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               <dc:title>Analysis of serum transthyretin by on-line immunoaffinity solid-phase extraction capillary electrophoresis mass spectrometry using magnetic beads</dc:title>
               <dc:creator>Peró Gascón, Roger</dc:creator>
               <dc:creator>Pont Villanueva, Laura</dc:creator>
               <dc:creator>Benavente Moreno, Fernando J. (Julián)</dc:creator>
               <dc:creator>Barbosa Torralbo, José</dc:creator>
               <dc:creator>Sanz Nebot, María Victoria</dc:creator>
               <dc:subject>Electroforesi capil·lar</dc:subject>
               <dc:subject>Espectrometria de masses</dc:subject>
               <dc:subject>Camps magnètics</dc:subject>
               <dc:subject>Capillary electrophoresis</dc:subject>
               <dc:subject>Mass spectrometry</dc:subject>
               <dc:subject>Magnetic fields</dc:subject>
               <dc:description>In this paper, an on-line immunoaffinity solid-phase extraction capillary electrophoresis mass spectrometry (IA-SPE-CE-MS) method using magnetic beads (MBs) is described for the analysis of serum transthyretin (TTR), which is a protein related to different types of amyloidosis. First, purification of TTR from serum was investigated by off-line immunoprecipitation and CE-MS. The suitability of three Protein A (ProA) MBs (Protein A Ultrarapid AgaroseTM (UAPA), Dynabeads® Protein A (DyPA) and SiMAG-Protein A (SiPA)) and AffiAmino Ultrarapid AgaroseTM (UAAF) MBs to prepare an IA sorbent with a polyclonal antibody (Ab) against TTR, was studied. In all cases results were repeatable and it was possible the identification and the quantitation of the relative abundance of the 6 most abundant TTR proteoforms. Although recoveries were the best with UAPA MBs, UAAF MBs were preferred for on-line immunopurification because Ab was not eluted from the MBs. Under the optimised conditions with standards in IA-SPE-CE-MS, microcartridge lifetime (>20 analyses/day) and repeatability (2.9 and 4.3 % RSD for migration times and peak areas) were good, the method was linear between 5- 25 µg·mL-1 and limit of detection (LOD) was around 1 µg·mL-1 (25 times lower than by CE-MS, 25 µg·mL-1). A simple off-line sample pretreatment based on precipitation of the most abundant proteins with 5% (v/v) of phenol was necessary to clean-up serum samples. The potential of the on-line method to screen for familial amyloidotic polyneuropathy type I (FAP-I), which is the most common hereditary systemic amyloidosis, was demonstrated analysing serum samples from healthy controls and FAP-I patients.</dc:description>
               <dc:date>2018-06-21T14:04:35Z</dc:date>
               <dc:date>2018-06-21T14:04:35Z</dc:date>
               <dc:date>2016</dc:date>
               <dc:date>2018-06-21T14:04:36Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
               <dc:relation>Versió postprint del document publicat a: https://doi.org/10.1002/elps.201500495</dc:relation>
               <dc:relation>Electrophoresis, 2016, vol. 37, p. 1220-1231</dc:relation>
               <dc:relation>https://doi.org/10.1002/elps.201500495</dc:relation>
               <dc:rights>(c) Wiley-VCH, 2016</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Wiley-VCH</dc:publisher>
               <dc:source>Articles publicats en revistes  (Enginyeria Química i Química Analítica)</dc:source>
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