Why is hydrophobic interaction a bad term




















The mixing of fat and water is a good example of this particular interaction. However, this is not the case. The behavior of a fat droplet in water has more to do with the enthalpy and entropy of the reaction than its intermolecular forces.

American chemist Walter Kauzmann discovered that nonpolar substances like fat molecules tend to clump up together rather than distributing itself in a water medium, because this allow the fat molecules to have minimal contact with water. The image above indicates that when the hydrophobes come together, they will have less contact with water. They interact with a total of 16 water molecules before they come together and only 10 atoms after they interact.

When a hydrophobe is dropped in an aqueous medium, hydrogen bonds between water molecules will be broken to make room for the hydrophobe; however, water molecules do not react with hydrophobe.

This is considered an endothermic reaction, because when bonds are broken heat is put into the system. Fats are triglyceride esters, composed of three fatty acids esterified to a single glycerol molecules. An ester linkage is a covalent bond between a carboxylic acid and an alcohol. Soap micelles mobilize fats and other hydrophobic substances by dissolving them in the interior of the micelle.

Because the micelles are suspended in water, the fat is mobilized from the surface of the object being cleaned. Detergents are stronger cleaning agents than are soaps, mostly because their hydrophilic component is more highly charged than the fatty acid component of a soap. For example, sodium dodecyl sulfate is a component of commercially available hair shampoos. It is a powerful enough detergent that it is often used experimentally to disrupt the hydrophobic interactions that hold membranes together or that contribute to protein shape.

When phosphatidylcholine is suspended in water, the molecules associate by the hydrophobic effect, with the charged portion facing the solvent and the fatty acid side chains associating with each other.

The model compound studies predict that the hydrophobic effect of exposing one buried methylene group to bulk water is 0. The site directed mutagenesis studies yielded a larger number with greater statistical variation: the average hydrophobic effect estimated by SDM for a buried methylene group is about 1. However, when the SDM results for methylene were plotted against the size of the cavity created by the residue substitution, and extrapolated to zero, the result at zero cavity size is 0.

In the SDM studies, cavities created by residue substitution have an additional destabilizing effect: the loss of favourable VDWs interactions as compared to the wild-type. Thus, the "hydrophobic effect" measured by SDM includes both an entropic component due to solvent ordering and a primarily enthalpic component due to loss of VDWs contacts within the protein. This is smaller than expected c.

Click here for a gif showing the cavity and links to the structures. Hydrophilic substances are water-loving molecules that are polar in nature. They are easily soluble in water and examples of such substances are sugar, salt, starch, and cellulose.

The extent to which the surface of hydrophilic molecules attracts water molecules is called hydrophilicity. On the other side, hydrophobic as explained earlier is water repellent and thus due to their non-polar nature, is not miscible in water. It is often seen that the terms such as hydrophobic and lipophilic come together but the two words demonstrate very different concepts.

Hydrophobic substances are water repellent substances while lipophilic are fat-loving molecules. It can be seen in various literature that most of the hydrophobic substances are lipophilic in nature except silicones and fluorocarbons. The relations between water and hydrophobes are well described under the umbrella of hydrophobic interactions. The relative mixing of water with fat is a very handy example of such interactions. Moreover, heat has to be given to the system to break the tight hydrogen bond, and thus the reaction is endothermic.

New hydrogen bonds form that shape into an ice-like cage structure known as a clathrate cage around the surface of the hydrophobe. This orientation of the clathrate cage makes the system more structured and the total entropy a measure of disorderliness of the system is decreased.

Furthermore, the strength of the hydrophobic interactions depends on the temperature, the number of carbon atoms present in the hydrophobe, and the shape and dimensions of the hydrophobic molecule [3]. The hydrophobic interactions are very important in protein folding making it stable and biologically active. The interactions will give a chance to protein to reduce its surface and to avoid the undesired interactions with the water molecule.

Similarly, the phospholipid bilayer membranes present in every cell in the human body also depend on the hydrophobic interactions for their survival and optimum functioning. There are many advantages to employing hydrophobic substances for domestic and industrial applications. Hydrophobes are usually low-energy surface materials that resist wetting and have improved corrosion resistance.

Such substances are used for improved moisture detection instrumentations and to prevent moisture contamination in heat trace tubing and analytical sample transfer systems. Moreover, hydrophobes are also employed in HPLC medical diagnostics improved separation and corrosion resistance systems.

Similarly, the hydrophobic surfaces are used in anti-biofouling paints for boots, refining of metals, stain-resistant textiles, the separation of oil and water, in the textile industry, and the manufacture of fire retardant and waterproof clothes [4].

The hydrophobicity can be measured by various analytical techniques such as hydrophobic interaction chromatography , contact angle measurement , and rose bengal measurement. It is worth mentioning here that the identification of groups present in the particle is very important while measuring hydrophobicity. The most frequent method that has been used to calculate the hydrophobicity of the surface is via the calculation of contact angle in between the droplets of water and the surface itself.

A contact angle of more than 90 degrees is usually maintained by the water droplet flowing over a hydrophobic surface and retains a spherical shape. Moreover, the superhydrophobic materials possess a relatively larger contact angle of above degrees. Upon contact with the hydrophilic surfaces, the droplets of water spread out far and the contact angle is generally small and is less than 90 degrees.



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