Amyloid fibril protein nomenclature: 2010 recommendations from the nomenclature committee of the International Society of Amyloidosis

被引:221
作者
Sipe, Jean D. [1 ]
Benson, Merrill D. [2 ]
Buxbaum, Joel N. [3 ]
Ikeda, Shu-ichi [4 ]
Merlini, Giampaolo [5 ]
Saraiva, Maria J. M. [6 ]
Westermark, Per [7 ]
机构
[1] Boston Univ, Sch Med, Dept Biochem Emerita, Boston, MA 02118 USA
[2] Indiana Univ Sch Med, Dept Pathol & Lab Med, Indianapolis, IN 46202 USA
[3] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA
[4] Shinshu Univ, Sch Med, Dept Neurol & Rheumatol, Matsumoto, Nagano 3908621, Japan
[5] Univ Pavia, Amyloid Res & Treatment Ctr, I-27100 Pavia, Italy
[6] Univ Porto, Amyloid Unit, Inst Mol & Cellular Biol, P-4100 Oporto, Portugal
[7] Uppsala Univ, Dept Genet & Pathol, S-75185 Uppsala, Sweden
来源
AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS | 2010年 / 17卷 / 3-4期
关键词
Amyloidosis; amyloid protein; amyloid fibril; inclusion body;
D O I
10.3109/13506129.2010.526812
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A system of amyloid fibril nomenclature based on the chemical identity of the amyloid fibril forming protein is recommended. This system has been in use for approximately 40 years, but current literature remains confused with clinical and histochemical designations used when the amyloid disease processes were poorly understood. To be designated an amyloid fibril protein, the protein must occur in tissue deposits and exhibit affinity for Congo red and green birefringence when viewed by polarisation microscopy. Furthermore, the protein must have been unambiguously characterised by protein sequence analysis ( DNA sequencing in the case of familial diseases). Current nomenclature lists of 27 human and nine animal fibril proteins are provided together with a list of eight inclusion bodies that exhibit some of the properties of amyloid fibrils.
引用
收藏
页码:101 / 104
页数:4
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