The Supramolecular Chemistry of β-Sheets

被引:173
作者
Cheng, Pin-Nan [1 ]
Pham, Johnny D. [1 ]
Nowick, James S. [1 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
UNNATURAL AMINO-ACID; CRYSTAL-STRUCTURE; QUATERNARY STRUCTURE; AMYLOID FIBRILS; MOLECULAR RECOGNITION; ALZHEIMERS-DISEASE; TUMOR-SUPPRESSOR; CHEMICAL-MODELS; MET REPRESSOR; MUTANT P53;
D O I
10.1021/ja3088407
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Interactions among beta-sheets occur widely in protein quaternary structure, protein-protein interaction, and protein aggregation and are central in Alzheimer's and other amyloid-related diseases. This Perspective looks at the structural biology of these important yet under-appreciated interactions from a supramolecular chemist's point of view. Common themes in the supramolecular interactions of beta-sheets are identified and richly illustrated though examples from proteins, amyloids, and chemical model systems. beta-Sheets interact through edge-to-edge hydrogen bonding to form extended layers and through face-to-face hydrophobic or van der Waals interactions to form layered sandwich-like structures. Side chains from adjacent layers can fit together through simple hydrophobic contacts or can participate in complementary interdigitation or knob-hole interactions. The layers can be aligned, offset, or rotated. The right-handed twist of beta-sheets provides additional opportunities for stabilization of edge-to-edge contacts and rotated layered structures.
引用
收藏
页码:5477 / 5492
页数:16
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