US2003166286A1PendingUtilityA1
Chimeric adenoviral fiber protein and methods of using same
Est. expiryFeb 21, 2015(expired)· nominal 20-yr term from priority
Inventors:Thomas WickhamErik Falck-PedersenPetrus W. RoelvinkJoseph T. BruderJason G. D. GallImre Kovesdi
A61K 48/00C07K 14/005C07K 2319/00C12N 2710/10345C12N 2710/10343C12N 2810/6018C12N 2710/10322C12N 2810/405C12N 15/86C12N 2830/60C12N 2830/00
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Claims
Abstract
A recombinant adenovirus comprising a chimeric adenoviral fiber protein comprising a non-adenoviral amino acid sequence in place of or in addition to a native fiber amino acid sequence, wherein the chimeric adenoviral fiber protein comprises a trimerization domain and the non-adenoviral amino acid sequence is of a size such that folding of the chimeric adenoviral fiber protein and assembly of a complex comprising the chimeric adenoviral fiber protein and a penton base is not impeded, and an adenoviral transfer vector for the generation of such a recombinant adenovirus are provided.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A recombinant adenovirus comprising a chimeric adenoviral fiber protein comprising a non-adenoviral amino acid sequence in place of or in addition to a native fiber amino acid sequence, wherein the chimeric adenoviral fiber protein comprises a trimerization domain and the non-adenoviral amino acid sequence is of a size such that folding of the chimeric adenoviral fiber protein and assembly of a complex comprising the chimeric adenoviral fiber protein and a penton base is not impeded.
2 . The recombinant adenovirus of claim 1 , wherein the non-adenoviral amino acid sequence in the chimeric adenoviral fiber protein is a protein binding sequence
3 . The recombinant adenovirus of claim 2 , wherein the protein binding sequence is selected from the group consisting of a bispecific protein binding sequence and a multispecific protein binding sequence.
4 . The recombinant adenovirus of claim 2 , wherein the non-adenoviral amino acid sequence is located at the C-terminus of the chimeric fiber protein.
5 . The recombinant adenovirus of claim 2 , which further comprises a chimeric coat protein comprising a nonnative amino acid sequence that is specific for binding to a protein.
6 . The recombinant adenovirus of claim 5 , wherein the chimeric coat protein is selected from the group consisting of a chimeric penton base and a chimeric hexon.
7 . The recombinant adenovirus of claim 1 , wherein a native fiber receptor binding sequence in the chimeric adenoviral fiber protein is inactive.
8 . A viral transfer vector comprising a chimeric adenoviral fiber protein comprising a non-adenoviral amino acid sequence in place of or in addition to a native fiber amino acid sequence, wherein the chimeric adenoviral fiber protein comprises a trimerization domain and the non-adenoviral amino acid sequence is of a size such that folding of the chimeric adenoviral fiber protein and assembly of a complex comprising the chimeric adenoviral fiber protein and a penton base is not impeded.
9 . The viral transfer vector of claim 8 , wherein the viral transfer vector is an adenoviral transfer vector.
10 . The viral transfer vector of claim 9 , wherein the non-adenoviral amino acid sequence in the chimeric fiber protein is a protein binding sequence.
11 . The viral transfer vector of claim 10 , wherein the protein binding sequence is selected from the group consisting of a bispecific protein binding sequence and a multispecific binding sequence.
12 . The viral transfer vector of claim 10 , wherein the non-adenoviral amino acid sequence is located at the C-terminus of the chimeric fiber protein.
13 . The viral transfer vector of claim 9 , wherein a native fiber receptor binding sequence in the chimeric adenoviral fiber protein is inactive.Cited by (0)
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