<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1405-888X</journal-id>
<journal-title><![CDATA[TIP. Revista especializada en ciencias químico-biológicas]]></journal-title>
<abbrev-journal-title><![CDATA[TIP]]></abbrev-journal-title>
<issn>1405-888X</issn>
<publisher>
<publisher-name><![CDATA[Universidad Nacional Autónoma de México, Facultad de Estudios Superiores Zaragoza]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1405-888X2019000100203</article-id>
<article-id pub-id-type="doi">10.22201/fesz.23958723e.2018.0.163</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Microdominios membranales bacterianos semejantes a balsas lipídicas]]></article-title>
<article-title xml:lang="en"><![CDATA[Lipid raft-like bacterial membrane microdomains]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Guzmán-Flores]]></surname>
<given-names><![CDATA[José E.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Georgellis]]></surname>
<given-names><![CDATA[Dimitris]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Álvarez]]></surname>
<given-names><![CDATA[Adrián F.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Nacional Autónoma de México Instituto de Fisiología Celular Departamento de Genética Molecular]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2019</year>
</pub-date>
<volume>22</volume>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1405-888X2019000100203&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1405-888X2019000100203&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1405-888X2019000100203&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen La capacidad de las membranas biológicas para compartimentar diversos procesos fisiológicos como la transducción de señales, tráfico vesicular, entre otros, ha llevado al estudio de estructuras conocidas como balsas lipídicas o microdominios de membrana. Estos microdominios se componen de proteínas y lípidos especializados, los cuales han sido ampliamente descritos en una gran variedad de células eucariotas. Una característica de las balsas lipídicas es el alto grado de empaquetamiento de sus componentes, lo que genera una menor fluidez con respecto al resto de la membrana. La técnica más empleada para caracterizar estos microdominios, es la generación de membranas resistentes a detergentes (DRM-Detergent-ResistantMembranes), la cual aprovecha las características físico-químicas de las balsas lipídicas, cuyos componentes estructurales son resistentes a la solubilización por detergentes. Las proteínas que contienen un dominio conocido como SPFH (Stomatin, Prohibitin, Flotillin, HflK/C) son consideradas como marcadores de balsas lipídicas y se identifican frecuentemente en preparaciones de DRM. Recientemente, la amplia distribución de proteínas con dominios SPFH codificadas en cromosomas bacterianos, ha dirigido el enfoque al estudio de estructuras similares a balsas lipídicas en las membranas bacterianas. En esta revisión se exponen algunos avances recientes en la identificación y estudio de los microdominios de membrana bacterianos similares a balsas lipídicas presentes en eucariontes.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract The capacity of biological membranes to compartmentalize various physiological processes such as signal transduction, vesicular traffic, among others, has led to the study of structures known as lipid rafts or membrane microdomains. These microdomains are made of specialized proteins and lipids, which have been widely described in a broad variety of eukaryotic cells. A feature of lipid rafts is the high degree of packaging of their components, which generates less fluidity with respect to the rest of the membrane. The most commonly used technique to characterize these microdomains is the generation of Detergent-Resistant Membranes (DRM), which takes advantage of the physico-chemical characteristics of lipid rafts, whose structural components are resistant to solubilization by detergents. SPFH-domain containing proteins (Stomatin, Prohibitin, Flotillin, HflK/C) are frequently found in DRM preparations and are commonly used as lipid rafts markers. Recently, the widely distribution of SPHF-containing proteins encoded in bacterial chromosomes, has directed our attention to the study of lipid raft-like microdomains in bacterial membranes. In this review, we present some recent advances on the identification and analysis of bacterial lipid raft-like membrane microdomains.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[bacteria]]></kwd>
<kwd lng="es"><![CDATA[balsas lipídicas]]></kwd>
<kwd lng="es"><![CDATA[membranas resistentes a detergentes]]></kwd>
<kwd lng="es"><![CDATA[flotilina]]></kwd>
<kwd lng="en"><![CDATA[bacteria]]></kwd>
<kwd lng="en"><![CDATA[lipid rafts]]></kwd>
<kwd lng="en"><![CDATA[detergent-resistant membranes]]></kwd>
<kwd lng="en"><![CDATA[flotillin]]></kwd>
</kwd-group>
</article-meta>
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