subtypes from the unaligned transformation of their sequences. To investigate this, we focus on sequences that have been misclassified using supervised methods. These are visualized, using a nonlinear dimensionality reduction technique and phylogenetic trees, and then characterized against the rest of the data and, particularly, against the rest of cases of their own subtype. This should help to discriminate between different types of misclassification and to build hypotheses about database quality problems and the extent to which GPCR sequence transformations limit subtype discriminability. The reported experiments provide a proof of concept for the proposed method