In Situ and Label-Free Quantification of Membrane Protein-Ligand Interactions Using Optical Imaging Techniques: A Review

被引:1
|
作者
Huang, Caixin [1 ,2 ]
Zhang, Jingbo [2 ,3 ]
Liu, Zhaoyang [2 ,3 ]
Xu, Jiying [2 ,3 ]
Zhao, Ying [1 ]
Zhang, Pengfei [2 ,3 ]
机构
[1] Xinxiang Med Univ, Sch Pharm, Xinxiang 453003, Peoples R China
[2] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, Key Lab Analyt Chem Living Biosyst, Beijing 100190, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
来源
BIOSENSORS-BASEL | 2024年 / 14卷 / 11期
基金
北京市自然科学基金;
关键词
membrane protein-ligand interactions; binding kinetics; label-free quantification; optical imaging techniques; drug screening; BINDING-KINETICS; CELL-SURFACES; TRACKING; OPINION; TIME;
D O I
10.3390/bios14110537
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Membrane proteins are crucial for various cellular processes and are key targets in pharmacological research. Their interactions with ligands are essential for elucidating cellular mechanisms and advancing drug development. To study these interactions without altering their functional properties in native environments, several advanced optical imaging methods have been developed for in situ and label-free quantification. This review focuses on recent optical imaging techniques such as surface plasmon resonance imaging (SPRi), surface plasmon resonance microscopy (SPRM), edge tracking approaches, and surface light scattering microscopy (SLSM). We explore the operational principles, recent advancements, and the scope of application of these methods. Additionally, we address the current challenges and explore the future potential of these innovative optical imaging strategies in deepening our understanding of biomolecular interactions and facilitating the discovery of new therapeutic agents.
引用
收藏
页数:19
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