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使用工程化BRET报告基因对肿瘤生物学进行优化的多光谱生物发光成像。

Optimized multispectral bioluminescent imaging of tumor biology using engineered BRET reporters.

作者信息

Labra Bryan, Parag-Sharma Kshitij, Powers John J, Srivastava Sonal, Walker Joel R, Kirkland Thomas A, Brennan Caroline K, Prescher Jennifer A, Amelio Antonio L

机构信息

Lineberger Comprehensive Cancer Center, UNC School of Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Graduate Curriculum in Cell Biology & Physiology, Biological & Biomedical Sciences Program, UNC School of Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

出版信息

iScience. 2024 Aug 8;27(9):110655. doi: 10.1016/j.isci.2024.110655. eCollection 2024 Sep 20.

DOI:10.1016/j.isci.2024.110655
PMID:39252965
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11381837/
Abstract

The ability to visualize and track multiple biological processes in real time is highly desirable. Bioluminescence imaging (BLI) has emerged as an attractive modality for non-invasive cell tracking, with various luciferase reporters enabling parallel monitoring of several processes. However, simultaneous multiplexed imaging is challenging due to suboptimal reporter intensities and the need to image one luciferase at a time. We report a multiplexed BLI approach using a single substrate that leverages bioluminescence resonance energy transfer (BRET)-based reporters with distinct spectral profiles for triple-color BLI. These luciferase-fluorophore fusion reporters address light transmission challenges and use optimized coelenterazine substrates. Comparing BRET reporters across two substrate analogs identified a green-yellow-orange combination that allows simultaneous imaging of three distinct cell populations and . These tools provide a template for imaging other biological processes during a single BLI session using a single reporter substrate.

摘要

能够实时可视化和跟踪多个生物过程是非常理想的。生物发光成像(BLI)已成为一种有吸引力的非侵入性细胞跟踪方式,各种荧光素酶报告基因能够对多个过程进行并行监测。然而,由于报告基因强度不理想以及需要一次对一种荧光素酶进行成像,同时进行多重成像具有挑战性。我们报告了一种使用单一底物的多重BLI方法,该方法利用基于生物发光共振能量转移(BRET)的报告基因,这些报告基因具有不同的光谱特征,用于三色BLI。这些荧光素酶 - 荧光团融合报告基因解决了光传输挑战,并使用了优化的腔肠素底物。比较两种底物类似物的BRET报告基因,确定了一种绿 - 黄 - 橙组合,该组合允许同时对三个不同的细胞群体进行成像。这些工具为在使用单一报告基因底物的单个BLI实验期间对其他生物过程进行成像提供了一个模板。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/281a/11381837/1b1d2b11bc57/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/281a/11381837/597f78b430dc/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/281a/11381837/c445c2d698dd/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/281a/11381837/86de4ab25c0d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/281a/11381837/1b1d2b11bc57/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/281a/11381837/597f78b430dc/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/281a/11381837/c445c2d698dd/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/281a/11381837/86de4ab25c0d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/281a/11381837/1b1d2b11bc57/gr3.jpg

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