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Merck

Hydration of biological molecules: lipids versus nucleic acids.

Biopolymers (2002-09-05)
W Pohle, D R Gauger, U Dornberger, E Birch-Hirschfeld, C Selle, A Rupprecht, M Bohl
ABSTRACT

We used FTIR spectroscopy to comparatively study the hydration of films prepared from nucleic acids (DNA and double-stranded RNA) and lipids (phosphatidylcholines and phosphatidylethanolamines chosen as the most abundant ones) at room temperature by varying the ambient relative humidity in terms of solvent-induced structural changes. The nucleic acids and phospholipids both display examples of polymorphism on the one hand and structural conservatism on the other; even closely related representatives behave differently in this respect. DNA undergoes a hydration-driven A-B conformational transition, but RNA maintains an A-like structure independently of the water activity. Similarly, a main transition between the solid and liquid-crystalline phases can be induced lyotropically in certain phosphatidylcholines, while their phosphatidylethanolamine counterparts do not exhibit chain melting under the same conditions. A principal difference concerning the structural changes that occur in the studied biomolecules is given by the relevant water-substrate stoichiometries. These are rather high in DNA and often low in phospholipids, suggesting different mechanisms of action of the hydration water that appears to induce structural changes on global- and local-mode levels, respectively.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Polyadenylic acid · Polyuridylic acid potassium salt, free from low molecular weight nucleotides, lyophilized
Sigma-Aldrich
Polyadenylic acid-Polyuridylic acid sodium salt, double-stranded homopolymer