| Tartalom: |
http://real.mtak.hu/36256/ |
| Archívum: |
MTA Könyvtár |
| Gyűjtemény: |
Status = Published
Type = Article
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| Cím: |
Self-association-driven transition of the beta-peptidic H12 helix to the H18 helix
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| Létrehozó: |
Szolnoki, Éva Tünde
Hetényi, Anasztázia
Martinek, Tamás
Szakonyi, Zsolt
Fülöp, Ferenc
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| Kiadó: |
Royal Society of Chemistry Publishing
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| Dátum: |
2012
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| Téma: |
QD Chemistry / kémia
QD04 Organic chemistry / szerves kémia
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| Tartalmi leírás: |
Various patterns of foldameric oligomers formed by trans-ABHC ((1S,2S,3S, 5S)-2-amino-6,6-dimethylbicyclo-[3.3.1]heptane-3-carboxylic acid) and beta(3)-hSer residues were studied. NMR, ECD and molecular modelling demonstrated that octameric and nonameric sequences with multiple i-i+3 ABHC pair repulsions attain the beta-H18 helix in CD3OH. As a close relative of the alpha-helix, this helix type is stabilized by i-i+4 backbone H-bond interactions. The formation of the beta-H18 helix was found to be solvent-and concentration-dependent. Upon dilution, the beta-H18 -> beta-H12 helix transition was revealed by concentration-dependent ECD, DOSY-NMR and TEM measurements.
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| Nyelv: |
angol
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| Típus: |
Article
PeerReviewed
info:eu-repo/semantics/article
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| Formátum: |
text
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| Azonosító: |
Szolnoki, Éva Tünde and Hetényi, Anasztázia and Martinek, Tamás and Szakonyi, Zsolt and Fülöp, Ferenc (2012) Self-association-driven transition of the beta-peptidic H12 helix to the H18 helix. ORGANIC & BIOMOLECULAR CHEMISTRY, 10 (2). pp. 255-259. ISSN 1477-0520
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| Kapcsolat: |
MTMT:1842289; doi:10.1039/c1ob06627g
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