Volume 15, Issue 7
Dataset Brief

Exploring analytical proteomics platforms toward the definition of human cardiac stem cells receptome

Patrícia Gomes‐Alves

iBET, Instituto de Biologia Experimental e Tecnológica, Oeiras, Portugal

Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Oeiras, Portugal

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Margarida Serra

iBET, Instituto de Biologia Experimental e Tecnológica, Oeiras, Portugal

Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Oeiras, Portugal

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Catarina Brito

iBET, Instituto de Biologia Experimental e Tecnológica, Oeiras, Portugal

Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Oeiras, Portugal

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Luis R.‐Borlado

Coretherapix, Tres‐Cantos, Madrid, Spain

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Juan A. López

Laboratorio de Proteómica Cardiovascular and Unidad de Proteómica, Centro Nacional de Investigaciones Cardiovasculares, Madrid, Spain

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Jesús Vázquez

Laboratorio de Proteómica Cardiovascular and Unidad de Proteómica, Centro Nacional de Investigaciones Cardiovasculares, Madrid, Spain

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Manuel J. T. Carrondo

iBET, Instituto de Biologia Experimental e Tecnológica, Oeiras, Portugal

Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Oeiras, Portugal

Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Monte da Caparica, Portugal

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António Bernad

Centro Nacional de Biotecnología, Madrid, Spain

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Paula M. Alves

Corresponding Author

iBET, Instituto de Biologia Experimental e Tecnológica, Oeiras, Portugal

Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Oeiras, Portugal

Correspondence: Professor Paula M. Alves, ITQB‐UNL/iBET, Apartado 12, 2781‐901 Oeiras, Portugal

E‐mail: marques@ibet.pt

Fax: +351 214421161

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First published: 12 December 2014
Citations: 10

Abstract

Human cardiac stem cells (hCSC) express a portfolio of plasma membrane receptors that are involved in the regulatory auto/paracrine feedback loop mechanism of activation of these cells, and consequently contribute to myocardial regeneration. In order to attain a comprehensive description of hCSC receptome and overcoming the inability demonstrated by other technologies applied in receptor identification, mainly due to the transmembrane nature, high hydrophobic character and relative low concentration of these proteins, we have exploited and improved a proteomics workflow. This approach was based on the enrichment of hCSC plasma membrane fraction and addition of prefractionation steps prior to MS analysis. More than 100 plasma membrane receptors were identified. The data reported herein constitute a valuable source of information to further understand cardiac stem cells activation mechanisms and the subsequent cardiac repair process. All MS data have been deposited in the ProteomeXchange with identifier PXD001117 (http://proteomecentral.proteomexchange.org/dataset/PXD001117).

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