Lipid polymorphism

In biophysics and colloidal chemistry, polymorphism is the ability of lipids to aggregate in a variety of ways, giving rise to structures of different shapes, known as "phases".

It forms an important part of current academic research in the fields of membrane biophysics (polymorphism), biochemistry (biological impact) and organic chemistry (synthesis).

The structural phase of the aggregation is influenced by the ratio of lipids present, temperature, hydration, pressure and ionic strength (and type).

The most common lipids that form this phase include phosphatidylethanolamine (PE), when it has unsaturated hydrocarbon chains.

The most common technique used to study phospholipid phase presence is phosphorus nuclear magnetic resonance (31P NMR).

Other techniques that are used and do offer definitive evidence of existence of lamellar and hexagonal phases include freeze-fracture electron microscopy, X-ray diffraction, differential scanning calorimetry (DSC), and deuterium nuclear magnetic resonance (2H NMR).

Additionally, negative staining transmission electron microscopy has been shown as a useful tool to study lipid bilayer phase behavior and polymorphism into lamellar phase, micellar, unilamellar liposome, and hexagonal aqueous-lipid structures, in aqueous dispersions of membrane lipids.

Cross Section view of the structures that can be formed by phospholipids in aqueous solutions
Inverted hexagonal H-II phase (H), inverted spherical micellar phase (M), lamellar liposomal phase (le) structures in cold-exposed aqueous dispersions of total lipid extract of spinach thylakoid membranes, studied by negative staining (2% phosphotungstic acid) transmission electron microscopy.