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Structural typing of systemic amyloidoses by luminescent-conjugated polymer spectroscopy.

Nilsson, Peter (author)
Linköpings universitet,Organisk Kemi,Tekniska högskolan
Ikenberg, Kristian (author)
University Hospital of Zurich
Åslund, Andreas, 1978- (author)
Linköpings universitet,Organisk Kemi,Tekniska högskolan
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Fransson, Sophia (author)
Konradsson, Peter (author)
Linköpings universitet,Organisk Kemi,Tekniska högskolan
Röcken, Christoph (author)
Christian-Albrechts-University, Kiel
Moch, Holger (author)
University Hospital of Zurich
Aguzzi, Adriano (author)
University Hospital of Zurich
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 (creator_code:org_t)
Elsevier BV, 2010
2010
English.
In: The American journal of pathology. - : Elsevier BV. - 1525-2191 .- 0002-9440. ; 176:2, s. 563-574
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Most systemic amyloidoses are progressive and lethal, and their therapy depends on the identification of the offending proteins. Here we report that luminescent-conjugated thiophene polymers (LCP) sensitively detect amyloid deposits. The heterodisperse polythiophene acetic acid derivatives, polythiophene acetic acid (PTAA) and trimeric PTAA, emitted yellow-red fluorescence on binding to amyloid deposits, whereas chemically homogeneous pentameric formic thiophene acetic acid emitted green-yellow fluorescence. The geometry of LCPs modulates the spectral composition of the emitted light, thereby reporting ligand-induced steric changes. Accordingly, a screen of PTAA-stained amyloid deposits in histological tissue arrays revealed striking spectral differences between specimens. Blinded cluster assignments of spectral profiles of tissue samples from 108 tissue samples derived from 96 patients identified three nonoverlapping classes, which were found to match AA, AL, and ATTR immunotyping. We conclude that LCP spectroscopy is a sensitive and powerful tool for identifying and characterizing amyloid deposits.

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NATURAL SCIENCES
NATURVETENSKAP

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