TY - JOUR
T1 - N-terminal sequence of prion protein is also intergrated into kuru plaques in patients with Gerstmann-Sträussler syndrome
AU - Kitamoto, Tetsuyuki
AU - Muramoto, Tamaki
AU - Hilbich, Caroline
AU - Beyreuther, Konrad
AU - Tateishi, Jun
N1 - Funding Information:
We thankK . Hatanakaan dM. Yonedaf or technicaals sistance, and B. Quinn for reviewingm anuscripTt.h is work was supported by grants( 024542450,1 570198f)r om the Ministryo f Education, Sciencea ndC ulture,t heM inistryo f Healtha ndW elfarea, ndthe Sciencea ndT echnologAyg encyJ,a pan.
Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1991/4/5
Y1 - 1991/4/5
N2 - Kuru plaques are one of the pathological hallmarks in Gerstmann-Sträussler syndrome, and are composed of prion protein (PrP). To elucidate whether N-terminal sequence of Prp is related to amygdaloid formation in vivo, we prepared antibody against synthetic N-terminal peptide (anti-PrP-N). Anti-PrP-N immunolabeled kuru plaques positively. Positive reactions were observed in the periphery of large kuru plaque cores, but not in the center. It is therefore postulated that one of the modification of Prp is N-terminal truncation.
AB - Kuru plaques are one of the pathological hallmarks in Gerstmann-Sträussler syndrome, and are composed of prion protein (PrP). To elucidate whether N-terminal sequence of Prp is related to amygdaloid formation in vivo, we prepared antibody against synthetic N-terminal peptide (anti-PrP-N). Anti-PrP-N immunolabeled kuru plaques positively. Positive reactions were observed in the periphery of large kuru plaque cores, but not in the center. It is therefore postulated that one of the modification of Prp is N-terminal truncation.
KW - Gerstmann-Sträussler syndrome
KW - Kuru plaque
KW - N-Terminal
KW - Prion protein
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U2 - 10.1016/0006-8993(91)91306-L
DO - 10.1016/0006-8993(91)91306-L
M3 - Article
C2 - 1677605
AN - SCOPUS:0025794115
SN - 0006-8993
VL - 545
SP - 319
EP - 321
JO - Molecular Brain Research
JF - Molecular Brain Research
IS - 1-2
ER -