Synthesis of Ortho‐Functionalized Tetrachlorinated Azobenzene Phosphoramidites for Incorporation Into siRNAzos for Photocontrolled Gene Silencing. Issue 8 (23rd August 2022)
- Record Type:
- Journal Article
- Title:
- Synthesis of Ortho‐Functionalized Tetrachlorinated Azobenzene Phosphoramidites for Incorporation Into siRNAzos for Photocontrolled Gene Silencing. Issue 8 (23rd August 2022)
- Main Title:
- Synthesis of Ortho‐Functionalized Tetrachlorinated Azobenzene Phosphoramidites for Incorporation Into siRNAzos for Photocontrolled Gene Silencing
- Authors:
- Hammill, Matthew L.
Islam, Golam
Desaulniers, Jean‐Paul - Abstract:
- Abstract: This paper contains the detailed synthesis and characterization protocols of ortho‐ functionalized tetrachlorinated azobenzene‐containing small interfering RNAs (siRNAs), which have photoswitchable properties effectively controlled with visible light. To design this tetrachlorinated azobenzene scaffold, a late‐stage chlorination with N ‐chlorosuccinimide and palladium is used. Next, a single hydroxyl group from the tetrachlorinated azobenzene is protected with a 4, 4′‐dimethoxytrityl (DMT) group, followed by phosphitylation with 2‐cyanoethyl‐ N, N ‐diisopropylchlorophosphoramidite. These phosphoramidite monomers are compatible with automated solid‐phase oligonucleotide synthesis to generate tetrachlorinated azobenzene‐containing oligonucleotides. This paper also contains the detailed biophysical characterization, biological testing, and photo‐switching protocols of ortho ‐functionalized chlorinated azobenzene‐containing siRNAs (Cl‐siRNAzos), which have photoswitchable properties that can be controlled with visible light. First, the Cl‐siRNAzos are characterized by annealing the sense and antisense strands together and then measuring the circular dichroism (CD) profile, and the melting temperatures ( T m ) of the duplexes. Secondly, the biological testing of the Cl‐siRNAzos in cell culture is done to determine their gene silencing efficacy. Finally, their gene‐silencing activities are measured after exposure to red light in order to inactivate the Cl‐siRNAzo, andAbstract: This paper contains the detailed synthesis and characterization protocols of ortho‐ functionalized tetrachlorinated azobenzene‐containing small interfering RNAs (siRNAs), which have photoswitchable properties effectively controlled with visible light. To design this tetrachlorinated azobenzene scaffold, a late‐stage chlorination with N ‐chlorosuccinimide and palladium is used. Next, a single hydroxyl group from the tetrachlorinated azobenzene is protected with a 4, 4′‐dimethoxytrityl (DMT) group, followed by phosphitylation with 2‐cyanoethyl‐ N, N ‐diisopropylchlorophosphoramidite. These phosphoramidite monomers are compatible with automated solid‐phase oligonucleotide synthesis to generate tetrachlorinated azobenzene‐containing oligonucleotides. This paper also contains the detailed biophysical characterization, biological testing, and photo‐switching protocols of ortho ‐functionalized chlorinated azobenzene‐containing siRNAs (Cl‐siRNAzos), which have photoswitchable properties that can be controlled with visible light. First, the Cl‐siRNAzos are characterized by annealing the sense and antisense strands together and then measuring the circular dichroism (CD) profile, and the melting temperatures ( T m ) of the duplexes. Secondly, the biological testing of the Cl‐siRNAzos in cell culture is done to determine their gene silencing efficacy. Finally, their gene‐silencing activities are measured after exposure to red light in order to inactivate the Cl‐siRNAzo, and then either violet light or infrared thermal relaxation is deployed, which re‐activates the Cl‐siRNAzo. © 2022 Wiley Periodicals LLC. Basic Protocol 1 : Synthesis of 4, 4′‐bis(hydroxyethyl) ortho‐ functionalized tetrachlorinated azobenzene phosphoramidite (5 ) Basic Protocol 2 : Synthesis, purification, and characterization of siRNAs containing ortho‐ functionalized tetrachlorinated azobenzene Basic Protocol 3 : Gene‐silencing evaluation of ortho‐ functionalized tetrachlorinated azobenzene using firefly luciferase … (more)
- Is Part Of:
- Current protocols. Volume 2:Issue 8(2022)
- Journal:
- Current protocols
- Issue:
- Volume 2:Issue 8(2022)
- Issue Display:
- Volume 2, Issue 8 (2022)
- Year:
- 2022
- Volume:
- 2
- Issue:
- 8
- Issue Sort Value:
- 2022-0002-0008-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-08-23
- Subjects:
- azobenzene -- oligonucleotide -- phosphoramidite -- photochemistry -- photocontrolled gene silencing -- siRNAzos
Life sciences -- Laboratory manuals -- Periodicals
Biology -- Laboratory manuals -- Periodicals
Life sciences -- Technique -- Periodicals
Biology -- Technique -- Periodicals
570.028 - Journal URLs:
- https://currentprotocols.onlinelibrary.wiley.com/journal/26911299 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cpz1.513 ↗
- Languages:
- English
- ISSNs:
- 2691-1299
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23128.xml