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公开(公告)号:US20220282294A1
公开(公告)日:2022-09-08
申请号:US17631407
申请日:2020-07-31
Applicant: Japan Science and Technology Agency
Inventor: Hiroshi Abe , Naoko Abe , Kosuke Nakamoto , Hiroki Murase , Yasuaki Kimura
Abstract: A primer for amplifying a nucleic acid having a structure represented by the formula (1): where B represents a base, R1 represents a decomposable protecting group, and R2 represents hydrogen or a hydroxyl group, and the symbol * represents a bond to a sugar of an adjacent nucleotide. A device for producing double-stranded DNA, includes: a forward primer and a reverse primer, having a structure represented by formula (1); a PCR device for forming double-stranded DNA with 3′-recessed ends by performing multiple cycles of PCR by using a template DNA as a template; and a photoirradiation unit for deprotecting R1 and forming a sticky end with a 3′-protruding end.
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2.
公开(公告)号:US20230193294A1
公开(公告)日:2023-06-22
申请号:US17768942
申请日:2020-10-05
Applicant: Japan Science and Technology Agency
Inventor: Hiroshi Abe , Naoko Abe
Abstract: A mRNA for the synthesis of a protein, including a translation region containing a start codon and a stop codon and an untranslated region positioned on the 5′-end side of the start codon, in which some phosphate groups within the range of at least from the 5′end of the untranslated region to 15 nt on the 3′-end side of the start codon are substituted with phosphorothioate groups, is provided. A method for producing an mRNA, including: a step of preparing a DNA template; a step of preparing an unmodified NTP containing ATP, GTP, CTP, and UTP, and a modified NTP in which at least one kind of phosphate group of the unmodified NTP is substituted with a phosphorothioate group; and a step of performing a transcription reaction with RNA polymerase using the DNA template as a template and the unmodified NTP and the modified NTP as substrates, is also provided.
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公开(公告)号:US20250163098A1
公开(公告)日:2025-05-22
申请号:US18696694
申请日:2022-09-27
Applicant: Japan Science and Technology Agency
Inventor: Hiroshi Abe , Masahito Inagaki , Fumitaka Hashiya , Haruka Hiraoka , Naoko Abe
IPC: C07H21/04
Abstract: There is provided a nucleic acid strand cleaving method including a nucleic acid preparation step of preparing a nucleic acid to be cleaved having a structure represented by the following Formula (1), and a cleaving step of reacting the nucleic acid to be cleaved with a cleaving agent to cleave the nucleic acid to be cleaved at the part X of the Formula (1) to generate a nucleic acid having a structure represented by the following Formula (2). The cleaving agent is a metal nanoparticle containing an atom selected from the group consisting of silver, mercury, and cadmium. [Chemical Formula 1] Here, B represents a base, and X represents sulfur or selenium. NucA is composed of at least one nucleotide and is a part of the nucleic acid to be cleaved, and represents a part on the 5′ end side with reference to the X. NucB is composed of at least one nucleotide and is a part of the nucleic acid to be cleaved, and represents a part on the 3′ end side with reference to the X.
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4.
公开(公告)号:US20240327444A1
公开(公告)日:2024-10-03
申请号:US18576587
申请日:2022-07-05
Applicant: Japan Science and Technology Agency , National University Corporatjion Tokai National Higher Education and Research System
Inventor: Hiroshi Abe , Naoko Abe , Masahito Inagaki , Yasuaki Kimura , Fumitaka Hashiya , Zhenmin Li , Yuko Nakashima
IPC: C07H1/06 , A61K31/7105 , C07F9/24 , C07H17/02 , C07H21/00
CPC classification number: C07H1/06 , A61K31/7105 , C07F9/2458 , C07H17/02 , C07H21/00
Abstract: A method for purifying a nucleotide-based substance; including a protecting group introduction step of introducing a hydrophobic protecting group represented by the following formula (P1) or (P2) into a nucleotide-based substance to produce a hydrophobic nucleotide-based substance; an isolation and purification step of isolating and purifying the hydrophobic nucleotide-based substance under a hydrophobic environment; and a deprotection step of deprotecting the hydrophobic protecting group from the hydrophobic nucleotide-based substance to produce the nucleotide-based substance,
wherein R1 represents a linear or branched alkyl group having 1 to 30 carbon atoms, R4 represents hydrogen or a linear or branched alkyl group having 1 to 10 carbon atoms, R2, R3, R5 and R6 represent hydrogen, a linear or branched alkyl group having 1 to 10 carbon atoms, or the like, and may be the same or different; and * means a bond with a nucleotide-based substance.-
公开(公告)号:US20230097172A1
公开(公告)日:2023-03-30
申请号:US17802680
申请日:2021-02-19
Applicant: Japan Science and Technology Agency
Inventor: Hiroshi Abe , Yasuaki Kimura , Naoko Abe
Abstract: A method for producing a capped RNA which is an RNA having the 5′-end modified with a cap, the method including: reacting an activated capping compound represented by with a monophosphate RNA having the 5′-end monophosphorylated, where, L represents a leaving group. The activated capping compound is preferably a compound represented by
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公开(公告)号:US20220290232A1
公开(公告)日:2022-09-15
申请号:US17631418
申请日:2020-07-31
Applicant: Japan Science and Technology Agency
Inventor: Hiroshi Abe , Naoko Abe , Kosuke Nakamoto , Hiroki Murase , Yasuaki Kimura
IPC: C12Q1/6876
Abstract: A primer for amplifying a nucleic acid having a structure represented by formula (1): where A1 represents —S—, —S—S—, or —Se—, B represents a base, and R1 represents a decomposable protecting group, and the symbol * represents a bond to a sugar of an adjacent nucleotide. A device for producing double-stranded DNA includes: a forward primer and a reverse primer, having a structure represented by formula (1); a PCR device for forming double-stranded DNA with 3′-recessed ends by performing multiple cycles of PCR by using a template DNA as a template; Klenow fragment for making the 3′ ends blunt; and a photoirradiation unit for deprotecting R1 and forming a sticky end with a 3′-protruding end.
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