Selective disruption of protein aggregation by cyclodextrin dimers
β-Cyclodextrin (CD) dimers (n = 11) were synthesized and tested against eight enzymes, seven of which were dimeric or tetrameric, for inhibitor activity. Initial screening showed that only l-lactate dehydrogenase and citrate synthase were inhibited but only by two specific CD dimers in which two β-C...
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| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
2000
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC25779/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10805768/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.97.10.5050 |
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