1. Mechanism

2. Mathematical definition

3. Implications and Uses in Biological Systems
     Involvement in Cancer Mechanisms    Importance in Cell and Organelle Membranes    Presence in the Cerebellar Granule Layer  

4. References

While uncompetitive inhibition requires that an enzyme-substrate complex must be formed, non-competitive inhibition can occur with or without the substrate present.

Uncompetitive inhibition is distinguished from competitive inhibition by two observations: first uncompetitive inhibition cannot be reversed by increasing [S] and second, as shown, the Lineweaver–Burk plot yields parallel rather than intersecting lines. This behavior is found in the inhibition of acetylcholinesterase by tertiary amines (R₃N). Such compounds bind to the enzyme in its various forms, but the acyl-intermediate-amine complex cannot break down into enzyme plus product.^[2]

Mechanism

Uncompetitive inhibition is unique in that the inhibitor binds to the enzyme-substrate complex. This could imply that the binding site for the inhibitor is accessible only after the enzyme has bound to its substrate.^[3]

As inhibitor binds, the amount of ES complex is reduced. This reduction in the effective concentration of the ES complex can be explained by the fact that having the inhibitor bound to the ES complex essentially converts it to ESI complex, which is considered a separate complex altogether. This reduction in ES complex decreases the maximum enzyme activity (V_max), as it takes longer for the substrate or product to leave the active site. The reduction in K_m - the substrate concentration at which the enzyme can operate at half of its maximal velocity, often used to approximate an enzyme's affinity for a substrate - can also be linked back to the decrease in ES complex. Le Chatelier's principle opposes this decrease and attempts to make up for the loss of ES, so more free enzyme is converted to the ES form, and the amount of ES increases overall. An increase in ES generally indicates that the enzyme has a high degree of affinity for its substrate. K_m decreases as affinity for a substrate increases, though it is not a perfect predictor of affinity since it accounts for other factors as well; regardless, this increase in affinity will be accompanied by a decrease in K_m.^[4]

In general, uncompetitive inhibition works best when substrate concentration is high. An uncompetitive inhibitor need not resemble the substrate of the reaction it is inhibiting.

Mathematical definition

The Lineweaver–Burk equation states that:

Where v is the initial reaction velocity, K_m is the Michaelis–Menten constant, V_max is the maximum reaction velocity, and [S] is the concentration of the substrate.^[5]

The Lineweaver–Burk plot for an uncompetitive inhibitor produces a line parallel to the original enzyme-substrate plot, but with a higher y-intercept, due to the presence of an inhibition term :

Where [I] is the concentration of the inhibitor and K_i is an inhibition constant characteristic of the inhibitor.^[6][7]

The Michaelis-Menten equation is altered to:

where

and

As described by the equation above, at high concentrations of substrate, V₀ approaches V_max/α'. Thus, an uncompetitive inhibitor lowers the measured V_max. Apparent K_m also decreases, because [S] required to reach one-half V_max decreases by the factor α'.^[8] It is important to note that V_max and K_m decrease at the same rate as a result of the inhibitor.^[3] This is apparent when viewing a Lineweaver-Burk plot of uncompetitive enzyme inhibition: the ratio between V and K_m remains the same with or without an inhibitor present.

Implications and Uses in Biological Systems

The unique traits of uncompetitive inhibition lead to a variety of implications for the inhibition's effects within biological and biochemical systems. Uncompetitive inhibition is present within biological systems in a number of ways. In fact, it often becomes clear that the traits of inhibition specific to uncompetitive inhibitors, such as their tendency to act at their best at high concentrations of substrate, are essential to some important bodily functions operating properly.^[9]

Involvement in Cancer Mechanisms

Uncompetitive mechanisms are involved with certain types of cancer. Human alkaline phosphatases such as CGAP have been found to be over-expressed in certain types of cancers, and those phosphotases often operate via uncompetitive inhibition. It has also been found that a number of the genes that code for human alkaline phosphatases (TSAPs) are inhibited uncompetitively by amino acids such as Leucine and Phenylalanine.^[10] Studies of the involved amino acid residues have been undertaken in attempts to regulate alkaline phosphatase activity and learn more about said activity's relevance to cancer.^[11]

Additionally, uncompetitive inhibition works alongside TP53 to help repress the activity of cancer cells and prevent tumorigenesis in certain forms of the illness, as it inhibits G6PD (glucose-6-phosphate dehydrogenase, an enzyme primarily involved in certain metabolic pathways). One of the side roles G6PD is responsible for is helping to regulate is the control of reactive oxygen levels, as reactive oxygen species must be kept at appropriate levels to allow cells to survive. When G6PD's substrate concentration is high, uncompetitive inhibition of the enzyme becomes far more effective.^[12] As substrate concentration increases, the amount of ES complex increases as well, and with more ES complex to bind, uncompetitive inhibitors become far more active. This inhibition works such that the higher the concentration of substrate is in the system initially, the harder it is to reach the maximum velocity of the reaction. At low initial substrate concentrations, increasing the concentration of substrate is sometimes enough to entirely or even fully restore the enzyme's function, but as soon as initial concentration increases past a certain point, reaching the maximal enzyme velocity is all but impossible.^[13] It should be noted that this extreme sensitivity to substrate concentration within the cancer mechanism implicates uncompetitive inhibition rather than mixed inhibition, which displays similar traits but is often less sensitive to substrate concentration due to some inhibitor binding to free enzymes regardless of the substrate's presence.^[13] As such, the extreme strength of uncompetitive inhibitors at high substrate concentrations and the overall sensitivity to substrate amount indicates that only uncompetitive inhibition can make this type of process possible.

Importance in Cell and Organelle Membranes

Although this form of inhibition is present in various diseases within biological systems, it does not necessarily only relate to pathologies. It can be involved in typical bodily functions. For example, active sites capable of uncompetitive inhibition appear to be present in membranes, as removing lipids from cell membranes and making active sites more accessible through conformational changes has been shown to invoke elements resembling the effects of uncompetitive inhibition (i.e. both K_M and V_Max decrease). In mitochondrial membrane lipids specifically, removing lipids decreases the alpha-helix content in mitochondria and leads to changes in ATPase resembling uncompetitive inhibition.^[14]

This presence of uncompetitive enzymes in membranes has also been supported in a number of other studies. A type of protein called an Arf protein involved in regulating membrane activity was being studied, and it was found that an inhibitor called BFA trapped one of Arf's intermediates via uncompetitive inhibition. This made it clear that this type of inhibition exists within various types of cells and organelles as opposed to just in pathological cells. In fact, BFA was found to relate to the activity of the Golgi apparatus and its role in regulating movement across the cell membrane.^[15]

Presence in the Cerebellar Granule Layer

Uncompetitive inhibition can play roles in various other parts of the body as well. It is part of the mechanism by which NMDA (N-methyl-D-aspartate) glutamate receptors are inhibited in the brain, for example. Specifically, this type of inhibition impacts the granule cells that make up a layer of the cerebellum. These cells have the aforementioned NMDA receptors, and the activity of said receptors typically increases as ethanol is consumed. This often leads to withdrawal symptoms if said ethanol is removed. Various uncompetitive blockers act as antagonists at the receptors and modify the process, with one example being an inhibitor called memantine.^[16] In fact, in similar cases (involving over-expression of NMDA, though not necessarily via ethanol), it has been shown that uncompetitive inhibition helps in nullifying the over-expression due to its particular properties. Since uncompetitive inhibitors block high concentrations of substrates very efficiently, their traits alongside the innate characteristics of the receptors themselves lead to very effective blocking of NMDA channels when they are excessively open due to massive amounts of NMDA agonists.^[17]

References

• Georg Heibl
• Georg Heinrich Friedrich Hitzig
• Georg Heinrich Sieveking
• Georg Hellat
• Georghe muresan
• Georg henrik von wright
• Georg Hermann Alexander Ochs
• Georg Hermann Nicolai
• Georg Hermann Quincke
• Georg Hettich
• Georg Heym
• Georghe Zamphir
• Georghios Pikis
• Georghi Todorov
• Georg Hoberg
• Georg Hochfilzer
• Georg Hoeberg
• Georg Hoefnagel
• Georg Hoffmann
• Georg Holm
• Georg H. Schnell
• Georg Huth
• Georg Hólm
• Georg Høberg
• Georg Høeberg