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单壁碳纳米管和序列可调肽聚合物的静电组装可检测凝集素蛋白及其靶糖。

Electrostatic Assemblies of Single-Walled Carbon Nanotubes and Sequence-Tunable Peptoid Polymers Detect a Lectin Protein and Its Target Sugars.

机构信息

Department of Chemical and Biomolecular Engineering , University of California, Berkeley , Berkeley , California 94720 , United States.

The Molecular Foundry , Lawrence Berkeley National Laboratory , 1 Cyclotron Road , Berkeley , California 94720 , United States.

出版信息

Nano Lett. 2019 Nov 13;19(11):7563-7572. doi: 10.1021/acs.nanolett.8b04955. Epub 2019 Apr 19.

Abstract

A primary limitation to real-time imaging of metabolites and proteins has been the selective detection of biomolecules that have no naturally occurring or stable molecular recognition counterparts. We present developments in the design of synthetic near-infrared fluorescent nanosensors based on the fluorescence modulation of single-walled carbon nanotubes (SWNTs) with select sequences of surface-adsorbed N-substituted glycine peptoid polymers. We assess the stability of the peptoid-SWNT nanosensor candidates under variable ionic strengths, protease exposure, and cell culture media conditions and find that the stability of peptoid-SWNTs depends on the composition and length of the peptoid polymer. From our library, we identify a peptoid-SWNT assembly that can detect lectin protein wheat germ agglutinin (WGA) with a sensitivity comparable to the concentration of serum proteins. To demonstrate the retention of nanosensor-bound protein activity, we show that WGA on the nanosensor produces an additional fluorescent signal modulation upon exposure to the lectin's target sugars, suggesting the lectin protein remains active and selectively binds its target sugars through ternary molecular recognition interactions relayed to the nanosensor. Our results inform design considerations for developing synthetic molecular recognition elements by assembling peptoid polymers on SWNTs and also demonstrate these assemblies can serve as optical nanosensors for lectin proteins and their target sugars. Together, these data suggest certain peptoid sequences can be assembled with SWNTs to serve as versatile optical probes to detect proteins and their molecular substrates.

摘要

实时成像代谢物和蛋白质的主要限制因素一直是选择性检测没有天然存在或稳定分子识别对应物的生物分子。我们介绍了基于表面吸附的 N-取代甘氨酸肽聚合物的选择序列对单壁碳纳米管(SWNTs)的荧光调制来设计合成近红外荧光纳米传感器的进展。我们评估了在不同离子强度、蛋白酶暴露和细胞培养基条件下肽-SWNT 纳米传感器候选物的稳定性,发现肽-SWNTs 的稳定性取决于肽聚合物的组成和长度。在我们的文库中,我们确定了一种肽-SWNT 组装体,它可以检测凝集素蛋白麦胚凝集素(WGA),其灵敏度与血清蛋白的浓度相当。为了证明纳米传感器结合蛋白的活性保持不变,我们表明纳米传感器上的 WGA 在暴露于凝集素的靶糖时会产生额外的荧光信号调制,这表明凝集素蛋白仍然保持活性,并通过传递到纳米传感器的三元分子识别相互作用选择性地结合其靶糖。我们的结果为通过将肽聚合物组装到 SWNTs 上开发合成分子识别元件提供了设计考虑因素,并且还证明了这些组装体可以作为凝集素蛋白及其靶糖的光学纳米传感器。这些数据表明,某些肽序列可以与 SWNTs 组装在一起,作为检测蛋白质及其分子底物的多功能光学探针。

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