A novel affinity peptide library of igg constructed based on protein a affinity model and the application of the design method thereof
US-2015355192-A1 · Dec 10, 2015 · US
US9953131B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9953131-B2 |
| Application number | US-201615273094-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 22, 2016 |
| Priority date | Jan 29, 2007 |
| Publication date | Apr 24, 2018 |
| Grant date | Apr 24, 2018 |
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The present invention relates to novel short interfering RNA (siRNA) molecules that are multi-targeted. More specifically, the present invention relates to siRNA molecules that target two or more sequences. In one embodiment, multi-targeting siRNA molecules are designed to incorporate features of siRNA molecules and features of micro-RNA (miRNA) molecules. In another embodiment, multi-targeting siRNA molecules are designed so that each strand is directed to separate targets.
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What is claimed is: 1. A method for designing a multi-targeting RNA molecule comprising: (a) selecting one mRNA and one 3′ UTR target sequence; (b) identifying all 19mer siRNA candidates that have perfect complementarity to the mRNA; (c) identifying effective cleavage target sites within the mRNA with an siRNA efficacy prediction algorithm; and (d) ordering the siRNA candidates based on predicted miRNA-like down-regulation; wherein the multi-targeting RNA molecule targets both the mRNA and the 3′ UTR target sequences. 2. The method of claim 1 , wherein the predicted miRNA-like down-regulation is based on the number of and distance between miRNA-like target sites within the 3′ UTR. 3. The method of claim 1 which further comprises (b′) identifying miRNA-like target sites within the 3′ UTR for each siRNA candidate and removing candidates that have no miRNA-like target sites. 4. The method of claim 2 which further comprises (b′) identifying miRNA-like target sites within the 3′ UTR for each siRNA candidate and removing candidates that have no miRNA-like target sites. 5. The method of claim 1 , wherein the multi-targeting RNA molecule has both siRNA and miRNA functions. 6. The method of claim 1 , wherein the multi-targeting RNA molecule comprises a first strand and a second strand, wherein the first strand targets the mRNA and the second strand targets the 3′ UTR target sequence.
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