Raman spectroscopic analysis of highly-concentrated antibodies under the acid-treated conditions

拉曼光谱 化学 变性(裂变材料) 构象变化 分子间力 胶体 生物物理学 分析化学(期刊) 色谱法 生物化学 分子 物理化学 核化学 有机化学 生物 光学 物理
作者
Yoji Sato,Satoru Nagatoishi,Shintaro Noguchi,Kouhei Tsumoto
出处
期刊:Cornell University - arXiv
标识
DOI:10.48550/arxiv.2207.06556
摘要

Antibody drugs are usually formulated as highly-concentrated solutions, which would easily generate oligomer and aggregation, resulting in loss of efficacy. Although low pH increases the colloidal dispersion of antibodies, acid denaturation can be an issue. Therefore, knowing the physical properties of antibodies at low pH under high concentration conditions is an important insight into the quality evaluation of high concentration antibodies. Raman spectroscopy is a powerful tool to obtain conformational information derived from amino acid residues and secondary structures without dilution. In this study, Raman spectroscopy was used to investigate pH-induced conformational changes of antibodies at high concentrations. Raman experiments in pH 3 to 7 were performed for human serum IgG and recombinant rituximab. We detected the evident changes at pH 3 in Tyr and Trp Raman bands, which are the sensitive markers of intermolecular interactions. Thermal transition analysis over the pH range demonstrated that the transition temperature (aggregation temperature, Tagg) was highest at pH 3. Acid-treated and neutralized one showed higher Tagg than that of pH 7, indicating that acid-induced conformational changes were not completely reversible. Colloidal analyses confirmed the findings of the Raman analysis, validating Raman spectroscopy as a method for evaluating antibody conformation associated with colloidal information.

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