Chemical Biology of Prion Protein: Tools to Bridge the In Vitro/Vivo Interface

被引:3
|
作者
Seidel, Ralf [1 ]
Engelhard, Martin [1 ]
机构
[1] Max Planck Inst Mol Physiol, D-44227 Dortmund, Germany
来源
PRION PROTEINS | 2011年 / 305卷
关键词
Biophysical monitors; Chemical synthesis of proteins; Copper binding; Expressed protein ligation; Interaction of PrP with small molecules; AMYLOID FIBRILS; NEURODEGENERATIVE DISEASES; NMR STRUCTURES; BACTERIORHODOPSIN MUTANTS; INTRINSIC DISORDER; SYNTHETIC PEPTIDES; TRANSGENIC MICE; BETA OLIGOMERS; COPPER-BINDING; LIVING CELLS;
D O I
10.1007/128_2011_201
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Research on prion protein (PrP) and pathogenic prion has been very intensive because of its importance as model system for neurodegenerative diseases. One important aspect of this research has been the application of chemical biology tools. In this review we describe new developments like native chemical ligation (NCL) and expressed protein ligation (EPL) for the synthesis and semisynthesis of proteins in general and PrP in particular. These techniques allow the synthesis of designed tailor made analogs which can be used in conjunction with modern biophysical methods like fluorescence spectroscopy, solid state Nuclear Magnetic Resonance (ssNMR), and Electron Paramagnetic Resonance (EPR). Another aspect of prion research is concerned with the interaction of PrP with small organic molecules and metals. The results are critically reviewed and put into perspective of their implication for PrP function.
引用
收藏
页码:199 / 223
页数:25
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