4.8 Article

The Supramolecular Chemistry of β-Sheets

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 135, 期 15, 页码 5477-5492

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ja3088407

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资金

  1. National Institutes of Health [1R01GM097562]
  2. NSF [CHE-1112188]
  3. Division Of Chemistry
  4. Direct For Mathematical & Physical Scien [1058825] Funding Source: National Science Foundation

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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.

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