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解析甲卡西酮适体的结合模式:光谱和量热研究。

Unraveling the binding mode of a methamphetamine aptamer: A spectroscopic and calorimetric study.

机构信息

The MacDiarmid Institute for Advanced Materials and Nanotechnology, Victoria University of Wellington Wellington, New Zealand; School of Chemical and Physical Sciences, Victoria University of Wellington, Wellington, New Zealand.

Centre for Biodiscovery, School of Chemical and Physical Sciences, Victoria University of Wellington, Wellington, New Zealand.

出版信息

Biophys J. 2022 Jun 7;121(11):2193-2205. doi: 10.1016/j.bpj.2022.04.027. Epub 2022 Apr 26.

Abstract

Nucleic-acid aptamers are bio-molecular recognition agents that bind to their targets with high specificity and affinity and hold promise in a range of biosensor and therapeutic applications. In the case of small-molecule targets, their small size and limited number of functional groups constitute challenges for their detection by aptamer-based biosensors because bio-recognition events may both be weak and produce poorly transduced signals. The binding affinity is principally used to characterize aptamer-ligand interactions; however, a structural understanding of bio-recognition is arguably more valuable in order to design a strong response in biosensor applications. Using a combination of nuclear magnetic resonance, circular dichroism, and isothermal titration calorimetry, we propose a binding model for a new methamphetamine aptamer and determine the main interactions driving complex formation. These measurements reveal only modest structural changes to the aptamer upon binding and are consistent with a conformational-selection binding model. The aptamer-methamphetamine complex formation was observed to be entropically driven, apparently involving hydrophobic and electrostatic interactions. Taken together, our results exemplify a means of elucidating small molecule-aptamer binding interactions, which may be decisive in the development of aptasensors and therapeutics and may contribute to a deeper understanding of interactions driving aptamer selection.

摘要

核酸适体是生物分子识别剂,它们与靶标具有高度特异性和亲和力,并在一系列生物传感器和治疗应用中具有广阔的应用前景。在小分子靶标的情况下,由于生物识别事件可能既弱又产生转导信号不良,它们的小尺寸和有限数量的官能团构成了基于适体的生物传感器检测的挑战。结合核磁共振、圆二色性和等温滴定量热法,我们提出了一种新的甲基苯丙胺适体的结合模型,并确定了驱动复合物形成的主要相互作用。这些测量结果表明,适体结合后只有适度的结构变化,与构象选择结合模型一致。观察到适体-甲基苯丙胺复合物的形成是熵驱动的,显然涉及疏水相互作用和静电相互作用。总之,我们的结果说明了阐明小分子-适体结合相互作用的一种方法,这可能对适体传感器和治疗剂的开发具有决定性意义,并可能有助于深入了解驱动适体选择的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cf7/9247340/21e925d8eac2/fx1.jpg

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