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9.3: Amino Acids, Proteins, and pH

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    52403
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    In addition to examining how adding a strong acid or base affects a buffer solution, we can also look at the effect of pH on a particular acid or base. This is particularly important in biological systems where there are many weak acid or base groups that can be affected by the pH. For example, proteins contain both weakly acidic –COOH and weakly basic –NH2 groups. A 1.0-M solution of a simple carboxylic acid like acetic acid has a pH of ~ 2.8; it turns out that most carboxylic acids behave in a similar way. If we manipulate the pH, for example, by adding a strong base, the acetic acid reacts with the base to form an acetate ion. Based on the Henderson– Hasselbalch equation, when [acetate] = [acetic acid], the pH equals the acid’s pKa, which is 4.74. As the pH increases, the concentration of acetate must also increase, until by pH ~7 (approximately normal physiological pH). At this point the concentration of acetic acid is very small indeed. The ratio of base to acid is about 200/1. That is, at physiological pHs groups such as carboxylic acids are deprotonated and exist in the carboxylate (negatively charged) form.

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    Conversely, if we look at the amino group (–NH2) of a protein, it is actually the base part of a conjugate acid-base pair in which the acid is the protonated form –NH3+. The pKa of an –NH3+ group is typically ~9. At a pH of 9 there are equal amounts of the protonated (– NH2) and unprotonated forms (–NH3+). So if we change the pH by adding an acid, the concentration of – NH3+ form increases as the base form –NH2 is protonated. At pH ~7 there is little of the –NH2 form remaining.

    Interestingly, this means that an amino acid (shown in the figure) never exists in a state where both the amino (–NH2) group and the carboxylic acid (–CO2H) exist at the same time. The “neutral” species is in fact the one in which –NH3+/–CO2are present. This zwitterion (that is a neutral molecules with a positive and negative electrical charge at different locations, from the German zwitter, meaning “between”) is the predominant form at physiological pH.

    A protein is composed mainly (sometimes solely) of polymers of amino acids, known as polypeptides. In a polypeptide, the amino (–NH2) and carboxylic acid (–CO2H) groups of amino acids are bonded together to form a peptide bond (see figure). page196image22992

    The resulting amide group (peptide bond) is neither acidic nor basic under physiological conditions182. That being said, many of the amino acids found in proteins have acidic (aspartic acid or glutamic acid) or basic (lysine, arginine, or histidine) side chains. The pH of the environment influences the conformations of the protein molecule and the interactions between these charged side chains (the spontaneous native conformations of the molecule are called protein folding). Changes from the “normal” environment can lead to changes in protein structure, and this in turn can change biological activity. In some cases, protein activity is regulated by environmental pH. In other cases, changes in pH can lead to protein misfolding (or denaturation, which in living organisms can cause disruption of cell activity or death). For example,: if these groups are protonated or deprotonated, the electronic environment in that region of the protein can change drastically, which may mean that the protein will not only change how it interacts with other species but its shape may change so as to minimize repulsive interactions or produce new attractive interactions. Small changes in protein shape can have profound effects on how the protein interacts with other molecules and, if it is a catalyst, its efficiency and specificity. In fact, there are cases where environmental pH is used to regulate protein activity.

    Questions to Answer

    • What would be the ratio of –NH3+/–NH2 in a solution of a protein at pH 5 , pH 7, and pH 9?

    • What kinds of interactions would each form participate in?

    • What is the predominant form of a carboxylic acid group at pH 5? pH 7? pH 9?

    • What kinds of interactions would each form participate in?

    • What is the ratio of –NH3+/–NH2 in a solution of a protein at pH 5, pH 7, and pH 9? What kinds of interactions does each form participate in?

    • What is the predominant form of a carboxylic acid group at pH 5? How about at pH 7 and pH 9? What kinds of interactions does each form participate in?

    References

    182 You might wonder why the amide nitrogen is not basic - even though it appears to have a lone pair of electrons. However these electrons are not available for donation because they are conjugated (interacting) with the C=O group. You will have to wait until organic chemistry to hear more on this fascinating topic


    9.3: Amino Acids, Proteins, and pH is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by LibreTexts.

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