4.3 Article

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

Journal

AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
Volume 17, Issue 3-4, Pages 101-104

Publisher

INFORMA HEALTHCARE
DOI: 10.3109/13506129.2010.526812

Keywords

Amyloidosis; amyloid protein; amyloid fibril; inclusion body

Funding

  1. NIA NIH HHS [R01 AG019259] Funding Source: Medline

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available