Identification of novel α-synuclein isoforms in human brain tissue by using an online nanoLC-ESI-FTICR-MS method.
Identification of novel α-synuclein isoforms in human brain tissue by using an online nanoLC-ESI-FTICR-MS method.
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通过使用在线纳米型-si-ftiCR-MS方法,鉴定人脑组织中新型α-突触核蛋白同工型。
DOI:
10.1007/s11064-011-0527-x
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发表时间:
2011-11
影响因子:
4.4
通讯作者:
Westman-Brinkmalm, Ann
中科院分区:
文献类型:
--
作者:
Ohrfelt, Annika;Zetterberg, Henrik;Andersson, Kerstin;Persson, Rita;Secic, Dzemila;Brinkmalm, Gunnar;Wallin, Anders;Mulugeta, Ezra;Francis, Paul T.;Vanmechelen, Eugeen;Aarsland, Dag;Ballard, Clive;Blennow, Kaj;Westman-Brinkmalm, Ann
Parkinson’s disease (PD) and Dementia with Lewy bodies (DLB) are neurodegenerative diseases that are characterized by intra-neuronal inclusions of Lewy bodies in distinct brain regions. These inclusions consist mainly of aggregated α-synuclein (α-syn) protein. The present study used immunoprecipitation combined with nanoflow liquid chromatography (LC) coupled to high resolution electrospray ionization Fourier transform ion cyclotron resonance tandem mass spectrometry (ESI-FTICR-MS/MS) to determine known and novel isoforms of α-syn in brain tissue homogenates. N-terminally acetylated full-length α-syn (Ac-α-syn1–140) and two N-terminally acetylated C-terminally truncated forms of α-syn (Ac-α-syn1–139 and Ac-α-syn1–103) were found. The different forms of α-syn were further studied by Western blotting in brain tissue homogenates from the temporal cortex Brodmann area 36 (BA36) and the dorsolateral prefrontal cortex BA9 derived from controls, patients with DLB and PD with dementia (PDD). Quantification of α-syn in each brain tissue fraction was performed using a novel enzyme-linked immunosorbent assay (ELISA).
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影响因子:
4.7
作者:
Campbell, BCV;McLean, CA;Li, QX
通讯作者:
Li, QX
影响因子:
4.4
作者:
CAMPION, D;MARTIN, C;FREBOURG, T
通讯作者:
FREBOURG, T
影响因子:
9.9
作者:
Ballard, C.;Ziabreva, I.;Aarsland, D.
通讯作者:
Aarsland, D.
影响因子:
4.8
作者:
Kubo, S;Nemani, VM;Fortin, DL
通讯作者:
Fortin, DL
影响因子:
14.5
作者:
Hong, Zhen;Shi, Min;Zhang, Jing
通讯作者:
Zhang, Jing