Red light-emitting short Mango-based system enables tracking a mycobacterial small noncoding RNA in infected macrophages

Author:

Bychenko Oksana S1,Khrulev Alexei A1,Svetlova Julia I2,Tsvetkov Vladimir B23ORCID,Kamzeeva Polina N1,Skvortsova Yulia V1,Tupertsev Boris S4,Ivanov Igor A1,Aseev Leonid V1,Khodarovich Yuriy M1,Belyaev Evgeny S5,Kozlovskaya Liubov I67,Zatsepin Timofei S8,Azhikina Tatyana L1,Varizhuk Anna M29,Aralov Andrey V1ORCID

Affiliation:

1. Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences , Moscow  117997, Russia

2. Federal Research and Clinical Center of Physical-Chemical Medicine , Moscow  119435, Russia

3. Institute of Biodesign and Complex System Modeling, I.M. Sechenov First Moscow State Medical University , Moscow  119991, Russia

4. Skolkovo Institute of Science and Technology , Moscow  121205, Russia

5. Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences , Moscow 119071, Russia

6. FSBSI Chumakov Federal Scientific Center for Research and Development of Immune and Biological Products, Russian Academy of Sciences , Moscow 108819, Russia

7. Institute of Translational Medicine and Biotechnology I.M. Sechenov First Moscow State Medical University , Moscow  119991, Russia

8. Lomonosov Moscow State University, Department of Chemistry ,  Moscow 119992 , Russia

9. Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency , Moscow  119435, Russia

Abstract

AbstractProgress in RNA metabolism and function studies relies largely on molecular imaging systems, including those comprising a fluorogenic dye and an aptamer-based fluorescence-activating tag. G4 aptamers of the Mango family, typically combined with a duplex/hairpin scaffold, activate the fluorescence of a green light-emitting dye TO1-biotin and hold great promise for intracellular RNA tracking. Here, we report a new Mango-based imaging platform. Its key advantages are the tunability of spectral properties and applicability for visualization of small RNA molecules that require minimal tag size. The former advantage is due to an expanded (green-to-red-emitting) palette of TO1-inspired fluorogenic dyes, and the truncated duplex scaffold ensures the latter. To illustrate the applicability of the improved platform, we tagged Mycobacterium tuberculosis sncRNA with the shortened aptamer-scaffold tag. Then, we visualized it in bacteria and bacteria-infected macrophages using the new red light-emitting Mango-activated dye.

Funder

Russian Foundation for Basic Research

Russian Science Foundation

Ministry of Science and Higher Education of the Russian Federation

Publisher

Oxford University Press (OUP)

Subject

Genetics

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