| Literature DB >> 36152156 |
Álvaro González-Domínguez1, María Millán-Martínez2,3, Daniel Sánchez-Rodas2,3, Alfonso María Lechuga-Sancho1,4,5, Raúl González-Domínguez6.
Abstract
In this chapter, we describe a metallomics method based on protein precipitation under non-denaturing conditions and further analysis by inductively coupled plasma mass spectrometry for high-throughput metal speciation in plasma and erythrocyte samples. This methodology enables to study the total multielemental profile of these biological matrices, as well as to quantify the metal fractions conforming the metallometabolome and the metalloproteome. Furthermore, the analytical coverage comprises several essential and toxic metal elements, namely aluminum, arsenic, cadmium, cobalt, chromium, copper, iron, lithium, manganese, molybdenum, nickel, lead, selenium, vanadium, and zinc. Altogether, the metallomics method here proposed represents an excellent approach to comprehensively characterize the metal biodistribution in human peripheral blood, which would enable to decipher the role of metal homeostasis in health and disease, and particularly in childhood obesity.Entities:
Keywords: Childhood obesity; Erythrocytes; ICP-MS; Metals; Plasma; Size fractionation
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Year: 2023 PMID: 36152156 DOI: 10.1007/978-1-0716-2699-3_12
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745