Self-Immobilizing Fluorogenic Probe for In Situ Labeling of Granzyme B Activity in Host Immune Response to Bacterial Infections.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
ChemBioChem Pub Date : 2025-01-22 DOI:10.1002/cbic.202400990
Rao Wei, Ling Lei, Ling-Ling Wu, Leilei Zhang, Hai-Yu Hu
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Abstract

Bacterial infections, particularly those caused by drug-resistant bacteria, represent a pressing global health challenge. During the interaction between pathogen infection and host defense, bacterial infections initiate the host's immune response, which involves the activation of proteases that play a critical role in antibacterial defense. Granzyme B (GzmB), a key immune-related biomarker associated with cytotoxic T lymphocytes (CTLs), plays a pivotal role in this process. Therefore, detecting the activity of GzmB is crucial for understanding the host immune response to bacterial infections and for developing therapeutic strategies to overcome bacterial virulence. In this study, we designed and synthesized three granzyme B-activated near-infrared molecular probes. Among them, the probe HCy-F demonstrates in situ imaging capability, enabling precise quantification of GzmB activity. This development offers a valuable tool for monitoring immune responses and optimizing immunotherapy approaches for combating drug-resistant pathogens.

自固定荧光探针原位标记颗粒酶B在宿主对细菌感染免疫反应中的活性。
细菌感染,特别是由耐药细菌引起的细菌感染,是一项紧迫的全球卫生挑战。在病原体感染和宿主防御的相互作用中,细菌感染启动宿主的免疫反应,其中涉及在抗菌防御中起关键作用的蛋白酶的激活。颗粒酶B (GzmB)是一种与细胞毒性T淋巴细胞(ctl)相关的关键免疫相关生物标志物,在这一过程中起着关键作用。因此,检测GzmB的活性对于了解宿主对细菌感染的免疫反应以及制定克服细菌毒力的治疗策略至关重要。在本研究中,我们设计并合成了三种颗粒酶b激活的近红外分子探针。其中,探针HCy-F具有原位成像能力,能够精确量化GzmB活性。这一进展为监测免疫反应和优化免疫治疗方法以对抗耐药病原体提供了有价值的工具。
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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来源期刊
ChemBioChem
ChemBioChem 生物-生化与分子生物学
CiteScore
6.10
自引率
3.10%
发文量
407
审稿时长
1 months
期刊介绍: ChemBioChem (Impact Factor 2018: 2.641) publishes important breakthroughs across all areas at the interface of chemistry and biology, including the fields of chemical biology, bioorganic chemistry, bioinorganic chemistry, synthetic biology, biocatalysis, bionanotechnology, and biomaterials. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and supported by the Asian Chemical Editorial Society (ACES).
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