Method, composition and device for sampling natriuretic peptides in a biological fluid
Disclosed is a composition that synergistically prevents proteolysis or modification of peptides in sampled biological fluids using sulfonyl fluoride family protease inhibitors at high concentrations combined with at least one additional protease inhibitor of a different type, preferably a broad spectrum protease inhibitor, and a chelator. A preferred embodiment uses AEBSF at 10 mM, Benzamidine at 20 mM and EDTA as the chelator. The disclosed composition may be combined with other protease inhibitors to further modulate its specificity, for instance to additionally target acidic proteases. Additional protease inhibitors, reducing agents, stabilizers and buffering agents may be combined with the disclosed compositions in devices for sampling or testing biological fluids for levels of peptides of interest, or methods therefore. The disclosed devices, compositions and methods are of particular use in sampling and testing for the level of natriuretic peptides.
1. A composition comprising a mixture of:
(a) a first protease inhibitor selected from the group consisting of leupeptin and benzamidine;
(b) a second protease inhibitor that is 4-(2-aminoethyl)benzenesulfonyl fluoride hydrochloride (AEBSF), wherein the second protease inhibitor does not inhibit formation of protein adducts in a peptide in the absence of the first protease inhibitor; and
(c) a peptide;
wherein an effective concentration of the first protease inhibitor and the second protease inhibitor is a concentration effective to inhibit proteolysis of the peptide while not inducing formation of adducts of the peptide when combined, and
wherein the effective concentration comprises:
(i) about 20 mM benzamidine and about 10 mM AEBSF, or
(ii) about 2.5 mM leupeptin and about 2.5 mM AEBSF.
2. The composition according to claim 1 , wherein the composition is stable for at least one of (i) two hours at room temperature, and (ii) at least six months at −70° C.
3. The composition according to claim 1 , further comprising a chelator.
4. The composition according to claim 3 , wherein the chelator is ethylenediaminetetraacetic acid.
5. The composition according to claim 4 , wherein the ethylenediaminetetraacetic acid is present in the composition at a concentration of at least about 1 mM.
6. A device comprising a tube and a cap, wherein the device is capable of holding a biological fluid sample, wherein the device has disposed therein:
(a) a first protease inhibitor selected from the group consisting of leupeptin and benzamidine; and
(b) a second protease inhibitor that is 4-(2-aminoethyl)benzenesulfonyl fluoride hydrochloride (AEBSF);
wherein the device has disposed therein sufficient protease inhibitor to be at a concentration of:
(i) about 20 mM benzamidine and about 10 mM AEBSF, or
(ii) about 2.5 mM leupeptin and about 2.5 mM AEBSF, when diluted by the biological fluid sample.
7. The device according to claim 6 , further comprising at least one stabilizer or buffer.
8. The device according to claim 6 , further comprising a chelator.
9. The device according to claim 8 , wherein the chelator is ethylenediaminetetraacetic acid.
10. The device according to claim 6 , further comprising heparin.
11. The device according to claim 6 , wherein the device has disposed therein about 10 mM AEBSF and about 20 mM benzamidine.
12. The device according to claim 6 , wherein the device has disposed therein about 2.5 mM leupeptin and about 2.5 mM AEBSF.
13. A blood collection tube capable of holding a blood sample, wherein the blood collection tube has disposed therein:
(a) a first protease inhibitor selected from the group consisting of leupeptin and benzamidine; and
(b) a second protease inhibitor that is 4-(2-aminoethyl)benzenesulfonyl fluoride hydrochloride (AEBSF);
wherein the blood collection tube has disposed therein sufficient protease inhibitor to be at a concentration of:
(i) about 20 mM benzamidine and about 10 mM AEBSF, or
(ii) about 2.5 mM leupeptin and about 2.5 mM AEBSF, when diluted by the blood sample.
14. The blood collection tube according to claim 13 , further comprising at least one stabilizer or buffer.
15. The blood collection tube according to claim 13 , further comprising a chelator.
16. The blood collection tube according to claim 13 , wherein the chelator is ethylenediaminetetraacetic acid.
17. The blood collection tube according to claim 13 , further comprising heparin.
18. The blood collection tube according to claim 13 , wherein the blood collection tube has disposed therein about 10 mM AEBSF and about 20 mM benzamidine.
19. The blood collection tube according to claim 13 , wherein the blood collection tube has disposed therein about 2.5 mM leupeptin and about 2.5 mM AEBSF.