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Dive into the research topics where Carlos Polanco is active.

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Featured researches published by Carlos Polanco.


Computational and Mathematical Methods in Medicine | 2013

Detection of Severe Respiratory Disease Epidemic Outbreaks by CUSUM-Based Overcrowd-Severe-Respiratory-Disease-Index Model

Carlos Polanco; Jorge Alberto Castañón-González; Alejandro Macias; José Lino Samaniego; Thomas Buhse; Sebastián Villanueva-Martínez

A severe respiratory disease epidemic outbreak correlates with a high demand of specific supplies and specialized personnel to hold it back in a wide region or set of regions; these supplies would be beds, storage areas, hemodynamic monitors, and mechanical ventilators, as well as physicians, respiratory technicians, and specialized nurses. We describe an online cumulative sum based model named Overcrowd-Severe-Respiratory-Disease-Index based on the Modified Overcrowd Index that simultaneously monitors and informs the demand of those supplies and personnel in a healthcare network generating early warnings of severe respiratory disease epidemic outbreaks through the interpretation of such variables. A post hoc historical archive is generated, helping physicians in charge to improve the transit and future allocation of supplies in the entire hospital network during the outbreak. The model was thoroughly verified in a virtual scenario, generating multiple epidemic outbreaks in a 6-year span for a 13-hospital network. When it was superimposed over the H1N1 influenza outbreak census (2008–2010) taken by the National Institute of Medical Sciences and Nutrition Salvador Zubiran in Mexico City, it showed that it is an effective algorithm to notify early warnings of severe respiratory disease epidemic outbreaks with a minimal rate of false alerts.


Cell Biochemistry and Biophysics | 2014

Polar Profile of Antiviral Peptides from AVPpred Database

Carlos Polanco; José Lino Samaniego; Jorge Alberto Castañón-González; Thomas Buhse

Diseases of viral origin in humans are among the most serious threats to health and the global economy. As recent history has shown the virus has a high pandemic potential, among other reasons, due to its ability to spread by air, hence the identification, investigation, containment, and treatment of viral diseases should be considered of paramount importance. In this sense, the bioinformatics research has focused on finding fast and efficient algorithms that can identify highly toxic antiviral peptides and to serve as a first filter, so that trials in the laboratory are substantially reduced. The work presented here contributes to this effort through the use of an algorithm already published by this team, called polarity index method, which identifies with high efficiency antiviral peptides from the exhaustive analysis of the polar profile, using the linear sequence of the peptide. The test carried out included all peptides in APD2 Database and 60 antiviral peptides identified by Kumar and co-workers (Nucleic Acids Res 40:W199–204, 2012), to build its AVPpred algorithm. The validity of the method was focused on its discriminating capacity so we included the 15 sub-classifications of both Databases.


Acta Biochimica Polonica | 2017

The polar profile of ancient proteins: a computational extrapolation from prebiotics to paleobiochemistry

Carlos Polanco; Thomas Buhse; Vladimir N. Uversky; Gloria Vizcaino; Jacobo Levy Picciotto

This paper addresses the polar profile of ancient proteins using a comparative study of amino acids found in 25 000 000-year-old shells described in Abelsons work. We simulated the polar profile with a computer platform that represented an evolutionary computational toy model that mimicked the generation of small proteins starting from a pool of monomeric amino acids and that included several dynamic properties, such as self-replication and fragmentation-recombination of the proteins. The simulations were taken up to 15 generations and produced a considerable number of proteins of 25 amino acids in length. The computational model included the amino acids found in the ancient shells, the thermal degradation factor, and the relative abundance of the amino acids observed in the Miller-Urey experimental simulation of the prebiotic amino acid formation. We found that the amino acid polar profiles of the ancient shells and those simulated and extrapolated from the Miller-Urey abundances are coincident.


Acta Biochimica Polonica | 2016

Classifying lipoproteins based on their polar profiles.

Carlos Polanco; Jorge Alberto Castañón-González; Thomas Buhse; Vladimir N. Uversky; Rafael Zonana Amkie

The lipoproteins are an important group of cargo proteins known for their unique capability to transport lipids. By applying the Polarity index algorithm, which has a metric that only considers the polar profile of the linear sequences of the lipoprotein group, we obtained an analytical and structural differentiation of all the lipoproteins found in UniProt Database. Also, the functional groups of lipoproteins, and particularly of the set of lipoproteins relevant to atherosclerosis, were analyzed with the same method to reveal their structural preference, and the results of Polarity index analysis were verified by an alternate test, the Cumulative Distribution Function algorithm, applied to the same groups of lipoproteins.


Acta Biochimica Polonica | 2016

Identification of antimicrobial peptides by using eigenvectors.

Carlos Polanco

Antibacterial peptides are subject to broad research due to their potential application and the benefit they can provide for a wide range of diseases. In this work, a mathematical-computational method, called the Polarity Vector Method, is introduced that has a high discriminative level (>70%) to identify peptides associated with Gram (-) bacteria, Gram (+) bacteria, cancer cells, fungi, insects, mammalian cells, parasites, and viruses, taken from the Antimicrobial Peptides Database. This supervised method uses only eigenvectors from the incident polar matrix of the group studied. It was verified with a comparative study with another extensively verified method developed previously by our team, the Polarity Index Method. The number of positive hits of both methods was up to 98% in all the tests conducted.


Cell Biochemistry and Biophysics | 2018

On the Regularities of the Polar Profiles of Proteins Related to Ebola Virus Infection and their Functional Domains

Carlos Polanco; José Lino Samaniego Mendoza; Thomas Buhse; Vladimir N. Uversky; Ingrid Paola Bañuelos Chao; Marcela Angola Bañuelos Cedano; Fernando Michel Tavera; Daniel Michel Tavera; Manuel Falconi; Abelardo Vela Ponce de León

The number of fatalities and economic losses caused by the Ebola virus infection across the planet culminated in the havoc that occurred between August and November 2014. However, little is known about the molecular protein profile of this devastating virus. This work represents a thorough bioinformatics analysis of the regularities of charge distribution (polar profiles) in two groups of proteins and their functional domains associated with Ebola virus disease: Ebola virus proteins and Human proteins interacting with Ebola virus. Our analysis reveals that a fragment exists in each of these proteins—one named the “functional domain”—with the polar profile similar to the polar profile of the protein that contains it. Each protein is formed by a group of short sub-sequences, where each fragment has a different and distinctive polar profile and where the polar profile between adjacent short sub-sequences changes orderly and gradually to coincide with the polar profile of the whole protein. When using the charge distribution as a metric, it was observed that it effectively discriminates the proteins from their functional domains. As a counterexample, the same test was applied to a set of synthetic proteins built for that purpose, revealing that any of the regularities reported here for the Ebola virus proteins and human proteins interacting with Ebola virus were not present in the synthetic proteins. Our results indicate that the polar profile of each protein studied and its corresponding functional domain are similar. Thus, when building each protein from its functional domai—adding one amino acid at a time and plotting each time its polar profile—it was observed that the resulting graphs can be divided into groups with similar polar profiles.


Micromachines | 2017

Real Time Monitoring of Children, and Adults with Mental Disabilities Using a Low-Cost Non-Invasive Electronic Device

Carlos Polanco; Ignacio Vazquez; Adrian Martinez-Rivas; Miguel Arias-Estrada; Thomas Buhse; Juan J. Calva; Carlos Aguilar Salinas; Claudia Pimentel Hernández; Vladimir N. Uversky

There are a growing number of small children—as well as adults—with mental disabilities (including elderly citizens with Alzheimer’s disease or other forms of age-related dementia) that are getting lost in rural and urban areas for various reasons. Establishing their location within the first 72 h is crucial because lost people are exposed to all kinds of adverse conditions and in the case of the elderly, this is further aggravated if prescribed medication is needed. Herein we describe a non-invasive, low-cost electronic device that operates constantly, keeping track of time, the geographical location and the identification of the subject using it. The prototype was made using commercial low-cost electronic components. This electronic device shows high connectivity in open and closed areas and identifies the geographical location of a lost subject. We freely provide the software and technical diagrams of the prototypes.


Acta Biochimica Polonica | 2017

Non-racemic mixture model: a computational approach.

Carlos Polanco; Thomas Buhse

The behavior of a slight chiral bias in favor of l-amino acids over d-amino acids was studied in an evolutionary mathematical model generating mixed chiral peptide hexamers. The simulations aimed to reproduce a very generalized prebiotic scenario involving a specified couple of amino acid enantiomers and a possible asymmetric amplification through autocatalytic peptide self-replication while forming small multimers of a defined length. Our simplified model allowed the observation of a small ascending but not conclusive tendency in the l-amino acid over the d-amino acid profile for the resulting mixed chiral hexamers in computer simulations of 100 peptide generations. This simulation was carried out by changing the chiral bias from 1% to 3%, in three stages of 15, 50 and 100 generations to observe any alteration that could mean a drastic change in behavior. So far, our simulations lead to the assumption that under the exposure of very slight non-racemic conditions, a significant bias between l- and d-amino acids, as present in our biosphere, was unlikely generated under prebiotic conditions if autocatalytic peptide self-replication was the main or the only driving force of chiral auto-amplification.


Acta Biochimica Polonica | 2017

Electronegativity and intrinsic disorder of preeclampsia-related proteins

Carlos Polanco; Jorge Alberto Castañón-González; Vladimir N. Uversky; Thomas Buhse; José Lino Samaniego Mendoza; Juan J. Calva

Preeclampsia, hemorrhage, and infection are the leading causes of maternal death in underdeveloped countries. Since several proteins associated with preeclampsia are known, we conducted a computational study which evaluated the commonness and potential functionality of intrinsic disorder of these proteins and also made an attempt to characterize their origin. The origin of the preeclampsia-related proteins was assessed with a supervised technique, a Polarity Index Method (PIM), which evaluates the electronegativity of proteins based solely on their sequence. The commonness of intrinsic disorder was evaluated using several disorder predictors from the PONDR family, the charge-hydropathy plot (CH-plot) and cumulative distribution function (CDF) analyses, and using the MobiDB web-based tool, whereas potential functionality of intrinsic disorder was studied with the D2P2 resource and ANCHOR predictor of disorder-based binding sites, and the STRING tool was used to build the interactivity networks of the preeclampsia-related proteins. Peculiarities of the PIM-derived polar profile of the group of preeclampsia-related proteins were then compared with profiles of a group of lipoproteins, antimicrobial peptides, angiogenesis-related proteins, and the intrinsically disordered proteins. Our results showed a high graphical correlation between preeclampsia proteins, lipoproteins, and the angiogenesis proteins. We also showed that many preeclampsia-related proteins contain numerous functional disordered regions. Therefore, these bioinformatics results led us to assume that the preeclampsia proteins are highly associated with the lipoproteins group, and that some preeclampsia-related proteins contain significant amounts of functional disorders.


International Scholarly Research Notices | 2012

Effect of Nitrogen and Periphyton Extract on the Growth of Nostocsphaericum in Cultures

Itzel Becerra-Absal; Thomas Buhse; Carlos Polanco; Rosaluz Tavera

Nostoc sphaericum shows marked growth differences in two Mexican wetland ecosystems consisting of rain forest and tropical deciduous forest, respectively. The amount of nitrogen and periphyton extract dominated by other Cyanoprokaryota had been identified as the most obvious differences between these two ecosystems. We studied the impact of these variables on the physiology and morphology of N. sphaericum. that is, the chlorophyll-a content of the thalli and the changes in the size of the trichomes as well as the cell division rate. Our results combined with a statistical verification indicate that the cell division rate of N. sphaericum with solid media is neither stimulated by nitrogen nor by accompanying cyanoprokaryotes and therefore is assumed to have no impact on the thalli observed in situ. However, these two variables are affecting the size of both the trichomes and the thalli, thus suggested to cause the observed growth differences between the two wetlands.

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Thomas Buhse

Universidad Autónoma del Estado de Morelos

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José Lino Samaniego

National Autonomous University of Mexico

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José Lino Samaniego Mendoza

National Autonomous University of Mexico

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A. Negrón-Mendoza

National Autonomous University of Mexico

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Abelardo Vela Ponce de León

National Autonomous University of Mexico

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Alicia Negron

National Autonomous University of Mexico

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Daniel Michel Tavera

National Autonomous University of Mexico

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F. G. Mosqueira

National Autonomous University of Mexico

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