人癌细胞整合素受体的靶向- ters检测。

Lifu Xiao, Zachary D. Schultz
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引用次数: 3

摘要

膜受体在调节细胞活动中起着重要作用。靶向肿瘤细胞中的膜受体并了解其与特定配体的相互作用是癌症预后和治疗的关键。然而,需要开发新的技术来提供对细胞膜中配体-受体结合化学的分子洞察力。整合素受体是调控肿瘤细胞迁移、侵袭和增殖的重要膜受体。整合素对含有精氨酸-甘氨酸-天冬氨酸(RGD)序列的小肽配体具有众所周知的亲和力,因此是研究配体-受体相互作用的一个有吸引力的模型系统。我们最近报道了一种利用尖端增强拉曼散射(TERS)检测整合素受体并研究其与环rgdfc配体结合化学的方法。我们已经证明,由于RGD配体结合位点的差异,两种结构相似的整合素可以在完整的细胞膜中分化,这显示了这种TERS方法在研究其他膜受体及其在活细胞中的相互作用方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeted-TERS detection of integrin receptors on human cancer cells.
Membrane receptors play important roles in regulating cellular activities. Targeting membrane receptors in cancer cells and understanding their interactions with specific ligands are key for cancer prognosis and therapeutics. However, there is a need to develop new technologies to provide molecular insight into ligand-receptor binding chemistry in cell membrane. Integrin receptors are important membrane receptors that regulate cellular migration, invasion and proliferation in tumors. Integrins have a well-known affinity towards small peptide ligands containing arginine-glycine-aspartate (RGD) sequence and are therefore an attractive model system to study ligand-receptor interactions. We have recently reported a method to detect integrin receptors and study their binding chemistry with cyclic-RGDfC ligand using tip-enhanced Raman scattering (TERS). We have demonstrated that two integrins with similar structures can be differentiated in intact cell membrane, due to the differences in their RGD ligand binding sites, showing the potential of this TERS methodology to study other membrane receptors and their interactions in live cells.
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