Protease inhibitor conjugates and antibodies useful in immunoassay
View Patent ↗Activated haptens useful for generating immunogens to HIV protease inhibitors, immunogens useful for producing antibodies to HIV protease inhibitors, and antibodies and labeled conjugates useful in immunoassays for HIV protease inhibitors. The novel haptens feature an activated functionality at the central, non-terminal hydroxyl group common to all HIV protease inhibitors, e.g., saquinavir, nelfinavir, indinavir, amprenavir, ritonavir, lopinavir, and atazanavir.
1. A compound having the structure
wherein
A is an activated ester.
2. The compound of claim 1 wherein A is succinimido-oxycarbonyl.
3. The compound O c -(succinimido-oxycarbonyl-butyryl-aminocaproyl)-lopinavir.
4. The compound O c -[4′-(succinimido-oxycarbonyl)-benzoyl-aminocaproyl]-lopinavir.
5. A compound having the structure
wherein
Y is O, S, or NH,
m is 0 or 1,
L is a linker comprising 0 to 40 carbon atoms arranged in a straight chain or a branched chain, saturated or unsaturated, and further comprising up to two ring structures and 0–20 heteroatoms, with the proviso that not more than two heteroatoms are linked in sequence, Z is a moiety selected from the group consisting of —CONH—, —NHCO—, —NHCONH—, —NHCSNH—, —OCONH—, —NHOCO—, —S—, —NH(C═NH)—, —N═N—, —NH—, and
P is selected from the group consisting of polypeptides, polysaccharides and synthetic polymers, and
n is a number from 1 to 50 per 50 kilodaltons molecular weight of P.
6. The compound of claim 5 wherein P is an aminated dextran.
7. The compound of claim 5 wherein P is bovine serum albumin.
8. The compound of claim 5 wherein P is keyhole limpet hemocyanin.
9. The compound of claim 5 wherein P is Limulus polyphemus hemocyanin.
10. The compound of claim 5 wherein P is bovine thyroglobulin.
11. The compound O c -(succinimido-oxycarbonyl-butyryl-aminocaproyl)-lopinavir conjugate with KLH.
12. The compound O c -[4′-(succinimido-oxycarbonyl)-benzoyl-aminocaproyl]-lopinavir conjugate with BSA.
13. A compound having the structure
wherein
Y is O, S, or NH,
m is 0 or 1,
L is a linker comprising 0 to 40 carbon atoms arranged in a straight chain or a branched chain, saturated or unsaturated, and further comprising up to two ring structures and 0–20 heteroatoms, with the proviso that not more than two heteroatoms are linked in sequence,
Z is a moiety selected from the group consisting of —CONH—, —NHCO—, —NHCONH—, —NHCSNH—, —OCONH—, —NHOCO—, —S—, —NH(C═NH)—, —N═N—, —NH—, and
Q is selected from the group consisting of non-isotopic labels,
and n is a number from 1 to 50 per 50 kilodaltons molecular weight of Q.
14. The compound of claim 13 wherein Q is biotin.
15. The compound O c -[4′-(1-biotinyl-amino-3,6-dioxa-octylamino)-terephthaloyl-aminocaproyl]-lopinavir.
16. An antibody generated in response to a compound having the structure:
wherein
Y is O, S, or NH,
m is 0 or 1,
L is a linker comprising 0 to 40 carbon atoms arranged in a straight chain or a branched chain, saturated or unsaturated, and further comprising up to two ring structures and 0–20 heteroatoms, with the proviso that not more than two heteroatoms are linked in sequence,
Z is a moiety selected from the group consisting of —CONH—, —NHCO—, —NHCONH—, —NHCSNH—, —OCONH—, —NHOCO—, —S—, —NH(C═NH)—, —N═N—, —NH—, and
P is selected from the group consisting of polypeptides, a polysaccharides, and synthetic polymers,
and n is a number from 1 to 50 per 50 kilodaltons molecular weight of P.
17. An antibody generated in response to the compound of claim 11 .
18. A compound having the structure
wherein
Y is O,
m is 1,
L is a linker comprising from 1 to 40 carbon atoms arranged in a straight chain or a branched chain, saturated or unsaturated, and containing up to two ring structures and 0–20 heteroatoms, with the proviso that not more than two heteroatoms may be linked in sequence, and
A is an activated ester.
19. The compound of claim 18 wherein A is succinimido-oxycarbonyl.