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A Capped Peptide of the Aggregation Prone NAC 71-82 Amino Acid Stretch of α-Synuclein Folds into Soluble β-Sheet Oligomers at Low and Elevated Peptide Concentrations

Näsström, Thomas (author)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB),Avancerade material,PPL;Linnaeus Ctr Biomat Chem, BMC,Linnaeus Univ, Phys Pharm Lab, Ctr Biomat Chem, SE-39231 Kalmar, Sweden.
Ådén, Jörgen, 1980- (author)
Umeå universitet,Kemiska institutionen,Umeå University, Sweden,Univ Umea, Dept Chem, SE-90187 Umea, Sweden.
Shibata, Fumina (author)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB),PPL;Linnaeus Ctr Biomat Chem, BMC,Linnaeus Univ, Phys Pharm Lab, Ctr Biomat Chem, SE-39231 Kalmar, Sweden.
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Andersson, Per-Ola (author)
Uppsala universitet,Tillämpad materialvetenskap
Karlsson, Björn C. G., Docent, 1977- (author)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB),Avancerade material,PPL;Linnaeus Ctr Biomat Chem, BMC,Linnaeus Univ, Phys Pharm Lab, Ctr Biomat Chem, SE-39231 Kalmar, Sweden.
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 (creator_code:org_t)
2020-02-27
2020
English.
In: International Journal of Molecular Sciences. - Basel, Switzerland : MDPI. - 1661-6596 .- 1422-0067. ; 21:5
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Although Lewy bodies and Lewy neurites are hallmarks of Parkinson's disease (PD) and dementia with Lewy bodies (DLB), misfolded α-synuclein oligomers are nowadays believed to be key for the development of these diseases. Attempts to target soluble misfolded species of the full-length protein have been limited so far, probably due to the fast aggregation kinetics and burial of aggregation prone segments in final cross-β-sheet fibrils. A previous characterisation study of fibrils prepared from a capped peptide of the non-amyloid β-component (NAC) 71-82 amino acid stretch of α-synuclein demonstrated an increased aggregation propensity resulting in a cross-β-structure that is also found in prion proteins. From this, it was suggested that capped NAC 71-82 peptide oligomers would provide interesting motifs with a capacity to regulate disease development. Here, we demonstrated, from a series of circular dichroism spectroscopic measurements and molecular dynamics simulations, the molecular-environment-sensitive behaviour of the capped NAC 71-82 peptide in a solution phase and the formation of β-sheet oligomeric structures in the supernatant of a fibrillisation mixture. These results highlighted the use of the capped NAC 71-82 peptide as a motif in the preparation of oligomeric β-sheet structures that potentially could be used in therapeutic strategies in the fight against progressive neurodegenerative disorders, such as PD and DLB.

Subject headings

NATURVETENSKAP  -- Biologi -- Biofysik (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biophysics (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Andra medicinska och farmaceutiska grundvetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Other Basic Medicine (hsv//eng)
NATURVETENSKAP  -- Biologi -- Strukturbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Structural Biology (hsv//eng)
NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

Keyword

Thioflavin T fluorescence
capped NAC 71–82 peptide
circular dichroism spectroscopy
molecular dynamics simulations
soluble β-sheet oligomers
α-synuclein
Biokemi

Publication and Content Type

ref (subject category)
art (subject category)

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