Assembly of long L-RNA by native RNA ligation.


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
12 Oct 2021
Historique:
pubmed: 23 9 2021
medline: 30 11 2021
entrez: 22 9 2021
Statut: epublish

Résumé

Due to their intrinsic nuclease resistance, L-oligonucleotides are being increasingly utilized in the development of molecular tools and sensors. Yet, it remains challenging to synthesize long L-oligonucleotides, potential limiting future applications. Herein, we report straightforward and versitile approach to assemble long L-RNAs from two or more shorter fragments using T4 RNA ligase 1. We show that this approach is compatible with the assembly of several classes of functional L-RNA, which we highlight by generating a 124 nt L-RNA biosensor that functions in serum.

Identifiants

pubmed: 34550128
doi: 10.1039/d1cc04296c
pmc: PMC8641125
mid: NIHMS1756061
doi:

Substances chimiques

Viral Proteins 0
RNA 63231-63-0
RNA Ligase (ATP) EC 6.5.1.3
bacteriophage T4 RNA ligase 1 EC 6.5.1.3

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

10508-10511

Subventions

Organisme : NIGMS NIH HHS
ID : R35 GM124974
Pays : United States

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Auteurs

Chen-Hsu Yu (CH)

Department of Chemistry, Texas A&M University, College Station, TX, USA. jon.sczepanski@chem.tamu.edu.

Adam M Kabza (AM)

Department of Chemistry, Texas A&M University, College Station, TX, USA. jon.sczepanski@chem.tamu.edu.

Jonathan T Sczepanski (JT)

Department of Chemistry, Texas A&M University, College Station, TX, USA. jon.sczepanski@chem.tamu.edu.

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Classifications MeSH