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用于定量血清和细胞内游离锌的比率型生物发光锌传感器蛋白

Ratiometric Bioluminescent Zinc Sensor Proteins to Quantify Serum and Intracellular Free Zn.

出版信息

ACS Chem Biol. 2022 Jun 17;17(6):1567-1576. doi: 10.1021/acschembio.2c00227. Epub 2022 May 25.

DOI:10.1021/acschembio.2c00227
PMID:35611686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9207811/
Abstract

Fluorescent Zn sensors play a pivotal role in zinc biology, but their application in complex media such as blood serum or plate reader-based cellular assays is hampered by autofluorescence and light scattering. Bioluminescent sensor proteins provide an attractive alternative to fluorescent sensors for these applications, but the only bioluminescent sensor protein developed so far, BLZinCh, has a limited sensor response and a suboptimal Zn affinity. In this work, we expanded the toolbox of bioluminescent Zn sensors by developing two new sensor families that show a large change in the emission ratio and cover a range of physiologically relevant Zn affinities. The LuZi platform relies on competitive complementation of split NanoLuc luciferase and displays a robust, 2-fold change in red-to-blue emission, allowing quantification of free Zn between 2 pM and 1 nM. The second platform was developed by replacing the long flexible GGS linker in the original BLZinCh sensor by rigid polyproline linkers, yielding a series of BLZinCh-Pro sensors with a 3-4-fold improved ratiometric response and physiologically relevant Zn affinities between 0.5 and 1 nM. Both the LuZi and BLZinCh-Pro sensors allowed the direct determination of low nM concentrations of free Zn in serum, providing an attractive alternative to more laborious and/or indirect approaches to measure serum zinc levels. Furthermore, the genetic encoding of the BLZinCh-Pro sensors allowed their use as intracellular sensors, where the sensor occupancy of 40-50% makes them ideally suited to monitor both increases and decreases in intracellular free Zn concentration in simple, plate reader-based measurements, without the need for fluorescence microscopy.

摘要

荧光锌传感器在锌生物学中起着至关重要的作用,但它们在血清或基于平板读数器的细胞测定等复杂介质中的应用受到自发荧光和光散射的阻碍。生物发光传感器蛋白为这些应用提供了一种有吸引力的荧光传感器替代方案,但迄今为止开发的唯一生物发光传感器蛋白 BLZinCh 的传感器响应有限,锌亲和力也不理想。在这项工作中,我们通过开发两种新的传感器家族来扩展生物发光锌传感器的工具包,这些家族在发射比上有很大的变化,并覆盖了一系列生理相关的锌亲和力范围。LuZi 平台依赖于分割 NanoLuc 荧光酶的竞争性互补,显示出强大的红色到蓝色发射的 2 倍变化,允许在 2 pM 至 1 nM 之间定量游离锌。第二个平台是通过用刚性聚脯氨酸接头替代原始 BLZinCh 传感器中的长柔性 GGS 接头来开发的,产生了一系列 BLZinCh-Pro 传感器,其比率响应提高了 3-4 倍,生理相关的锌亲和力在 0.5 和 1 nM 之间。LuZi 和 BLZinCh-Pro 传感器都允许直接测定血清中低 nM 浓度的游离锌,为更繁琐和/或间接测定血清锌水平提供了一种有吸引力的替代方法。此外,BLZinCh-Pro 传感器的遗传编码允许它们作为细胞内传感器使用,其中传感器占有率为 40-50%,使其非常适合在简单的基于平板读数器的测量中监测细胞内游离锌浓度的增加和减少,而无需荧光显微镜。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1476/9207811/f5ca6e60b46f/cb2c00227_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1476/9207811/333b1cbf8145/cb2c00227_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1476/9207811/3b96ffbd77cb/cb2c00227_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1476/9207811/57db76122ace/cb2c00227_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1476/9207811/a90f4bde43af/cb2c00227_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1476/9207811/f5ca6e60b46f/cb2c00227_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1476/9207811/333b1cbf8145/cb2c00227_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1476/9207811/3b96ffbd77cb/cb2c00227_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1476/9207811/57db76122ace/cb2c00227_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1476/9207811/a90f4bde43af/cb2c00227_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1476/9207811/f5ca6e60b46f/cb2c00227_0005.jpg

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