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In Situ Visualizing the Recognition Between Proteins and Platinum-Damaged DNA in Single-Cells by Correlated Optical and Secondary Ion Mass Spectrometric Imaging

revised on 16.04.2020, 10:42 and posted on 20.04.2020, 06:02 by Yu Lin, Kui Wu, Feifei Jia, Ling Chen, Zhaoying Wang, Yanyan Zhang, Qun Luo, Suyan Liu, Luyu Qi, Nan Li, Xiaohong Fang, Pu Dong, Fei Gao, Yao Zhao, Fuyi Wang

In situ visualization of the recognition and interaction between proteins and drug damaged DNA at single cell level is highly important for understanding the molecular mechanism of action of DNA targeting drugs, yet a great challenge. We herein report a novel approach, termed as correlated optical and secondary ion mass spectrometric imaging (COSIMSi), for exploring the recognition between proteins and cisplatin-damaged DNA in single cells. Genetically encoded EYFP-fused HMGB1, an in vitro well-known specific binder of cisplatin-damaged DNA, and dye-stained DNA, and cisplatin were mapped by LSCM and ToF-SIMS imaging, respectively. The LSCM and SIMS images were aligned with aiding of an addressable silicon wafer to generate fused images, in which the co-localization of the fluorescence and MS signals indicated the formation of HMGB1-Pt-DNA ternary complexes in a dose- and time-dependent manner. In contrast, COSIMSi showed that little HMGB1(F37A)-Pt-DNA complex was produced under the same conditions. Moreover, we demonstrated for the first time that cisplatin lesion on DNA prevented a DNA-binding protein Smad3 from interacting with DNA. These results verify that the COSIMSi is an effective and straightforward tool for in situ visualization of recognition and interaction between proteins and specific damaged DNA in single cells.


Email Address of Submitting Author


Institute of Chemistry, Chinese Academy of Sciences



ORCID For Submitting Author


Declaration of Conflict of Interest

The authors declare no competing interests.