吡唑酮-蛋白质相互作用可在细胞膜上实现长期保留染色和简便的人工生物识别。

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of the American Chemical Society Pub Date : 2024-08-28 Epub Date: 2024-08-13 DOI:10.1021/jacs.4c08987
Tao Xiong, Yingchao Chen, Qiang Peng, Mingle Li, Sheng Lu, Xiaoqiang Chen, Jiangli Fan, Lei Wang, Xiaojun Peng
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引用次数: 0

摘要

细胞膜基因工程已被用于赋予细胞膜以诊断和治疗目的的功能,但人们对成本和可变修饰结果表示担忧。虽然非遗传化学修饰和磷脂插入策略更为方便,但它们仍然面临着生物安全性或修饰稳定性方面的瓶颈。在本文中,我们发现含有吡唑酮的分子能以高稳定性与蛋白质结合,这主要得益于吡唑酮与碱性氨基酸之间的多重相互作用。这种新的结合模式为细胞膜功能化提供了一种简单而多用途的非共价方法。通过与细胞膜蛋白结合,含有吡唑啉酮的染料能够在体外(>96 小时)和体内(>21 天)精确追踪细胞,而不会干扰蛋白功能或导致细胞死亡。此外,含吡唑啉酮的生物素可方便地锚定在细胞膜上,使其具有与阿维丁类似的生物识别能力,显示了人工制造细胞靶向性的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Pyrazolone-Protein Interaction Enables Long-Term Retention Staining and Facile Artificial Biorecognition on Cell Membranes.

Cell membrane genetic engineering has been utilized to confer cell membranes with functionalities for diagnostic and therapeutic purposes but concerns over cost and variable modification results. Although nongenetic chemical modification and phospholipid insertion strategies are more convenient, they still face bottlenecks in either biosafety or stability of the modifications. Herein, we show that pyrazolone-bearing molecules can bind to proteins with high stability, which is mainly contributed to by the multiple interactions between pyrazolone and basic amino acids. This new binding model offers a simple and versatile noncovalent approach for cell membrane functionalization. By binding to cell membrane proteins, pyrazolone-bearing dyes enabled precise cell tracking in vitro (>96 h) and in vivo (>21 days) without interfering with the protein function or causing cell death. Furthermore, the convenient anchor of pyrazolone-bearing biotin on cell membranes rendered the biorecognition to avidin, showing the potential for artificially creating cell targetability.

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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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