Abstract
The specific interaction between sense and antisense peptides was studied by high-performance affinity chromatography (HPAC) and quartz crystal microbalance (QCM) biosensor. Fragment 1–14 of human interferon-β (hIFN-β) was chosen as sense peptide and its three antisense peptides (AS-IFN 1, AS-IFN 2, and AS-IFN 3) were designed according to the degeneracy of genetic codes. The affinity column was prepared with sense peptide as ligand and the affinity chromatographic behavior was evaluated. Glu-substituted antisense peptide (AS-IFN 3) showed the strongest binding to immobilized sense peptide at pH 7.5. A quartz crystal microbalance-flow injection analysis (QCM-FIA) system was introduced to investigate the recognition process in real-time. The equilibrium dissociation constants between sense peptide and AS-IFN 1, AS-IFN 2 and AS-IFN 3 measured 2.08×10−4, 1.31×10−4 and 2.22×10−5 mol/L, respectively. The mechanism study indicated that the specific recognition between sense peptide and AS-IFN 3 was due to sequence-dependent and multi-modal affinity interaction.
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Supported by the National Natural Science Foundation of China (Grant Nos. 20575072, 20435030 and 90408018) and the Chinese Academy of Sciences (Grant No. KJCX2-SW-H06)
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Luo, J., Huang, Y., Xiong, S. et al. Study on peptide-peptide interaction using high-performance affinity chromatography and quartz crystal microbalance biosensor. CHINESE SCI BULL 52, 1311–1319 (2007). https://doi.org/10.1007/s11434-007-0175-3
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DOI: https://doi.org/10.1007/s11434-007-0175-3