US2003032094A1PendingUtilityA1
Isolated mammalian dendritic cell genes; related reagents
Priority: Nov 27, 1996Filed: Nov 27, 2001Published: Feb 13, 2003
Est. expiryNov 27, 2016(expired)· nominal 20-yr term from priority
Inventors:Elizabeth BatesBlandine Marie De Saint-VisChristophe CauxSerge LebecqueJacques F. Banchereau
C07K 2319/00Y10S435/975C07K 14/70503
49
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Claims
Abstract
Nucleic acids encoding various dendritic cell specific proteins from a primate, reagents related thereto, including specific antibodies, and purified proteins are described. Methods of using said reagents and related diagnostic kits are also provided.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A composition of matter selected from the group consisting of:
a) a substantially pure or recombinant A05F12 protein or peptide exhibiting at least about 85% sequence identity over a length of at least about 12 amino acids to SEQ ID NO: 2 or 4; b) a natural sequence A05F12 comprising SEQ ID NO: 2 or 4; c) a fusion protein comprising A05F12 sequence; d) a substantially pure or recombinant A07C03 protein or peptide exhibiting at least about 85% sequence identity over a length of at least about 12 amino acids to SEQ ID NO: 6, 8, or 10; e) a natural sequence A07C03 comprising SEQ ID NO: 6, 8, or 10; f) a fusion protein comprising A07C03 sequence; g) a substantially pure or recombinant E02B02 protein or peptide exhibiting at least about 85% sequence identity over a length of at least about 12 amino acids to SEQ ID NO: 12; h) a natural sequence E02B02 comprising SEQ ID NO: 12; and i) a fusion protein comprising E02B02 sequence.
2 . A substantially pure or isolated protein comprising a segment exhibiting sequence identity to a corresponding portion of an:
a) A05F12 of claim 1 , wherein:
i) said homology is at least about 90% identity and said portion is at least about 9 amino acids;
ii) said homology is at least about 80% identity and said portion is at least about 17 amino acids; or
iii) said homology is at least about 70% identity and said portion is at least about 25 amino acids;
b) A07C03 of claim 1 , wherein:
i) said homology is at least about 90% identity and said portion is at least about 9 amino acids;
ii) said homology is at least about 80% identity and said portion is at least about 17 amino acids; or
iii) said homology is at least about 70% identity and said portion is at least about 25 amino acids; or
c) E02B02 of claim 1 , wherein:
i) said homology is at least about 90% identity and said portion is at least about 9 amino acids;
ii) said homology is at least about 80% identity and said portion is at least about 17 amino acids; or
iii) said homology is at least about 70% identity and said portion is at least about 25 amino acids.
3 . The composition of matter of claim 1 , wherein said:
a) A05F12 comprises a mature sequence of Table 1; b) A05F12 protein or peptide:
i) is from a warm blooded animal selected from a primate or rodent, such as a human or mouse;
ii) comprises at least one polypeptide segment of SEQ ID NO: 2 or 4;
iii) exhibits a plurality of portions exhibiting said identity;
iv) is a natural allelic variant of a primate or rodent A05F12;
v) has a length at least about 30 amino acids;
vi) exhibits at least two non-overlapping epitopes which are specific for a primate or rodent A05F12;
vii) exhibits a sequence identity at least about 90% over a length of at least about 20 amino acids to a primate or rodent A05F12;
viii) has a molecular weight of at least 100 kD with natural glycosylation;
ix) is a synthetic polypeptide;
x) is attached to a solid substrate;
xi) is conjugated to another chemical moiety;
xii) is a 5-fold or less substitution from natural sequence; or
xiii) is a deletion or insertion variant from a natural sequence;
c) A07C03 comprises a mature sequence of Table 2; d) A07C03 protein or peptide:
i) is from a warm blooded animal selected from a primate or rodent, such as a human or mouse;
ii) comprises at least one polypeptide segment of SEQ ID NO: 8 or 10;
iii) exhibits a plurality of portions exhibiting said identity;
iv) is a natural allelic variant of a primate or rodent A07C03;
v) has a length at least about 30 amino acids;
vi) exhibits at least two non-overlapping epitopes which are specific for a primate or rodent A07C03;
vii) exhibits a sequence identity at least about 90% over a length of at least about 20 amino acids to a primate or rodent A07C03;
viii) has a molecular weight of at least 100 kD with natural glycosylation;
ix) is a synthetic polypeptide;
x) is attached to a solid substrate;
xi) is conjugated to another chemical moiety;
xii) is a 5-fold or less substitution from natural sequence; or
xiii) is a deletion or insertion variant from a natural sequence;
e) E02B02 comprises a mature sequence of Table 3; or f) E02B02 protein or peptide:
i) is from a warm blooded animal selected from a primate, such as a human;
ii) comprises at least one polypeptide segment of SEQ ID NO: 12;
iii) exhibits a plurality of portions exhibiting said identity;
iv) is a natural allelic variant of a primate E02B02;
v) has a length at least about 30 amino acids;
vi) exhibits at least two non-overlapping epitopes which are specific for a primate E02B02;
vii) exhibits a sequence identity at least about 90% over a length of at least about 20 amino acids to a primate oE02B02;
viii) has a molecular weight of at least 100 kD with natural glycosylation;
ix) is a synthetic polypeptide;
x) is attached to a solid substrate;
xi) is conjugated to another chemical moiety;
xii) is a 5-fold or less substitution from natural sequence; or
xiii) is a deletion or insertion variant from a natural sequence.
4 . A composition comprising:
a) a sterile A05F12 protein or peptide of claim 1; b) said A05F12 protein or peptide of claim 1 and a carrier, wherein said carrier is:
i) an aqueous compound, including water, saline, and/or buffer; and/or
ii) formulated for oral, rectal, nasal, topical, or parenteral administration;
c) a sterile A07C03 protein or peptide of claim 1; d) said A07C03 protein or peptide of claim 1 and a carrier, wherein said carrier is:
i) an aqueous compound, including water, saline, and/or buffer; and/or
ii) formulated for oral, rectal, nasal, topical, or parenteral administration;
e) a sterile E02B02 protein or peptide of claim 1; or f) said E02B02 protein or peptide of claim 1 and a carrier, wherein said carrier is:
i) an aqueous compound, including water, saline, and/or buffer; and/or
ii) formulated for oral, rectal, nasal, topical, or parenteral administration.
5 . The fusion protein of claim 1 , comprising:
a) mature protein sequence of Table 1, 2, or 3; b) a detection or purification tag, including a FLAG, His6, or Ig sequence; or c) sequence of another receptor protein.
6 . A kit comprising a protein or polypeptide of claim 1 , and:
a) a compartment comprising said protein or polypeptide; and/or b) instructions for use or disposal of reagents in said kit.
7 . A binding compound comprising an antigen binding site from an antibody, which specifically binds to a natural:
A) A05F12 protein of claim 1 , wherein:
a) said protein is a primate or rodent protein;
b) said binding compound is an Fv, Fab, or Fab2 fragment;
c) said binding compound is conjugated to another chemical moiety; or
d) said antibody:
i) is raised against a peptide sequence of a mature polypeptide of Table 1;
ii) is raised against a mature primate or rodent A05F12;
iii) is raised to a purified human A05F12;
iv) is raised to a purified mouse A05F12;
v) is immunoselected;
vi) is a polyclonal antibody;
vii) binds to a denatured A05F12;
viii) exhibits a Kd to antigen of at least 30 μM;
ix) is attached to a solid substrate, including a bead or plastic membrane;
x) is in a sterile composition; or
xi) is deteccably labeled, including a radioactive or fluorescent label;
B) A07C03 protein of claim 1 , wherein:
a) said protein is a primate or rodent protein;
b) said binding compound is an Fv, Fab, or Fab2 fragment;
c) said binding compound is conjugated to another chemical moiety; or
d) said antibody:
i) is raised against a peptide sequence of a mature polypeptide of Table 2;
ii) is raised against a mature primate or rodent A07C03;
iii) is raised to a purified human A07C03;
iv) is raised to a purified mouse A07C03;
v) is immunoselected;
vi) is a polyclonal antibody;
vii) binds to a denatured A07C03;
viii) exhibits a Kd to antigen of at least 30 μM;
ix) is attached to a solid substrate, including a bead or plastic membrane;
x) is in a sterile composition; or
xi) is detectably labeled, including a radioactive or fluorescent label; or
C) E02B02 protein of claim 1 , wherein:
a) said protein is a primate protein;
b) said binding compound is an Fv, Fab, or Fab2 fragment;
c) said binding compound is conjugated to another chemical moiety; or
d) said antibody:
i) is raised against a peptide sequence of a mature polypeptide of Table 3;
ii) is raised against a mature primate E02B02;
iii) is raised to a purified human E02B02;
iv) is immunoselected;
v) is a polyclonal antibody;
vi) binds to a denatured E02B02;
vii) exhibits a Kd to antigen of at least 30 μM;
viii) is attached to a solid substrate, including a bead or plastic membrane;
ix) is in a sterile composition; or
x) is detectably labeled, including a radioactive or fluorescent label
8 . A kit comprising said binding compound of claim 7 , and:
a) a compartment comprising said binding compound; and/or b) instructions for use or disposal of reagents in said kit.
9 . The kit of claim 8 capable of making a qualitative or quantitative analysis.
10 . A composition comprising:
a) a sterile binding compound of claim 7; or b) said binding compound of claim 7 and a carrier, wherein said carrier is:
i) an aqueous compound, including water, saline, and/or buffer; and/or
ii) formulated for oral, rectal, nasal, topical, or parenteral administration.
11 . An isolated or recombinant nucleic acid encoding a protein or peptide or fusion protein of claim 1 , wherein:
a) said A05F12 protein or peptide is from a mammal, including a primate or rodent; b) said nucleic acid:
i) encodes an antigenic peptide sequence of Table 1;
ii) encodes a plurality of antigenic peptide sequences of Table 1;
iii) exhibits at least about 80% identity to a natural cDNA encoding said segment;
iv) is an expression vector;
v) further comprises an origin of replication;
vi) is from a natural source;
vii) comprises a detectable label;
viii) comprises synthetic nucleotide sequence;
ix) is less than 6 kb, preferably less than 3 kb;
x) is from a mammal, including a primate or rodent;
xi) comprises a natural full length coding sequence;
xii) is a hybridization probe for a gene encoding said A05F12; or
xiii) is a PCR primer, PCR product, or mutagenesis primer;
c) said A05C03 is from a mammal, including a primate or rodent; d) said nucleic acid:
i) encodes an antigenic peptide sequence of Table 2;
ii) encodes a plurality of antigenic peptide sequences of Table 2;
iii) exhibits at least about 80% identity to a natural cDNA encoding said segment;
iv) is an expression vector;
v) further comprises an origin of replication;
vi) is from a natural source;
vii) comprises a detectable label;
viii) comprises synthetic nucleotide sequence;
ix) is less than 6 kb, preferably less than 3 kb;
x) is from a mammal, including a primate or rodent;
xi) comprises a natural full length coding sequence;
xii) is a hybridization probe for a gene encoding said A07C03; or
xiii) is a PCR primer, PCR product, or mutagenesis primer;
e) said E02B02 is from a mammal, including a primate; or f) said nucleic acid:
i) encodes an antigenic peptide sequence of Table 3;
ii) encodes a plurality of antigenic peptide sequences of Table 3;
iii) exhibits at least about 80% identity to a natural cDNA encoding said segment;
iv) is an expression vector;
v) further comprises an origin of replication;
vi) is from a natural source;
vii) comprises a detectable label;
15 . The kit of claim 14 capable of making a qualitative or quantitative analysis.
16 . A nucleic acid which:
a) hybridizes under wash conditions of 30° C. and less than 2M salt to SEQ ID NO: 1 or 3; b) exhibits at least about 85% identity over a stretch of at least about 30 nucleotides to a primate or rodent A05F12; c) hybridizes under wash conditions of 30° C. and less than 2M salt to SEQ ID NO: 5, 7, or 9; d) exhibits at least about 85% identity over a stretch of at least about 30 nucleotides to a primate or rodent A07C03; e) hybridizes under wash conditions of 30° C. and less than 2M salt to SEQ ID NO: 11; or b) exhibits at least about 85% identity over a stretch of at least about 30 nucleotides to a primate E02B02.
17 . The nucleic acid of claim 16 , wherein:
a) said wash conditions are at 45° C. and/or 500 mM salt; or b) said identity is at least 90% and/or said stretch is at least 55 nucleotides.
18 . The nucleic acid of claim 17 , wherein:
a) said wash conditions are at 55° C. and/or 150 mM salt; or b) said identity is at least 95% and/or said stretch is at least 75 nucleotides.
19 . A method of modulating physiology or development of a cell or tissue culture cells comprising contacting said cell with:
a) a binding composition of claim 7 , which binds to a primate or rodent A05F12; b) a binding composition of claim 7 , which binds to a primate or rodent A07C03; c) a binding composition of claim 7 , which binds to a primate E01B02; d) a antisense nucleic acid which blocks expression of a primate or rodent A05F12; e) a antisense nucleic acid which blocks expression of a primate or rodent A07C03; or f) a antisense nucleic acid which blocks expression of a primate E02B02.Join the waitlist — get patent alerts
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