Rna-nanostructured double robots and methods of use thereof
AssigneeArizona Board of Regents on behalf of Arizona State University
InventorsYung CHANG, Hao YAN, Xiaodong QI, Fei ZHANG
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Abstract
Described herein are immuno-stimulatory RNA nanostructures (which comprises a single-stranded RNA (ssRNA) molecule, wherein the ssRNA molecule forms at least one paranemic cohesion crossover), as well as compositions and methods of use thereof.
Claims20
-51. (canceled)
A method of inhibiting tumor growth in a human subject, comprising administering to the subject a therapeutically effective amount of the composition comprising:
- an RNA nanostructure robot having the sequence of (R3)n—NR1-L-NR2—(R4)m, wherein:
- NR1 and NR2 independently represent an RNA nanostructure each comprising a nucleic acid sequence having at least about 90% sequence identity to SEQ ID NO:1 or SEQ ID NO:
- 9 that self-assembles into respective first and second scaffolds;
- L is a linker which operably links NR1 to NR2;
- wherein R3 and R4 are independently selected from a pair of fastener strands, an aptamer, a cargo molecule, a capture strand, a targeting strand, and H;
- n is an integer from 1 to 20;
- and
- m is an integer from 0 to 20,
- and a pharmaceutically acceptable carrier.
A method of inducing a tumor necrosis response in a human subject, comprising administering to the subject a therapeutically effective amount of the composition comprising:
- an RNA nanostructure robot having the sequence of (R3)n—NR1-L-NR2—(R4)m, wherein:
- NR1 and NR2 independently represent an RNA nanostructure each comprising a nucleic acid sequence having at least about 90% sequence identity to SEQ ID NO:1 or SEQ ID NO:
- 9 that self-assembles into respective first and second scaffolds;
- L is a linker which operably links NR1 to NR2;
- Preliminary Amendment dated Jan. 24, 2022 wherein R3 and R4 are independently selected from a pair of fastener strands, an aptamer, a cargo molecule, a capture strand, a targeting strand, and H;
- n is an integer from 1 to 20;
- and
- m is an integer from 0 to 20,
- and a pharmaceutically acceptable carrier.
A method for the prophylactic or therapeutic treatment of cancer in a human subject, comprising administering to the subject a therapeutically effective amount of the composition comprising:
- an RNA nanostructure robot having the sequence of (R3)n—NR1-L-NR2—(R4)m, wherein:
- NR1 and NR2 independently represent an RNA nanostructure each comprising a nucleic acid sequence having at least about 90% sequence identity to SEQ ID NO:1 or SEQ ID NO:
- 9 that self-assembles into respective first and second scaffolds;
- L is a linker which operably links NR1 to NR2;
- wherein R3 and R4 are independently selected from a pair of fastener strands, an aptamer, a cargo molecule, a capture strand, a targeting strand, and H;
- n is an integer from 1 to 20;
- and
- m is an integer from 0 to 20,
- and a pharmaceutically acceptable carrier.
A method of activating or stimulating the immune system by triggering the toll-like receptor 3 (TLR3) signaling pathway in a human subject, the method comprising administering to the subject a therapeutically effective amount of the composition comprising:
- an RNA nanostructure robot having the sequence of (R3)n—NR1-L-NR2—(R4)m, wherein:
- NR1 and NR2 independently represent an RNA nanostructure each comprising a nucleic acid sequence having at least about 90% sequence identity to SEQ ID NO:1 or SEQ ID NO:
- 9 that self-assembles into respective first and second scaffolds;
- L is a linker which operably links NR1 to NR2;
- wherein R3 and R4 are independently selected from a pair of fastener strands, an aptamer, a cargo molecule, a capture strand, a targeting strand, and H;
- n is an integer from 1 to 20;
- and
- m is an integer from 0 to 20,
- and a pharmaceutically acceptable carrier.
Dependencies are inferred from the claim text.