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Reversible α-helix formation controlled by a hydrogen bond surrogate
Strategically placed covalent linkages have been shown to stabilize helical conformations in short peptide sequences. Here we report the synthesis of a stabilized α-helix that utilizes an internal disulfide linkage. Structural analysis indicates that the dynamic nature of the disulfide bridge allows...
Gorde:
| Egile Nagusiak: | , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2011
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3490425/ https://ncbi.nlm.nih.gov/pubmed/23144512 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tet.2011.12.068 |
| Etiketak: |
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