Literature DB >> 34541724

Construction of Messenger RNA (mRNA) Probes Delivered By Lipid Nanoparticles to Visualize Intracellular Protein Expression and Localization at Organelles.

Weiyu Zhao1, Chunxi Zeng1, Jingyue Yan1, Shi Du1, Xucheng Hou1, Chengxiang Zhang1, Wenqing Li1, Binbin Deng2, David W McComb2, Yonger Xue1, Diana D Kang1, Yizhou Dong1,3.   

Abstract

Organelles are specialized compartments, where various proteins reside and play crucial roles to maintain essential cellular structures and functions in mammalian cells. A comprehensive understanding of protein expressions and subsequent localizations at each organelle is of great benefit to the development of organelle-based therapies. Herein, a set of single or dual organelle labeling messenger RNAs (SOLAR or DOLAR) is designed as novel imaging probes, which encode fluorescent proteins with various organelle localization signals. These mRNA probes enable to visualize the protein localizations at different organelles and investigate their trafficking from ribosomal machinery to specific organelles. According to the in vitro results, SOLAR probes show organelle targeting capabilities consistent with the design. Moreover, DOLAR probes with different linkers display distinct targeting properties depending on different organelle localization signals. Additionally, these mRNA probes also exhibit organelle labeling ability in vivo when delivered by lipid nanoparticles (LNPs). Therefore, these mRNA-based probes provide a unique tool to study cell organelles and may facilitate the design of organelle-based therapies.
© 2021 Wiley-VCH GmbH.

Entities:  

Keywords:  lipid nanoparticles; mRNA probes; organelle targeting; protein translocation

Mesh:

Substances:

Year:  2021        PMID: 34541724      PMCID: PMC8578456          DOI: 10.1002/adma.202103131

Source DB:  PubMed          Journal:  Adv Mater        ISSN: 0935-9648            Impact factor:   32.086


  35 in total

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Review 10.  Mitochondria-Associated Membranes As Networking Platforms and Regulators of Cancer Cell Fate.

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