Actually, the cell membrane is a fluid. At room temperature, it has about a similar consistency as vegetable oil. Lipids, proteins, and sugars in the plasma membrane can diffuse unreservedly all through the cell membrane; they are basically skimming across its surface.
This is known as the liquid mosaic model, which was begat by S.J. Vocalist and G.L. Nicolson in 1972.
The extracellular segments of plasma membrane proteins are for the most part glycosylated. Moreover, the sugar segments of glycolipids are uncovered on the external substance of the plasma membrane.
Thusly, the outside of the cell is covered by a starch coat, known as the glycocalyx, shaped by the oligosaccharides of glycolipids and transmembrane glycoproteins.
Part of the job of the glycocalyx is to secure the cell surface. Also, the oligosaccharides of the glycocalyx fill in as markers for an assortment of cell-cell collaborations.
A very much considered illustration of these connections is the bond of white platelets (leukocytes) to the endothelial cells that line veins—a cycle that permits the leukocytes to leave the circulatory framework and intercede the incendiary reaction in harmed tissues.
The underlying advance in attachment among leukocytes and endothelial cells is interceded by a group of transmembrane proteins called selectins, which perceive explicit sugars on the cell surface.
Two individuals from the selectin family (E-selectin and P-selectin), communicated by endothelial cells and platelets, tie to explicit oligosaccharides communicated on the outside of leukocytes.
An alternate selectin (L-selectin) is communicated by leukocytes and perceives an oligosaccharide on the outside of endothelial cells.
The oligosaccharides uncovered on the cell surface subsequently give a bunch of markers that assist with recognizing the unmistakable cell sorts of multicellular creatures.