用于迁移小体标记的aie活性近红外分子探针

IF 12.9 1区 医学 Q1 ENGINEERING, BIOMEDICAL Biomaterials Pub Date : 2025-08-01 Epub Date: 2025-02-27 DOI:10.1016/j.biomaterials.2025.123213
Jie Cui , Fei Zhang , Dong Jiang , Boqi Liu , Han Zhang , Niu Niu , Dingyuan Yan , Guangjie Song , Xue Li , Li Yu , Dong Wang , Ben Zhong Tang
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引用次数: 0

摘要

偏头痛小体是一种新发现的细胞器,在胚胎发生、免疫反应、伤口愈合和癌细胞转移等多种生理和病理活动中发挥着重要作用。迁徙小体可视化是深入探索迁徙小体生物学的必要条件。尽管报道了基于迁移小体标记蛋白的标记方法,但与复杂的转染技术相比,更需要一种简单方便的迁移小体标记方法。本文提出了一种基于聚集诱导发射(AIE)的近红外(NIR)分子探针TTCPy,它可以与偏头痛小体上的磷脂结合,并通过开启近红外荧光点亮偏头痛小体。TTCPy允许通过简单快速的染色对活细胞和活绒毛膜尿囊膜的迁移体进行高性能成像。此外,TTCPy实现了迁移体的活细胞超分辨率成像,提供了显著提高的空间分辨率和信本比。这项工作为迁移体可视化提供了一个简单而强大的工具,并将为迁移体生物学的蓬勃发展做出贡献。
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An AIE-active near-infrared molecular probe for migrasome labeling
Migrasomes, newly identified organelles, play crucial roles in various physiological and pathological activities, including embryogenesis, immune responses, wound healing, and metastasis of cancer cells. Migrasome visualization is essential for the deep exploration of migrasome biology. Despite the reported labeling methods based on migrasome marker proteins, a simple and convenient method for migrasome labeling is more desirable compared to the complicated transfection technique. Here, an aggregation-induced emission (AIE) based near-infrared (NIR) molecular probe named TTCPy was presented, which can bind to the phospholipid on migrasomes and light up migrasomes with a turn-on NIR fluorescence. TTCPy allows for high-performance imaging of migrasomes in both live cells and living chorioallantoic membranes via simple and rapid staining. Moreover, TTCPy achieves live-cell super-resolution imaging of migrasomes, affording remarkedly improved spatial resolution and signal-to-background ratio. This work offers a simple yet powerful tool for migrasome visualization and will contribute to the booming hotspot of migrasome biology.
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来源期刊
Biomaterials
Biomaterials 工程技术-材料科学:生物材料
CiteScore
26.00
自引率
2.90%
发文量
565
审稿时长
46 days
期刊介绍: Biomaterials is an international journal covering the science and clinical application of biomaterials. A biomaterial is now defined as a substance that has been engineered to take a form which, alone or as part of a complex system, is used to direct, by control of interactions with components of living systems, the course of any therapeutic or diagnostic procedure. It is the aim of the journal to provide a peer-reviewed forum for the publication of original papers and authoritative review and opinion papers dealing with the most important issues facing the use of biomaterials in clinical practice. The scope of the journal covers the wide range of physical, biological and chemical sciences that underpin the design of biomaterials and the clinical disciplines in which they are used. These sciences include polymer synthesis and characterization, drug and gene vector design, the biology of the host response, immunology and toxicology and self assembly at the nanoscale. Clinical applications include the therapies of medical technology and regenerative medicine in all clinical disciplines, and diagnostic systems that reply on innovative contrast and sensing agents. The journal is relevant to areas such as cancer diagnosis and therapy, implantable devices, drug delivery systems, gene vectors, bionanotechnology and tissue engineering.
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