The isoelectric point (pI) of a protein is the pH at which it carries no net charge, with protonation and deprotonation of amino acid side chains affecting its charge at different pH levels. At the pI, the number of positively charged side chains equals the number of negatively charged ones, which can facilitate protein crystallization. The relationship between protein structure and pI is debated, with some suggesting that proteins rich in beta-structure may have lower pI values compared to those rich in alpha-structure, though this is not widely established. Observations from isoelectric focusing (IEF) gels indicate that proteins with low pI often contain more beta-strands, raising questions about potential correlations. Understanding these dynamics is crucial for effective protein crystallization and characterization.