I. Collagen-like polypeptides. II. Helix-turn-helix peptides and turn mimetics.
MetadataShow full item record
The conformationally locked alkene isosteres Fmoc-Gly-Î¨[(E)CH=C]-Pro-Hyp(tBu)-OH and Fmoc-Pro-Î¨[(E)CH=C]-Pro-OH were designed and synthesized. The synthesis of the Gly-Pro isostere had no stereo-control, and the two diastereomers of the tripeptide isostere Fmoc-Gly-Î¨[(E)CH=C]-Pro-Hyp(tBu)-OBn were separated by normal phase HPLC. Although the stereoselectivity of the asymmetric reduction was not good for the Pro-Pro isostere, the resulting diastereomers was separable by flash chromatography, and the absolute stereochemistry of the two diastereomers was determined by Mosherâ s method. The Gly-Pro alkenyl peptides, and their control peptide Ac-(Gly-Pro-Hyp)8-Gly-Gly-Tyr-NH2 were synthesized and purified. All three peptides showed a maximum around 225 nm and a minimum close to 200 nm in the CD spectra, which indicated the formation of PPII helixes. The Tm value of the control peptide was determined to be 50.0 Â°C. The peptide with Gly-Î¨[(E)CH=C]-L-Pro-Hyp as the guest triplet formed a stable triple helix with a Tm value of 28.3 Â°C. The peptide with Gly-Î¨[(E)CH=C]-D-Pro-Hyp as the guest triplet showed a linear decrease in the ellipticity with increasing temperature, which indicated that no triple helix was formed.
The Pro-Pro alkenyl peptide and its control peptide H-(Pro-Pro-Gly)10-OH were synthesized and purified. The Tm value of control peptide was determined to be 31.6 Â°C by extrapolation to 0 M TMAO in PBS buffer, which was very close to the measured value of 31.5 Â°C. The Pro-Pro alkenyl peptide began to show a maximum around 225 nm in the CD spectra when the concentration of TMAO was higher than 2.5 M. After extrapolation to 0 M TMAO, the Tm value was determined to be â 22.0 Â°C. These results indicate that the backbone inter-chain hydrogen bond is one of the major forces in stabilizing the collagen triple helix, while cis-trans isomerization has limited contribution. The intrinsic properties of the amide bond may have huge influence on the stability of the collagen triple helix.
The helix-turn-helix motif is an important tertiary structure in DNA-binding proteins. Stepwise modifications of the Antennapedia HTH peptide (27-55) were performed to improve the helicity and stability. The peptide with more side-chain ion-pairs was over 4 times more helical than the native Antp peptide, while the Ala-based peptide was over 9 times more helical than the native peptide.
A 12-membered ring, Fmoc-protected HTH-turn mimic was designed and synthesized, and was ready for solid phase peptide synthesis. The solubility of the cyclic peptide was very poor, and the purification of the final product was very difficult. The solubility problem might also affect solid phase peptide synthesis in the future.
- Doctoral Dissertations 
Showing items related by title, author, creator and subject.
Transcriptional Regulation of Melanocortin 4 Receptor by Nescient Helix-Loop-Helix-2 and its Implications in Peripheral Energy Homeostasis Wankhade, Umesh D. (Virginia Tech, 2010-05-13)Mutations in the melanocortin 4 receptor (MC4R) are the most frequent cause of monogenetic forms of human obesity. Despite its importance, the MC4R signaling pathways and transcriptional regulation that underly the ...
Nescient helix-loop-helix 2 interacts with signal transducer and activator of transcription 3 to regulate transcription of prohormone convertase 1/3 Fox, D. L.; Good, D. J. (Endocrine Society, 2008-06)Mechanisms controlling body weight involve gene regulation through the activation of signal transduction pathways. The Janus kinase/signal transducer and activator of transcription (STAT) signal transduction pathway is the ...
Part 1 Synthesis of a potent histone deacetylase inhibitor Part 2 Studies towards a stabilized helix-turn-helix peptide Liu, Tao (Virginia Tech, 2007-01-15)The first part of this work describes the synthesis of a new histone deacetylase (HDAC) inhibitor (HDI). HDAC enzymes modify core histones, influence nucleosome structure and change gene transcription by removing the acetyl ...