One of the most surprising characteristics of biological membranes is the fact that both the lipid and the protein molecules, like molecules in any viscous liquid, are constantly in motion. Indeed, the membrane can be considered a two-dimensional liquid in which the protein components ride like boats. However, the lipid molecules in the bilayer must always be oriented with their polar ends at the surface and their nonpolar parts in the central region of the bilayer. The bilayer structure thus has the molecular orientation of a crystal and the fluidity of a liquid. In this liquid-crystalline state, thermal energy causes both lipid and protein molecules to diffuse laterally and also to rotate about an axis perpendicular to the membrane plane. In addition, the lipids occasionally flip from one face of the membrane bilayer to the other and attach and detach from the surface of the bilayer at very slow but measurable rates. Although these latter motions are forbidden to intrinsic proteins, both lipids and proteins can exhibit limited bobbing motions. Within this seemingly random, dynamic mixture of components, however, there is considerable order in the plane of the membrane. This order takes the form of a “fluid mosaic” of molecular association complexes of both lipids and proteins in the membrane plane. The plane of the biological membrane is thus compartmentalized by domain structures much as the three-dimensional space of the cell is compartmentalized by the membranes themselves. The domain mosaics run in size from tens of nanometres (billionths of a metre) to micrometres (millionths of a metre) and are stable over time intervals of nanoseconds to minutes. In addition to this in-plane domain structure, the two lipid monolayers making up the membrane bilayer frequently have different compositions. This asymmetry, combined with the fact that intrinsic membrane proteins do not rotate about an axis in the membrane plane, makes the two halves of the bilayer into separate domains.

An interesting class of proteins is attached to biological membranes by a lipid that is chemically linked to the protein. Many of these proteins are involved in intra- and intercellular signaling. In some cases defects in their structure render the cells cancerous, presumably because growth-limiting signals are blocked by the structural error.

Steroid hormones

Lipid hormones invoke changes in gene expression; that is, their action is to turn on or off the instructions issued by deoxyribonucleic acid (DNA) to produce proteins that regulate the biosynthesis of other important proteins. Steroids are carried in the circulation bound singly to specific carrier proteins that target them to the cells in particular organs. After permeating the external membranes of these cells, the steroid interacts with a specific carrier protein in the cytoplasm. This soluble complex migrates into the cell nucleus, where it interacts with the DNA to activate or repress transcription, the first step in protein biosynthesis.

All five major classes of steroid hormones produced from cholesterol contain the characteristic five rings of carbon atoms of the parent molecule. Progestins are a group of steroids that regulate events during pregnancy and are the precursors of the other steroid hormones. The glucocorticoids, cortisol, and corticosterones promote the biosynthesis of glucose and act to suppress inflammation. The mineralocorticoids regulate ion balances between the interior and the exterior of the cell. Androgens regulate male sexual characteristics, and estrogens perform an analogous function in females. The target organs for these hormones are listed in the table.

Eicosanoids

Three types of locally acting signaling molecules are derived biosynthetically from C₂₀ polyunsaturated fatty acids, principally arachidonic acid. Twenty-carbon fatty acids are all known collectively as eicosanoic acids. The three chemically similar classes are prostaglandins, thromboxanes, and leukotrienes. The eicosanoids interact with specific cell surface receptors to produce a variety of different effects on different tissues, but generally they cause inflammatory responses and changes in blood pressure, and they also affect the clotting of blood. Little is known about how these effects are produced within the cells of target tissues. However, it is known that aspirin and other anti-inflammatory drugs inhibit either an enzyme in the biosynthesis pathway or the eicosanoid receptor on the cell surface.