Protein Phosphorylation

Protein phosphorylation definition

Protein phosphorylation is a form of post-translational modification wherein a phosphate group (PO4) is reversibly attached to an amino group using a protein kinase. Since protein phosphorylation is a reversible process, a protein can return to its original confirmation and activity once the phosphate group is removed. This reverse reaction is called dephosphorylation, and it is catalyzed by enzymes called protein phosphatases.

Protein phosphorylation mechanism

So how exactly does protein phosphorylation work? Take a look at Figure 1 below.

Figure 1. In protein phosphorylation, a protein kinase transfers a phosphate group (PO4) from an ATP molecule and added to a protein. A protein phosphatase can reverse this process by removing the phosphate group.

The terminal phosphate group of an ATP molecule is removed and transferred to a polar R group of a protein—usually serine, threonine or tyrosine and sometimes histidine.

The polar amino acid contains a charged -OH group which is involved in a nucleophilic attack to the terminal phosphate group of ATP. The attack leads to the transfer of a phosphate group to the amino acid side chain.

Protein phosphorylation function

The addition of a phosphate group alters the proteins’ stability, function, subcellular activity and enzymatic activity. Because a phosphate group contains two negative charges, a protein that undergoes protein phosphorylation will have a change in charge, causing the ligand-binding of the protein to recruit positively-charged amino acid side chains.

The attachment of the phosphate group also results in the change in structure of binding, either making it more available for other proteins or blocking it from protein-binding interactions.

Protein phosphorylation plays a central role and is ubiquitous in different cellular processes. Phosphorylation is involved in cellular signaling that mediates cell proliferation, apoptosis, protein transport and degradation. In the following section, we will discuss the role of protein phosphorylation in cell signaling--particularly in signal transduction, in protein degradation, and in neurotransmission.

Protein phosphorylation example 1: cell signaling

Recall that cell signaling is the process in which a signaling molecule called a ligand attaches to a receptor protein inside or on the surface of a target cell, leading to a specific cellular function or response like cell proliferation and cell death.

While some ligands such as steroid hormones can permeate the hydrophobic interior of the plasma membrane, then bind to intracellular receptors in the cytoplasm and directly interact with DNA, other ligands such as hydrophilic amino acid-derived hormones cannot.

Ligands that cannot pass through the plasma membrane typically interact with cell-surface receptors that transmit the signal to other receptor proteins or messengers through a process called signal transduction, covered in the next section.

Protein phosphorylation example 2: signal transduction

To regulate signal transduction, phosphorylation usually acts as an on/off switch for a lot of cell-surface receptors and its downstream signaling: these proteins are activated by adding one or more phosphate groups.

Many signaling pathways involve multiple protein kinases that create a phosphorylation cascade. For the signal to be transmitted, protein kinases trigger phosphorylation one after another, each time causing shape change in the phosphorylated protein.

The shape change is caused by the interaction of the phosphate groups with the protein’s charged or polar amino acids. The change in shape modifies the protein’s function, thereby activating it. This provides the mechanism for “switching on” the signal transduction pathway.

Alongside protein kinases, protein phosphatases are also present in the phosphorylation cascade. Protein phosphatases dephosphorylate or remove phosphate groups from proteins, thereby inactivating them. This provides the mechanism for “switching off” the signal transduction pathway when the signal is gone. Dephosphorylation also makes protein kinases available for succeeding signals.

As such, the combination of phosphorylation and dephosphorylation acts as a molecular switch that activates or inactivates cellular activities as required. At any one time, the activity of a protein regulated by phosphorylation is determined by how many active kinase molecules and active phosphatase molecules a cell contains.

Protein phosphorylation example 3: degradation

The accumulation of proteins, especially misfolded proteins, is not favorable since this accumulation can lead to pathological diseases, such as Alzheimer's, ALS, and Huntingtons disease. To prevent damage, proteins need to be degraded by proteasomes. There are different mechanisms by which proteasomes degrade protein and protein phosphorylation is an essential part of these.

• Generally for protein degradation to occur, the activity of the enzyme ubiquitin ligase is turned on first by phosphorylating it. Once ubiquitin ligase is activated by phosphorylation, it can now form a multi-subunit ubiquitin ligase that can cause the degradation of proteins.

• Another way of degradation is for proteins to create a degradation signal. A degradation signal is created by phosphorylating a specific site on a protein. Once phosphorylated, a degradation signal that is typically hidden within a protein is revealed.

Protein phosphorylation example 4: neurotransmitters

Another example of protein phosphorylation is seen in our nervous systems. Phosphorylation is important to transfer information in neurotransmitters, the ligands responsible for carrying a signal from one neuron (or nerve cell) to a target cell in the body.

Enzymes that synthesize neurotransmitters need to be phosphorylated for synaptic transmission. In order to regulate this transmission, ion channels and receptors are phosphorylated. Upon phosphorylation, there is a change in conformation which switches the ion channel on and off.