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      Analytical methods for quantitating sulfate in plasma and serum

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          Abstract

          Circulating sulfate needs to be maintained at sufficiently high levels for healthy growth and development. Animal studies have shown the adverse physiological consequences of low circulating sulfate level on the skeletal, neurological and reproductive systems. However, sulfate is not routinely measured in clinical investigations, despite the importance of sulfate being documented over the past several decades. Several methods have been developed for measuring serum and plasma sulfate level in animals and humans, including a range of barium sulfate precipitation techniques that have been a major focus of sulfate analytics since the 1960s. Evaluation of an ion chromatography method demonstrated its utility for investigation of sulfate levels in human health. More recently, liquid chromatography-tandem mass spectrometry has been used to show hyposulfatemia in a human case of mild skeletal dysplasia. This article provides an overview of analytical methods for measuring sulfate in serum and plasma, highlighting the strengths and limitations of each method.

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          Simple, rapid, turbidometric determination of inorganic sulfate and/or protein.

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            Liquid chromatography–tandem mass spectrometry for clinical diagnostics

            Mass spectrometry is a powerful analytical tool used for the analysis of a wide range of substances and matrices; it is increasingly utilized for clinical applications in laboratory medicine. This Primer includes an overview of basic mass spectrometry concepts, focusing primarily on tandem mass spectrometry. We discuss experimental considerations and quality management, and provide an overview of some key applications in the clinic. Lastly, the Primer discusses significant challenges for implementation of mass spectrometry in clinical laboratories and provides an outlook of where there are emerging clinical applications for this technology. Tandem mass spectrometry is increasingly utilized for clinical applications in laboratory medicine. In this Primer, Thomas et al. discuss experimental considerations and quality management for implementing clinical tandem mass spectrometry in the clinic with an overview of some key applications.
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              Hyposulfatemia, growth retardation, reduced fertility, and seizures in mice lacking a functional NaSi-1 gene.

              Inorganic sulfate is required for numerous functions in mammalian physiology, and its circulating levels are proposed to be maintained by the Na+-SO42- cotransporter, (NaSi-1). To determine the role of NaSi-1 in sulfate homeostasis and the physiological consequences in its absence, we have generated a mouse lacking a functional NaSi-1 gene, Nas1. Serum sulfate concentration was reduced by >75% in Nas1-/- mice when compared with Nas1+/+ mice. Nas1-/- mice exhibit increased urinary sulfate excretion, reduced renal and intestinal Na+-SO42- cotransport, and a general growth retardation. Nas1-/- mouse body weight was reduced by >20% when compared with Nas1+/+ and Nas1+/- littermates at 2 weeks of age and remained so throughout adulthood. Nas1-/- females had a lowered fertility, with a 60% reduction in litter size. Spontaneous clonic seizures were observed in Nas1-/- mice from 8 months of age. These data demonstrate NaSi-1 is essential for maintaining sulfate homeostasis, and its expression is necessary for a wide range of physiological functions.
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                Author and article information

                Contributors
                Journal
                Essays Biochem
                Essays Biochem
                ebc
                Essays in Biochemistry
                Portland Press Ltd.
                0071-1365
                1744-1358
                December 2024
                04 December 2024
                : 68
                : 4 , Sulfation Pathways
                : 383-389
                Affiliations
                Mater Research Institute, The University of Queensland, Woolloongabba QLD, Australia
                Author notes
                Correspondence: Paul A. Dawson ( paul.dawson@ 123456mater.uq.edu.au )
                Author information
                https://orcid.org/0000-0002-7318-4985
                Article
                EBC20230092
                10.1042/EBC20230092
                11625858
                38699863
                6b169fe1-445d-4669-8505-fd816a8db62e
                © 2024 The Author(s).

                This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY). Open access for this article was enabled by the participation of University of Queensland in an all-inclusive Read & Publish agreement with Portland Press and the Biochemical Society under a transformative agreement with CAUL.

                History
                : 11 March 2024
                : 14 April 2024
                : 16 April 2024
                Page count
                Pages: 7
                Funding
                Funded by: National Health and Medical Research Council (NHMRC), doi 501100000925;
                Award ID: 2020999
                Categories
                Biochemical Techniques & Resources
                Chemical Biology
                Review Articles

                assay,biochemical pathology,method,sulfataemia,sulfate
                assay, biochemical pathology, method, sulfataemia, sulfate

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