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Search: (L773:0027 8424 OR L773:1091 6490) lar1:(su) pers:(Brännström Thomas) > Structural and kine...

Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mapping

Bergh, Johan, 1983- (author)
Umeå universitet,Institutionen för medicinsk biovetenskap
Zetterström, Per (author)
Umeå universitet,Institutionen för medicinsk biovetenskap
Andersen, Peter M. (author)
Umeå universitet,Klinisk neurovetenskap
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Brännström, Thomas (author)
Umeå universitet,Institutionen för medicinsk biovetenskap
Graffmo, Karin Sixtensdotter, 1960- (author)
Umeå universitet,Institutionen för medicinsk biovetenskap
Jonsson, P. Andreas (author)
Umeå universitet,Institutionen för medicinsk biovetenskap
Lang, Lisa (author)
Stockholms universitet,Institutionen för biokemi och biofysik
Danielsson, Jens (author)
Stockholms universitet,Institutionen för biokemi och biofysik
Oliveberg, Mikael (author)
Stockholms universitet,Institutionen för biokemi och biofysik
Marklund, Stefan (author)
Umeå universitet,Institutionen för medicinsk biovetenskap
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 (creator_code:org_t)
2015-03-23
2015
English.
In: Proceedings of the National Academy of Sciences of the United States of America. - : National Academy of Sciences. - 0027-8424 .- 1091-6490. ; 112:14, s. 4489-4494
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Despite considerable progress in uncovering the molecular details of protein aggregation in vitro, the cause and mechanism of protein-aggregation disease remain poorly understood. One reason is that the amount of pathological aggregates in neural tissue is exceedingly low, precluding examination by conventional approaches. We present here a method for determination of the structure and quantity of aggregates in small tissue samples, circumventing the above problem. The method is based on binary epitope mapping using anti-peptide antibodies. We assessed the usefulness and versatility of the method in mice modeling the neurodegenerative disease amyotrophic lateral sclerosis, which accumulate intracellular aggregates of superoxide dismutase-1. Two strains of aggregates were identified with different structural architectures, molecular properties, and growth kinetics. Both were different from superoxide dismutase-1 aggregates generated in vitro under a variety of conditions. The strains, which seem kinetically under fragmentation control, are associated with different disease progressions, complying with and adding detail to the growing evidence that seeding, infectivity, and strain dependence are unifying principles of neurodegenerative disease.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)
LANTBRUKSVETENSKAPER  -- Veterinärmedicin -- Medicinsk biovetenskap (hsv//swe)
AGRICULTURAL SCIENCES  -- Veterinary Science -- Medical Bioscience (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)

Keyword

protein aggregation
neurodegeneration
strain
amyotrophic lateral sclerosis
transgenic mice

Publication and Content Type

ref (subject category)
art (subject category)

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