𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Effect of acetylation and permethylation on the conformation and candidacidal activity of salivary histatin-5

✍ Scribed by Kalaiyarasi Ramalingam; Narayanan Ramasubbu; Michael J. Levine


Book ID
104632804
Publisher
Springer Netherlands
Year
1997
Tongue
English
Weight
608 KB
Volume
3
Category
Article
ISSN
1573-3149

No coin nor oath required. For personal study only.

✦ Synopsis


Salivary histatins provide the non-immune defense against oral pathogens such as Candida albicans. The structural requirements of histatin-5 for anticandida activity were examined with respect to its ability to adopt helical structures, its electrostatic interactions and the hydrogen-bonding potency of its basic residues. For this purpose, the lysine and/or histidine residues of histatin-5 were chemically modified by acetylation and permethylation. Acetylated histatin-5 retained its ability to adopt helical structures in 2,2,2-trifluoroethanol, but completely lost its ability to kill yeast cells. In contrast, permethylated histatin-5 shows very little tendency to adopt a helical structure, but retained significant anticandida activity. The results suggest that the candidacidal activity can arise even when the histatin does not have the ability to adopt helical structures. The candidacidal activity of the derivatives is discussed in terms of electrostatic interactions and hydrogen-bonding potency.


📜 SIMILAR VOLUMES


Conformational properties of α- and β-az
✍ Mark Froimowitz; P. Salva; G. J. Hite; G. Gianutsos; P. Suzdak; R. Heyman 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 695 KB

## Abstract Conformational energy calculations using the MM2 (molecular mechanics II) program are reported for diastereoisomeric α‐ and β‐azabicyclanes (3‐methyl‐9‐methoxy‐9‐phenyl‐3‐azabicyclo [3.3.1] nonanes) which are prototypical phenyl‐axial and phenyl‐equatorial opiates. After energy minimiza

Conformational studies on pyrimidine 5′-
✍ N. Yathindra; M. Sundaralingam 📂 Article 📅 1973 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 715 KB

## Abstract In continuation of our studies on the effect of the base and the phosphate groups on the glycosyl and the sugar‐phosphate backbone conformation, we have carried out semi‐empirical potential energy calculations on the common 5′‐ and 3′5′‐ribopyrimidine mono‐ and diphosphates by consideri