Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/14964
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dc.contributor.authorTrenchevska, Olgicaen_US
dc.contributor.authorKamcheva, Elenaen_US
dc.contributor.authorNedelkov, Dobrinen_US
dc.date.accessioned2021-09-29T06:47:21Z-
dc.date.available2021-09-29T06:47:21Z-
dc.date.issued2011-09-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/14964-
dc.description.abstractTransthyretin (TTR, or prealbumin) is a tetrameric protein found in plasma and cerebrospinal fluid. Its major role is to transport thyroid hormones (thyroxin-T4) and retinol (through association with retinol-binding protein). TTR has been studied extensively due to the great number of point mutations that result in sequence heterogeneity. Many of these variants are associated with pathological conditions that result in extracellular deposition of amyloid fibers in tissues. In this work, we have developed a rapid mass spectrometric immunoassay for determination and quantification of TTR and its variants from human serum and plasma samples. The assay was fully characterized in terms of its precision, linearity and recovery characteristics. The new assay was also compared with a conventional TTR ELISA. Furthermore, we have applied the optimized method to analyze TTR and its modifications in 44 human plasma samples, and in the process optimized a method for TTR proteolytic digestion and identification of point mutations.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofProteomicsen_US
dc.titleMass spectrometric immunoassay for quantitative determination of transthyretin and its variantsen_US
dc.identifier.doi10.1002/pmic.201100023-
dc.identifier.urlhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fpmic.201100023-
dc.identifier.urlhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fpmic.201100023-
dc.identifier.urlhttp://onlinelibrary.wiley.com/wol1/doi/10.1002/pmic.201100023/fullpdf-
dc.identifier.volume11-
dc.identifier.issue18-
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptFaculty of Natural Sciences and Mathematics-
Appears in Collections:Faculty of Natural Sciences and Mathematics: Journal Articles
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