1NMJ

The Solution Structure of Rat Ab-(1-28) and its Interaction with Zinc: Insights into the Scarity of Amyloid Deposition in Aged Rat Brain

Summary for 1NMJ

• Entry DOI: 10.2210/pdb1nmj/pdb
• Related: 1AMB 1AMC 1BJB 1BJC
• NMR Information: BMRB: 5735
• Descriptor: amyloid beta-peptide from Alzheimer's disease amyloid A4 protein homolog (1 entity in total)
• Functional Keywords: glycoprotein, amyloid, membrane protein
• Biological source: Rattus norvegicus (Norway rat)
• Cellular location: Membrane; Single-pass type I membrane protein: P08592
• Total number of polymer chains: 1
• Total formula weight: 3171.41

Authors

Huang, J.,Yao, Y.,Tang, W.X. (deposition date: 2003-01-10, release date: 2003-01-28, Last modification date: 2024-05-29)

Primary citation

Huang, J.,Yao, Y.,Lin, J.,Ye, Y.H.,Sun, W.Y.,Tang, W.X.
The solution structure of rat Abeta-(1-28) and its interaction with zinc ion: insights into the scarcity of amyloid deposition in aged rat brain
J.Biol.Inorg.Chem., 9:627-635, 2004

PubMed Abstract: The amyloid beta-peptide (Abeta) is a major component of insoluble amyloid deposits in Alzheimer's disease, and the ability of the beta-peptide to exist in different conformations is dependent on residues 1-28 [beta-(1-28)]. However, different from humans, no Abeta amyloid deposition has been found in aged rats' brains. Studying the three-dimensional solution structure of rat Abeta-(1-28) and the binding circumstance of Zn(2+) is beneficial to a clear understanding of the potential role of Zn(2+) in Alzheimer-associated neuropathogenesis and to suggest why there is no amyloid deposition in aged rats' brains. Here we used nuclear magnetic resonance (NMR) spectroscopy to determine the solution structure of rat Abeta-(1-28) and the binding constant of Zn(2+) to rat Abeta-(1-28). Our results suggest that (1) the three-dimensional solution structure of rat Abeta-(1-28) is more stable than that of human Abeta-(1-28) in DMSO- d(6) and that a helical region from Glu16 to Val24 exists in the rat Abeta-(1-28); (2) the affinity of Zn(2+) for rat Abeta-(1-28) is lower than that for human Abeta-(1-28) and the NMR data suggest that Arg13, His6, and His14 residues provide the primary binding sites for Zn(2+); and (3) the proper binding of Zn(2+) to rat Abeta-(1-28) can induce the peptide to change to a more stable conformation.

PubMed: 15160315
DOI: 10.1007/s00775-004-0556-x

Experimental method

SOLUTION NMR