What does high pressure liquid chromatography primarily measure in relation to proteins?

Prepare for the UofT BCH210H1 Biochemistry I midterm with exam-like questions. Access detailed solutions and explanations for proteins, lipids, and metabolism topics. Strengthen your understanding and excel on test day!

High-pressure liquid chromatography (HPLC) is a vital technique in biochemistry, particularly for analyzing proteins. The primary measurement it relies on is the time a protein spends on a chromatographic column, known as retention time, which is influenced by the interaction of the protein with the stationary phase of the column.

During HPLC, proteins in a sample are separated based on their unique properties such as size, charge, or hydrophobicity as they travel through the column. Each protein interacts differently with the stationary phase, determining its retention time. These retention times can then be used to identify or quantify proteins when compared against known standards. Additionally, absorbance is measured as proteins elute from the column; this allows for the detection and quantification of the proteins present in the sample. The absorbance value at specific wavelengths is often used to track the proteins, particularly at 280 nm for aromatic amino acids.

Other options do not adequately represent the primary functions of HPLC. The pH of the protein solution does not influence the fundamental measurement in HPLC but can affect protein behavior in solutions. The temperature of the chromatographic column might impact the flow rate or interaction, but is not directly measured by the system for protein analysis. Finally, while molecular weight

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