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使用光学成像技术在体和无标记定量检测膜蛋白-配体相互作用:综述。

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

机构信息

School of Pharmacy, Xinxiang Medical University, Xinxiang 453003, China.

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.

出版信息

Biosensors (Basel). 2024 Nov 6;14(11):537. doi: 10.3390/bios14110537.

Abstract

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.

摘要

膜蛋白对于各种细胞过程至关重要,是药理学研究的关键靶点。它们与配体的相互作用对于阐明细胞机制和推进药物开发至关重要。为了在天然环境中研究这些相互作用而不改变其功能特性,已经开发了几种先进的光学成像方法用于原位和无标记定量。本综述重点介绍了最近的光学成像技术,如表面等离子体共振成像(SPRi)、表面等离子体共振显微镜(SPRM)、边缘跟踪方法和表面光散射显微镜(SLSM)。我们探讨了这些方法的工作原理、最新进展以及应用范围。此外,我们还讨论了这些创新光学成像策略目前所面临的挑战,并探讨了它们在加深我们对生物分子相互作用的理解和促进新型治疗剂发现方面的未来潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f46/11592237/46f96e439385/biosensors-14-00537-g001.jpg

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