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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Abstract
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.
Item Type: | Article |
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Uncontrolled Keywords: | CIRCULAR-DICHROISM; SECONDARY STRUCTURE; QUATERNARY STRUCTURE; AMPHIPATHIC PEPTIDES; MEMBRANE ENVIRONMENT; HETEROGENEOUS BACKBONES; STRUCTURAL-CHARACTERIZATION; SIDE-CHAINS; ACID OLIGOMERS; ALPHA/BETA-PEPTIDES |
Subjects: | Q Science / természettudomány > QD Chemistry / kémia Q Science / természettudomány > QD Chemistry / kémia > QD04 Organic chemistry / szerves kémia |
SWORD Depositor: | MTMT SWORD |
Depositing User: | MTMT SWORD |
Date Deposited: | 10 Jun 2016 13:27 |
Last Modified: | 10 Jun 2016 13:27 |
URI: | http://real.mtak.hu/id/eprint/36256 |
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