Ligands and receptors are both usually proteins. Since proteins can fold into a wide variety of shapes, the receptor-ligand interaction is very specific. In some cases, certain receptors will bind two ligands that are similar in structure. For example, hemoglobin binds to both  and , but binds  with much higher affinity. Ligands bind receptors using only weak bonds (hydrogen bonds and Van der Waals forces). Depending on the nature of the ligand (whether it can cross the lipid bilayer or not), its receptor may be either on the cell's surface, floating in the cytoplasm, or on the nuclear membrane.

In biochemistry, ligands are any substance that forms a complex with a biomolecule to serve a biological purpose. The four primary types of ligands have their functional state determined by their three-dimensional chemical conformation. Tracers in the body often take the form of radioligands, but are not ligands themselves.

Chemotaxis refers to the movement of an organism in response to a chemical stimulus. Single or multicellular organisms may direct their movements according to certain chemicals in their environment. This is important because these organisms need to find food, flee from harmful substances, and chemotaxis also aids in development. Positive chemotaxis is movement towards a higher concentration of the chemical, whereas negative chemotaxis is movement away from the chemical.  

Glycolysis (the process of breaking down glucose) takes place in the cytoplasm, or cytosol—the aqueous portion of the cytoplasm. It is in the cytoplasm where the enzymes required for glycolysis are found.

The citric acid cycle takes place in the mitochondrial matrix, and the electron transport chain takes place along the inner mitochondrial membrane in order to pump protons into the intermembrane space.

The addition and removal of phosphate groups can serve critical functions in the regulation of protein activity. The binding or uncoupling of phosphate groups frequently serves to activate or deactivate proteins.

A kinase is an enzyme that phosphorylates—or adds a phosphate group to—its ligand.

A phosphatase removes a phosphate group from its ligand.

Several different types of proteins can change the structure of a ligand, such as isomerases, and ubiquitin ligases add ubiquitin to their ligands.

The addition and removal of phosphate groups can serve critical functions in the regulation of protein activity. The binding or uncoupling of phosphate groups frequently serves to activate or deactivate proteins.

A phosphatase removes a phosphate group from its ligand.

A kinase is an enzyme that phosphorylates—or adds a phosphate group to—its ligand.

Several different types of proteins can change the structure of a ligand, such as isomerases, and ubiquitin ligases add ubiquitin to their ligands.

Ubiquitin ligases add ubiquitin to their ligands. The addition of ubiquitin acts as a signal that a protein has become ineffective and is ready for degradation. When multiple ubiquitin residues have been added to a protein molecule, it is transported to the lysosome in the cell to be digested.

A phosphatase removes a phosphate group from its ligand.

A kinase is an enzyme that phosphorylates—or adds a phosphate group to—its ligand.

The addition and removal of phosphate groups can serve critical functions in the regulation of protein activity. The binding or uncoupling of phosphate groups frequently serves to activate or deactivate proteins.

Several different types of proteins can change the structure of a ligand, such as isomerases.

A cell must exchange molecules and ions with its surroundings.  This process is controlled by the selective permeability of the plasma membrane.  Passive transport requires no energy from the cell; molecules like water can diffuse into and out of the cell through the phospholipid bilayer freely by way of osmosis.  Other molecules and ions, like sodium, are actively transported across the phospholipid bilayer.  This requires ATP created by the cell.  Active transport moves solutes against their concentration gradients, which is why it requires energy. 

Tonofibrils are groups of keratin tonofilaments (intermediate filaments) most commonly found in the epithelial tissues, not endocrine tissues, and which play an important structural role in cell makeup.

The primary ability of secondary messengers is their ability to leave the cell membrane and travel through the phospholipid bilayer by being selectively hydrophilic or -phobic, allowing egress. This enables, for example, a cascade effect that greatly amplifies the strength of the original primary messenger signal.