1LDS
Crystal Structure of monomeric human beta-2-microglobulin
1LDS の概要
| エントリーDOI | 10.2210/pdb1lds/pdb |
| 関連するPDBエントリー | 1DUZ |
| 分子名称 | beta-2-microglobulin, SODIUM ION (3 entities in total) |
| 機能のキーワード | immunoglobulin constant domain, immune system |
| 由来する生物種 | Homo sapiens (human) |
| 細胞内の位置 | Secreted: P61769 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 11902.35 |
| 構造登録者 | Trinh, C.H.,Smith, D.P.,Kalverda, A.P.,Phillips, S.E.V.,Radford, S.E. (登録日: 2002-04-09, 公開日: 2002-07-31, 最終更新日: 2024-11-20) |
| 主引用文献 | Trinh, C.H.,Smith, D.P.,Kalverda, A.P.,Phillips, S.E.,Radford, S.E. Crystal structure of monomeric human beta-2-microglobulin reveals clues to its amyloidogenic properties. Proc.Natl.Acad.Sci.USA, 99:9771-9776, 2002 Cited by PubMed Abstract: Dissociation of human beta-2-microglobulin (beta(2)m) from the heavy chain of the class I HLA complex is a critical first step in the formation of amyloid fibrils from this protein. As a consequence of renal failure, the concentration of circulating monomeric beta(2)m increases, ultimately leading to deposition of the protein into amyloid fibrils and development of the disorder, dialysis-related amyloidosis. Here we present the crystal structure of a monomeric form of human beta(2)m determined at 1.8-A resolution that reveals remarkable structural changes relative to the HLA-bound protein. These involve the restructuring of a beta bulge that separates two short beta strands to form a new six-residue beta strand at one edge of this beta sandwich protein. These structural changes remove key features proposed to have evolved to protect beta sheet proteins from aggregation [Richardson, J. & Richardson, D. (2002) Proc. Natl. Acad. Sci. USA 99, 2754-2759] and replaces them with an aggregation-competent surface. In combination with solution studies using (1)H NMR, we show that the crystal structure presented here represents a rare species in solution that could provide important clues about the mechanism of amyloid formation from the normally highly soluble native protein. PubMed: 12119416DOI: 10.1073/pnas.152337399 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.8 Å) |
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