コンテンツへスキップ
Merck
  • Polyalanine-independent conformational conversion of nuclear poly(A)-binding protein 1 (PABPN1).

Polyalanine-independent conformational conversion of nuclear poly(A)-binding protein 1 (PABPN1).

The Journal of biological chemistry (2012-05-10)
Reno Winter, Uwe Kühn, Gerd Hause, Elisabeth Schwarz
要旨

Oculopharyngeal muscular dystrophy is a late-onset disease caused by an elongation of a natural 10-alanine segment within the N-terminal domain of the nuclear poly(A)-binding protein 1 (PABPN1) to maximally 17 alanines. The disease is characterized by intranuclear deposits consisting primarily of PABPN1. In previous studies, we could show that the N-terminal domain of PABPN1 forms amyloid-like fibrils. Here, we analyze fibril formation of full-length PABPN1. Unexpectedly, fibril formation was independent of the presence of the alanine segment. With regard to fibril formation kinetics and resistance against denaturants, fibrils formed by full-length PABPN1 had completely different properties from those formed by the N-terminal domain. Fourier transformed infrared spectroscopy and limited proteolysis showed that fibrillar PABPN1 has a structure that differs from native PABPN1. Circumstantial evidence is presented that the C-terminal domain is involved in fibril formation.