组织蛋白酶B
费斯特共振能量转移
组织蛋白酶D
化学
组织蛋白酶
荧光
分子生物学
生物化学
酶
生物
量子力学
物理
作者
Zhengxiao Zhang,Eiji Nakata,Yuya Shibano,Takashi Morii
出处
期刊:ChemBioChem
[Wiley]
日期:2022-08-05
卷期号:23 (19)
被引量:4
标识
DOI:10.1002/cbic.202200319
摘要
Abstract Fluorescent cathepsin probes were prepared by modification of peptidic substrates for cathepsin B (CTSB) and cathepsin D (CTSD) with FRET pairs. Fluorophores with distinguishable emission characteristics were applied to CTSB and CTSD probes with their appropriate quenchers to simultaneously monitor the activity of CTSB and/or CTSD. Conjugation of both the CTSB and CTSD probes with short single‐stranded DNA drastically increased their reactivity to cathepsins over the parent probes possibly by improving their solubility. The activity of CTSB and CTSD were simultaneously detected by using these orthogonal FRET‐based cathepsin probes.
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