<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-01T01:09:59Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/98453" metadataPrefix="oai_dc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/98453</identifier><datestamp>2025-03-06T15:23:03Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_18</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Cytoplasmic Calcium Buffering: An Integrative Crosstalk.</dc:title>
   <dc:creator>Gilabert Santos, Juan Antonio</dc:creator>
   <dc:contributor>Springer Nature</dc:contributor>
   <dc:subject>61</dc:subject>
   <dc:subject>Ca2+ buffering</dc:subject>
   <dc:subject>Immobile buffers</dc:subject>
   <dc:subject>Mobile buffers</dc:subject>
   <dc:subject>Modeling Ca2+ signaling</dc:subject>
   <dc:subject>Ciencias Biomédicas</dc:subject>
   <dc:subject>2403 Bioquímica</dc:subject>
   <dc:description>Calcium (Ca2+) buffering is part of an integrative crosstalk between different mechanisms and elements involved in the control of free Ca2+ ions persistence in the cytoplasm and hence, in the Ca2+-dependence of many intracellular processes. Alterations of Ca2+ homeostasis and signaling from systemic to subcellular levels also play a pivotal role in the pathogenesis of many diseases. Compared with Ca2+ sequestration towards intracellular Ca2+ stores, Ca2+ buffering is a rapid process occurring in a subsecond scale. Any molecule (or binding site) with the ability to bind Ca2+ ions could be considered, at least in principle, as a buffer. However, the term Ca2+ buffer is applied only to a small subset of Ca2+ binding proteins containing acidic side-chain residues. Ca2+ buffering in the cytoplasm mainly relies on mobile and immobile or fixed buffers controlling the diffusion of free Ca2+ ions inside the cytosol both temporally and spatially. Mobility of buffers depends on their molecular weight, but other parameters as their concentration, affinity for Ca2+ or Ca2+ binding and dissociation kinetics next to their diffusional mobility also contribute to make Ca2+ signaling one of the most complex signaling activities of the cell. The crosstalk between all the elements involved in the intracellular Ca2+ dynamics is a process of extreme complexity due to the diversity of structural and molecular elements involved but permit a highly regulated spatiotemporal control of the signal mediated by Ca2+ ions. The basis of modeling tools to study Ca2+ dynamics are also presented.</dc:description>
   <dc:description>Depto. de Farmacología y Toxicología</dc:description>
   <dc:description>Fac. de Veterinaria</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:date>2024-02-02T17:02:43Z</dc:date>
   <dc:date>2024-02-02T17:02:43Z</dc:date>
   <dc:date>2020</dc:date>
   <dc:type>book part</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/98453</dc:identifier>
   <dc:identifier>0065-2598</dc:identifier>
   <dc:identifier>10.1007/978-3-030-12457-1_7</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>metadata only access</dc:rights>
   <dc:publisher>Springer</dc:publisher>
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