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Supramolecular Bait to Trigger Non-Equilibrium Co-Assembly and Clearance of Aß42.
Wu, Te-Haw; Lai, Rai-Hua; Yao, Chun-Nien; Juang, Jyh-Lyh; Lin, Shu-Yi.
Afiliación
  • Wu TH; Institute of Biomedical Engineering and Nanomedicine, National Health Research Institutes (NHRI), Miaoli County, 35053, Taiwan.
  • Lai RH; Institute of Molecular and Genomic Medicine, NHRI, Taiwan.
  • Yao CN; Institute of Biomedical Engineering and Nanomedicine, National Health Research Institutes (NHRI), Miaoli County, 35053, Taiwan.
  • Juang JL; Institute of Molecular and Genomic Medicine, NHRI, Taiwan.
  • Lin SY; Institute of Biomedical Engineering and Nanomedicine, National Health Research Institutes (NHRI), Miaoli County, 35053, Taiwan.
Angew Chem Int Ed Engl ; 60(8): 4014-4017, 2021 02 19.
Article en En | MEDLINE | ID: mdl-33191624
ABSTRACT
In living systems, non-equilibrium states that control the assembly-disassembly of cellular components underlie the gradual complexification of life, whereas in nonliving systems, most molecules follow the laws of thermodynamic equilibrium to sustain dynamic consistency. Little is known about the roles of non-equilibrium states of interactions between supramolecules in living systems. Here, a non-equilibrium state of interaction between supramolecular lipopolysaccharide (LPS) and Aß42, an aggregate-prone protein that causes Alzheimer's disease (AD), was identified. Structurally, Aß42 presents a specific groove that is recognized by the amphiphilicity of LPS bait in a non-equilibrium manner. Functionally, the transient complex elicits a cellular response to clear extracellular Aß42 deposits in neuronal cells. Since the impaired clearance of toxic Aß42 deposits correlates with AD pathology, the non-equilibrium LPS and Aß42 could represent a useful target for developing AD therapeutics.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Lipopolisacáridos / Péptidos beta-Amiloides Idioma: En Revista: Angew Chem Int Ed Engl Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Lipopolisacáridos / Péptidos beta-Amiloides Idioma: En Revista: Angew Chem Int Ed Engl Año: 2021 Tipo del documento: Article