Synthetic peptides of type II collagen for cartilage resorption assays

Abstract

The claimed invention is peptides synthesized to match telopeptide components of type II collagen degradation products in synovial fluid and blood, selected from among LGPREKGPDP (SEQ ID NO 11), LGPREKGPDPLQ (SEQ ID NO 12), LGPREKGPDPLQY (SEQ ID NO 13), FAGLGPREKGPDP (SEQ ID NO 14), FAGLGPREKGPDPLQ (SEQ ID NO 15), FAGLGPREKGPDPLQY (SEQ ID NO 16), IDMSAFAGLGPREKGPDP (SEQ ID NO 17), IDMSAFAGLGPREKGPDPLQ (SEQ ID NO 18), IDMSAFAGLGPREKGPDPLQY (SEQ ID NO 19), and EKGPDPLQYMR (SEQ ID NO 20), which maybe useful as immunogens and antigens in cartilage resorption assays.

Description

FIELD OF THE INVENTION

The invention relates to assays for detecting cross-linked telopeptide analytes indicative of type II collagen (cartilage) resorption in vivo, and in particular provides immunoassays for measuring and distinguishing between resorption of non-mineralized cartilage and mineralized cartilage, and for measuring total cartilage resorption in vivo.

BACKGROUND OF THE INVENTION

Reference is made to the applicant's prior U.S. Pat. Nos. 4,973,666, 5,140,103, 5,300,434, 5,320,970, 5,817,755, and 5,702,909, which are incorporated by reference herein.

Immunoassays are known for detecting telopeptide analytes indicative of collagen resorption in vivo. Examples of such type I collagen assays for measuring bone resorption include: WO 89/04491 (Eyre); WO 89/12824 (Robins); WO 91/08478 (Eyre); EP 0505210 A2 (Risteli & Risteli); WO 92/21698 (Eyre); WO 94/03813 (Naser et al.); WO 94/14844 (Baylink); WO 95/04282 (Naser et al.); WO 95/08115 (Qvist & Bonde); WO 96/12193 (Bonde & Qvist); EP 0718309 A1 (Naser et al.); and WO 96/36645 (Eyre et al.).

Examples of type II collagen telopeptide assays for measuring cartilage resorption include WO 91/08478 (Eyre); WO 95/08115 (Qvist & Bonde); and WO 96/12193 (Bonde & Qvist).

Examples of type III collagen telopeptide assays include WO 88/08980 (Risteli & Risteli) and WO 91/08478 (Eyre).

The following patent disclosures are also of interest: U.S. Pat. No. 4,628,027 (Gay) discloses in vitro diagnostic methods using monoclonal antibodies against connective tissue proteins. U.S. Pat. No. 5,316,914 (Oshima et al.) discloses an enzyme sandwich immunoassay of human type III, IV, and VI collagens applicable to diagnosis of hepatic diseases. WO 94/14070 (Poole & Hollander) discloses an immunoassay for the measurement of collagen cleavage in cartilage. WO 94/18563 (Barrach et al.) discloses sandwich immunoassay methods for detecting type II collagen derived peptides associated with arthritis.

Of particular interest is the applicant's prior international publication, WO 91/0478, which discloses the following urinary resorption products of type II collagen

wherein the parentheses indicate optional amino acid residues, and the cross-linking residue depicted as Hyl-Hyl-Hyl is hydroxylysyl pyridinoline (HP), a natural 3-hydroxypyridinium residue present in mature collagen fibrils of various tissues. These analytes derive from the C-terminal cross-linked telopeptide domain of type II collagen and so are collectively referred to herein as “col2CTx”.

The present disclosure also adopts the one-letter symbol form of amino acid shorthand; thus, the Glu-Hyl-Gly-Pro-Asp-(Pro)-(Leu) telopeptide components of the analytes shown above are referred to hereinafter as EKGPD (SEQ ID NO:1), EKGPDP (SEQ ID NO:2), and EKGPDPL (SEQ ID NO:3). Furthermore, as used herein the symbol “K” represents either lysine, in the case of linear peptides, or a cross-linking 3-hydroxypyridinium residue selected from among hydroxylysyl pyridinoline (HP) and lysyl pyridinoline (LP).

The applicant and colleagues have also described col2CTx in recent abstracts:

Eyre et al., Bone Miner. Res. 11(S1): S413, 1996, describes cross-linked telopeptides from collagen types I, II, and III in human urine.

Atley et al., Arth. Rheum. 40(9S):584, 1997, reports that RS-130830, a selective inhibitor of collagenase-3, blocks the release of hydroxyproline and a metalloproteinase (MMP) specific neoepitope, col2CTx, from bovine cartilage exposed to IL- 1α.

Atley et al., Trans. Orthop. Res. Soc., New Orleans, 1998, reports matrix metalloproteinase-mediated release of immunoreactive telopeptides from cartilage type II collagen. The aim of this study was to evaluate whether an immunoassay based on a monoclonal antibody (mAb) 2B4, which recognizes a domain of the α1(II) C-telopeptide EKGPDP, measures MMP cleavage products in cartilage. The mAb 2B4 recognizes the in vitro product of matrilysin digestion AFAGLGPREKGPDP (SEQ ID NO:4) of synthetic peptide AFAGLGPREKGPDPLQYMRA (SEQ ID NO:5), but not AFAGLGPREKGPDPLQ (SEQ ID NO:6), AFAGLGPREKGPDPLQY (SEQ ID NO:7), LQYMRA (SEQ ID NO:8), or YMRA (SEQ ID NO:9). The authors also noted detection of mAb 2B4 immunoreactivity in synovial fluid, serum, and urine. They concluded that this 2B4 epitope has the potential to be a useful marker of type II collagen resorption in vivo.

Moskowitz et al., Amer. Coll. Rheum., San Diego, Calif. Nov. 8-12, 1998, reports that the type II collagen C-telopeptide 2B4 epitope is a marker for cartilage resorption in familial osteoarthrosis.

Eyre et al., Combined Orthopaedic Research Societies Meeting, Vittel, France, Sept. 28-30, 1998, discusses biochemical markers of bone and collagen degradation, including a cross-linked telopeptide product of type II collagen degradation in urine (col2CTx).

Atley et al., Combined Orthopaedic Research Societies Meeting, Hamamatsu, Japan, 1998, discusses collagen type II cross-linked telopeptides, a promising marker for cartilage degradation in arthritis.

In addition, monoclonal antibodies to the C-telopeptide of type II collagen as diagnostic markers for rheumatoid arthritis are reportedly under development at Osteometer Biotech A/S. BioWorld International, page 3, Dec. 3, 1997.

The entire disclosures of the prior scientific and patent publications cited in this patent application are incorporated by reference herein.

SUMMARY OF THE INVENTION

The invention provides improved assays for measuring type II collagen (cartilage) resorption in vivo. The subject immunoassays are useful for distinguishing between resorption of non-mineralized cartilage and mineralized cartilage, and for measuring total cartilage resorption in vivo. The disclosed immunoassays employ either one or a combination of two antibodies. A first antibody binds to DEKAGGA (SEQ ID NO:21) but not to GGFDEKAGGAQLG (SEQ ID NO:27), where the K symbols refer to lysine residues and/or preferably to cross-linking 3-hydroxypyridinium residues. Measurement of analyte binding to the first antibody in serum provides an indication of non-mineralized cartilage resorption in vivo.

A second antibody binds to GGFDEKAGGAQLG but not to DEKAGGA, where the K symbols also preferably refer to cross-linking 3-hydroxypyridinium residues. Measurement of analyte binding to the second antibody in serum provides an indication of mineralized cartilage resorption in vivo.

An indication of total (non-mineralized and mineralized) cartilage resorption in vivo is provided by either measurement of analyte binding to the first antibody in urine, or by measurement of the total analyte binding to the first and second antibodies in serum.

The subject cartilage markers are preferably measured in conjunction with bone collagen resorption markers selected from among amino-terminal telopeptides of type I collagen, carboxy-terminal telopeptides of type I collagen, and free lysyl pyridinoline (deoxypyridinoline) cross-links.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

By way of introduction, the monoclonal antibody 2B4 recognizes a C-terminal epitope in the sequence EKGPDP (SEQ ID NO;2). The antibody requires the C-terminal proline to be free for any binding (i.e., Pro-COOH) and prefers K to be derivatized (e.g., cross-linked) through its side-chain (epsilon) amino group. The presence of extra amino acids C-terminal to the proline prevents mAb 2B4 binding to this peptide domain.

Various matrix metalloproteinases (MMPs) including collagenases (MMP1 and MMP13), gelatinases (MMP2 and 9), stromelysin (MMP3), and matrilysin (MMP7) can generate the mAb 2B4 epitope from cartilage type II collagen or a synthetic C-telopeptide domain (AFAGLGPREKGPDPLQYMR (SEQ ID NO:5). Matrilysin (MMP7) is the most potent based on in vitro studies with the recombinant enzymes.

Cathepsin K, however, is unable to cleave the P-L bond required for 2B4 epitope release, but generates a longer fragment, EKGPDPLQ (SEQ ID NO:10). This is significant because cathepsin K is a protease expressed essentially only by osteoclasts and is the key enzyme responsible for the resorption of the calcified collagen when osteoclasts resorb bone. Osteoclasts (or a very similar cell) are also responsible for degrading calcified cartilage. Calcified cartilage is formed transiently in the growth plates of growing animals and is also present in the adult skeleton at the interfaces between bone and cartilage in all types of joints. In arthritis, accelerated resorption and bony remodeling will result in extensive resorption of calcified cartilage by osteoclasts. This process can release into the bloodstream collagen type II C-telopeptides (EKGPDPLQ (SEQ ID NO:10)) that are not recognized by 2B4.

Since the urinary form of the type II collagen telopeptide analyte is EKGPDP (SEQ ID NO:2) or smaller, proteases in the kidney and/or liver remove the C-terminal -LQ before release into the urine. Therefore, two sources of immunoreactive col2CTx are can be defined: (1) direct generation by chondrocytes activated to degrade their matrix collagen by MMPs, and (2) secondary generation in the kidney and/or liver from the circulating products of osteoclastic resorption of calcified cartilage.

In arthritis (rheumatoid arthritis (RA) and osteoarthritis (OA)) MMPs are known to be key agents in the destruction of the collagenous matrices of joint cartilages. In both forms of arthritis, bone structure is also greatly affected. In RA, osteoporosis is a common consequence both directly from the disease process itself through the effects of inflammatory cytokines and as a side effect of corticosteroid therapy. The accelerated bone resorption will be most pronounced in involved joints and will include removal of the calcified cartilage underlying joint surfaces. In OA, osteophytes (bony outgrowths) often feature prominently in the joint pathology. Here, too, calcified cartilage will be formed and then degraded (the latter by osteoclasts) as part of osteophyte growth. Therefore to monitor and manage both major forms of arthritis it would be desirable to differentially measure MMP-mediated and osteoclast-mediated (cathepsin K) collagen type II destruction. In blood or synovial fluid, measuring col2CTx (EKGPDP (SEQ ID NO:2)) can index the former activity, whereas measuring the osteoclast product (EKGPDPLQ (SEQ ID NO:10) in blood can index the latter. In addition, urinary col2CTx can provide an index of total resorption (both non-mineralized and mineralized cartilage). Such urine assays preferably include the steps of determining the creatinine content of the urine sample and correlating the ratio of the detected binding of the antibody to the creatinine content in order to provide a urinary index of total type II collagen resorption independent of urine volume.

The subject differential measurements of EKGPDP (SEQ ID NO:2), and EKGPDPLQ (SEQ ID NO:10) immunoreactivities have diagnostic value in the assessment of disease activity in the individual patient. In combination with measurement of a type I collagen marker to assess total bone resorption activity, and/or measurement of a type III collagen marker to assess other sources of non-mineralized connective tissue breakdown, an appropriate therapy can be prescribed and its desired effect monitored. Similarly, such differential assays can be used to identify new drug candidates (in vitro and in animals) and to provide surrogate markers in clinical trials for demonstrating desired beneficial effects on target tissues and cellular processes.

Representative assays for type I collagen resorption markers for this purpose include amino-terminal telopeptides of type I collagen (Osteomark®, Ostex International, Seattle, Wash.), carboxy-terminal telopeptides of type I collagen (CrossLaps®, Osteometer Biotech, Herlev, Denmark), and free lysyl pyridinoline cross-links (Pyrilinks®-D, Metra Biosystems, Mountain View, Calif.).

Representative assays for type III collagen resorption markers include amino-terminal telopeptides of type III collagen and carboxy-terminal telopeptides of type III collagen. Such assays are disclosed in U.S. Pat. Nos. 5,532,169, 5,641,687, and U.S. Ser. No. 08/923,175. Type III collagen resorption markers can be used to assess vascular collagen degradation (atherosclerosis), lung tissue degradation (e.g., emphysema and other destructive lung diseases), muscle wastage, frailty syndromes of the elderly, liver disease, hyperthyroidism, secondary effects of diabetes on connective tissue, and other inflammatory and infectious conditions that accelerate total bone resorption activity.

The invention also provides antibodies directed against other cross-linked carboxy-telopeptide degradation products of type II collagen, as well as linear peptides (SEQ ID NOS 11-20) synthesized to match the telopeptide components of the degradation products, and assays for cartilage degradation using the antibodies and linear peptides.

	SEQ	Body Fluid 1
	ID	Synovial
α1 (II) C Telopeptide Sequence	NO	fluid	Blood	Urine
EKGPD	1	—	N	N + M
EKGPDP	2	N	N	N + M
EKGPDPL	3	N	N	N + M
EKGPDPLQ	10	—	M	—
LGPREKGPDP	11	N	N	—
LGPREKGPDPLQ	12	N	N	—
LGPREKGPDPLQY	13	N	N	—
FAGLGPREKGPDP	14	N	N	—
FAGLGPREKGPDPLQ	15	N	N	—
FAGLGPREKGPDPLQY	16	N	N	—
IDMSAFAGLGPREKGPDP	17	N	N	—
IDMSAFAGLGPREKGPDPLQ	18	N	N	—
IDMSAFAGLGPREKGPDPLQY	19	N	N	—
EKGPDPLQYMR	20	N	N	—
1 Cartilage Source: N = non-mineralized cartilage;
M = mineralized cartilage;
N + M = total cartilage degradation; and
— = absent or only trace amounts.

The principal col2CTx degradation product is cross-linked EKGPDP. The further degradation product cross-linked EKGPD (SEQ ID NO:1) is usually present in urine in lower amounts. The cross-linked EKGPDPL (SEQ ID NO:3) degradation product is a minor component relative to cross-linked EKGPDP (SEQ ID NO:2).

Higher than normal levels of cross-linked EKGPDPLQ (SEQ ID NO:10) in blood can indicate mineralized cartilage degradation associated with active osteophyte formation in osteoarthritis.

The telopeptide sequences represented by SEQ ID NOS 11-13 result from metalloproteinase (MMP) cleavage of the G-L bond at the amino end of the α1(II)C telopeptide (SEQ ID NO 5), in combination with MMP cuts of the P-L, Q-Y, or Y-M bonds at the carboxy end of the telopeptide. SEQ ID NOS 14-16 represent related telopeptides from MMP cleavage between the A-F bond. SEQ ID NOS 17-19 represent longer telopeptides from MMP cleavage between the G-I bond. The amino ends of these longer telopeptides are generally metabolized further in the lymph nodes, liver, and/or kidney.

The telopeptide sequence represented by SEQ ID NO 20 results from serine protease cleavage of the R-E bond amino terminal to the cross-linking K residue, in combination with serine protease cleavage of the R-A bond at the carboxy end of the telopeptide.

Such cross-linking degradation products of SEQ ID NOS 11-19 (wherein the two telopeptide components are independently selected from among SEQ ID NOS 11-19), and SEQ ID NO 20, generally result from degradation of non-mineralized cartilage and are primarily found in synovial fluid and blood, and to a lesser extent in urine. Higher than normal levels of these degradation products in body fluids indicate active cartilage degradation that may correlate with rheumatoid arthritis, osteoarthritis, and other arthritides.

The invention also provides antibodies directed against cross-linked amino-telopeptide degradation products of type II collagen, as well as linear peptides (SEQ ID NOS 21-31) synthesized to match the telopeptide components of the degradation products, and assays for cartilage degradation using the antibodies and linear peptides.

	Body Fluid 2
	SEQ ID	Synovial
α1 (II) N Telopeptide Sequence 1	NO	fluid	Blood	Urine
DEKAGGA	21	N	N	N + M
DEKAGGAQ	22	N	N	N + M
DEKAGGAQL	23	N	N	N + M
FDEKAGGA	24	N	N	N + M
FDEKAGGAQ	25	N	N	N + M
FDEKAGGAQL	26	N	N	N + M
GGFDEKAGGAQLG	27	—	M	—
JMAGGFDEKAGGAQLG	28	—	M	—
JMAGGFDEKAGGAQLGV	29	N	N	—
FDEKAGGAQLGV	30	N	N	—
DEKAGGAQLGV	31	N	N	—
1 J = pyroglutamic acid, i.e., wholly cyclized pyrrolidone carboxylic acid (5-oxo-2-pyrrolidinecarboxylic acid).
2 Cartilage Source: N = non-mineralized cartilage;
M = mineralized cartilage;
N + M = total cartilage degradation; and
— = absent or only trace amounts.

The telopeptide sequences represented by SEQ ID NOS 21-23 result from metalloproteinase (MMP) cleavage of the F-D bond at the amino end of the α1(II)N telopeptide, in combination with MMP cuts of the A-Q, Q-L, or L-G bonds at the carboxy end of the telopeptide. SEQ ID NOS 24-26 represent related telopeptides from MMP cleavage between the G-F bond at the amino end. The amino and carboxy ends of the longer telopeptides (SEQ ID NOS 22-26) are generally metabolized further in the lymph nodes, liver, and/or kidney. As a result, the principal col2NTx degradation products in urine are cross-linked DEKAGGA and FDEKAGGA.

The telopeptide sequences represented by SEQ ID NOS 27-28 result from cathepsin K cleavage of the G-V bond at the carboxy end of the telopeptide, in combination with cathepsin K cleavage of the A-G bond at the amino end of the telopeptide in the case of SEQ ID NO 27. In the case of SEQ ID NO 28 the amino terminal J residue is blocked. Higher than normal levels of cross-linked GGFDEKAGGAQLG and QMAGGFDEKAGGAQLG in blood can indicate mineralized cartilage degradation associated with active osteophyte formation in osteoarthritis. Proteases in the kidney and/or liver remove the carboxy-terminal G residue before release into the urine.

The telopeptides represented by SEQ ID NOS 29-31 result from metalloproteinase cleavage of the V-M bond at the carboxy end of the telopeptide, in combination with MMP cleavage of the G-F or F-D bond at the amino end of the telopeptide in the case of SEQ ID NOS 30-31. Larger degradation products comprising SEQ ID NOS 29-31 plus some additional helical sequence(s) may also be present in synovial fluid and blood. These cross-linked telopeptides are generally metabolized further in the lymph nodes, liver, and/or kidney, and consequently occur only in trace amounts in urine.

As indicated above, cross-linked α1(II)N telopeptides represented by SEQ ID NOS 27-31 are produced at the site(s) of cartilage degradation but degraded further during passage through the lymph nodes, liver, and/or kidney. The resulting smaller degradation products have two telopeptide components that may be independently selected from among SEQ ID NOS 21-26. Higher than normal levels of these degradation products in urine indicate total cartilage degradation that may correlate with rheumatoid arthritis, osteoarthritis, and other arthritides.

Thus the invention provides, in a first embodiment, an improved method of analyzing a body fluid sample for the presence of an analyte indicative of a physiological condition, including the steps of contacting the body fluid sample with an antibody which binds to the analyte, detecting binding of the antibody in the body fluid sample, and correlating any detected binding to the physiological condition, the improvement comprising contacting a serum sample with an antibody which binds to

wherein K-K-K is hydroxylysyl pyridinoline or lysyl pyridinoline, and correlating any detected binding to resorption of non-mineralized type II collagen in vivo.

In a second embodiment, the invention provides an improved method of analyzing a body fluid sample for the presence of an analyte indicative of a physiological condition, including the steps of contacting the body fluid sample with an antibody which binds to the analyte, detecting binding of the antibody in the body fluid sample, and correlating any detected binding to the physiological condition, the improvement comprising contacting a serum sample with an antibody which binds to

wherein K-K-K is hydroxylysyl pyridinoline or lysyl pyridinoline, and correlating any detected binding to resorption of mineralized type II collagen in vivo.

In a third embodiment, the invention provides an improved method of analyzing a body fluid sample for the presence of an analyte indicative of a physiological condition, including the steps of contacting the body fluid sample with an antibody which binds to the analyte, detecting binding of the antibody in the body fluid sample, and correlating any detected binding to the physiological condition, the improvement comprising contacting a urine sample with an antibody which binds to

wherein K-K-K is hydroxylysyl pyridinoline or lysyl pyridinoline, and correlating any detected binding to resorption of both non-mineralized and mineralized type II collagen in vivo.

In a fourth embodiment, the invention provides an improved method of analyzing a body fluid sample for the presence of an analyte indicative of a physiological condition, including the steps of contacting the body fluid sample with an antibody which binds to the analyte, detecting binding of the antibody in the body fluid sample, and correlating any detected binding to the physiological condition, the improvement comprising contacting a serum sample with a first antibody which binds to

and contacting the serum sample with a second antibody which binds to

wherein K-K-K is hydroxylysyl pyridinoline or lysyl pyridinoline, and correlating the total detected binding of the first and second antibodies to resorption of both mineralized and non-mineralized type II collagen in vivo.

In a fifth embodiment, the invention provides an improved method of analyzing a body fluid sample for the presence of an analyte indicative of a physiological condition, including the steps of contacting the body fluid sample with an antibody which binds to the analyte, detecting binding of the antibody in the body fluid sample, and correlating any detected binding to the physiological condition, the improvement comprising contacting a serum sample with a first antibody which binds to

and contacting a urine sample with a second antibody which binds to

wherein K-K-K is hydroxylysyl pyridinoline or lysyl pyridinoline, and correlating any detected binding of the first antibody to resorption of mineralized type II collagen in vivo, and any detected binding of the second antibody to resorption of both mineralized and non-mineralized type II collagen in vivo.

The term “antibody” in this disclosure is meant to encompass polyclonal antibodies, monoclonal antibodies, and antigen-binding fragments thereof. Such EKGPDPLQ-binding and EKGPDP-binding antibodies, or GGFDEKAGGAQLG-binding and DEKAGGA-binding antibodies, can be produced by standard methods well known in the art. A representative protocol follows.

EKGPDPLQ hybridoma development: Female RFB/DnJ mice are injected intraperitoneal (ip) with an emulsion of complete Freund's adjuvant and EKGPDPLQ synthetic peptide cross-linked to the carrier protein keyhole limpet hemacyanin (KLH) via glutaraldehyde (KLH-EKGPDPLQ). One month later a booster injection of KLH-EKGPDPLQ is given ip in an emulsion with incomplete Freund's adjuvant. Approximately eight weeks later the mice are sacrificed and splenocytes fused, by polyethylene glycol, to the FOX-NY murine myeloma cell line (ATCC CRL-1732). Fusion cells are grown in 96-well plates in selection media containing adenine, aminopterin and thymidine (AAT).

Approximately one week after fusion hybridoma colony culture supernatants are tested in ELISA for reactivity to the EKGPDPLQ synthetic peptide cross-linked via glutaraldehyde to bovine serum albumin (BSA-EKGPDPLQ). Hybridoma colonies producing antibody reactive with BSA-EKGPDPLQ are secondarily tested for specificity of reaction in ELISA against other synthetic peptide sequences. Among those tested are EKGPDP synthetic peptide cross-linked to BSA via glutaraldehyde (BSA-EKGPDP). Hybridoma colonies that react positively to BSA-EKGPDPLQ and negatively to BSA-EKGPDP are cryopreserved. Representative hybridomas are cloned to monoclonality by the limited dilution method.

In competition ELISA, human serum specimens as well as soluble BSA-EKGPDPLQ are found to compete with solid phase BSA-EKGPDPLQ for candidate antibodies.

A cathepsin K digest of type II collagen can also be prepared for immunization and screening purposes. Proteoglycans are extracted from a tissue sample of human articular cartilage with a protein denaturant, such as 4 M guanidine HCl. The residue is washed with water and digested with recombinant cathepsin K (37° C., pH 5.8). The digest is fractionated by high performance liquid chromatography, for example by reverse phase, and fractions containing pyridinoline cross-links are monitored by fluorescence emission at 390 nm (297 nm excitation). The fluorescent fraction containing the cross-linked C-telopeptides of sequence EKGPDPLQ (SEQ ID NO:10) is identified by N-terminal sequence analysis. This fraction can be used for screening purposes and for validation of antibody specificity.

The subject antibodies can be employed in a variety of immunoassay formats that are well known in the art. For example, see: Harlow & Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, pp. 553-612, 1988; Principles and Practice of Immunoassay, Price & Newman (Eds.), Stockton Press, 1991; and Immunoassay, Diamandis & Christopoulos (Eds.), Academic Press, 1996.

While the invention has been described in conjunction with preferred embodiments, one of ordinary skill after reading the foregoing specification will be able to effect various changes, substitutions of equivalents, and alterations to the subject matter set forth herein. Hence, the invention can be practiced in ways other than those specifically described herein.

31 1 5 PRT Homo sapiens PEPTIDE (1)..(5) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 1Glu Lys Gly Pro Asp1 5 2 6 PRT Homo sapiens PEPTIDE (1)..(5) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 2Glu Lys Gly Pro Asp Pro1 5 3 7 PRT Homo sapiens PEPTIDE (1)..(7) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 3Glu Lys Gly Pro Asp Pro Leu1 5 4 14 PRT Homo sapiens PEPTIDE (1)..(14) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 4Ala Phe Ala Gly Leu Gly Pro Arg Glu Lys Gly Pro Asp Pro1 5 10 5 20 PRT Homo sapiens PEPTIDE (1)..(20) ssyn- corr. to C-terminal telopeptide seq. of hu. type II collagen 5Ala Phe Ala Gly Leu Gly Pro Arg Glu Lys Gly Pro Asp Pro Leu Gln1 5 10 15Tyr Met Arg Ala 20 6 16 PRT Homo sapiens PEPTIDE (1)..(16) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 6Ala Phe Ala Gly Leu Gly Pro Arg Glu Lys Gly Pro Asp Pro Leu Gln1 5 10 15 7 17 PRT Homo sapiens PEPTIDE (1)..(17) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 7Ala Phe Ala Gly Leu Gly Pro Arg Glu Lys Gly Pro Asp Pro Leu Gln1 5 10 15Tyr 8 6 PRT Homo sapiens PEPTIDE (1)..(6) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 8Leu Gln Tyr Met Arg Ala1 5 9 4 PRT Homo sapiens PEPTIDE (1)..(4) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 9Tyr Met Arg Ala1 10 8 PRT Homo sapiens PEPTIDE (1)..(8) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 10Glu Lys Gly Pro Asp Pro Leu Gln1 5 11 10 PRT Homo sapiens PEPTIDE (1)..(10) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 11Leu Gly Pro Arg Glu Lys Gly Pro Asp Pro1 5 10 12 12 PRT Homo sapiens PEPTIDE (1)..(12) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 12Leu Gly Pro Arg Glu Lys Gly Pro Asp Pro Leu Gln1 5 10 13 13 PRT Homo sapiens PEPTIDE (1)..(13) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 13Leu Gly Pro Arg Glu Lys Gly Pro Asp Pro Leu Gln Tyr1 5 10 14 13 PRT Homo sapiens PEPTIDE (1)..(13) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 14Phe Ala Gly Leu Gly Pro Arg Glu Lys Gly Pro Asp Pro1 5 10 15 15 PRT Homo sapiens PEPTIDE (1)..(15) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 15Phe Ala Gly Leu Gly Pro Arg Glu Lys Gly Pro Asp Pro Leu Gln1 5 10 15 16 16 PRT Homo sapiens PEPTIDE (1)..(16) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 16Phe Ala Gly Leu Gly Pro Arg Glu Lys Gly Pro Asp Pro Leu Gln Tyr1 5 10 15 17 18 PRT Homo sapiens PEPTIDE (1)..(18) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 17Ile Asp Met Ser Ala Phe Ala Gly Leu Gly Pro Arg Glu Lys Gly Pro1 5 10 15Asp Pro 18 20 PRT Homo sapiens PEPTIDE (1)..(20) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 18Ile Asp Met Ser Ala Phe Ala Gly Leu Gly Pro Arg Glu Lys Gly Pro1 5 10 15Asp Pro Leu Gln 20 19 21 PRT Homo sapiens PEPTIDE (1)..(21) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 19Ile Asp Met Ser Ala Phe Ala Gly Leu Gly Pro Arg Glu Lys Gly Pro1 5 10 15Asp Pro Leu Gln Tyr 20 20 11 PRT Homo sapiens PEPTIDE (1)..(11) syn- corr. to C-terminal telopeptide seq. of hu. type II collagen 20Glu Lys Gly Pro Asp Pro Leu Gln Tyr Met Arg1 5 10 21 7 PRT Homo sapiens PEPTIDE (1)..(7) syn- corr. to N-terminal telopeptide seq. of hu. type II collagen 21Asp Glu Lys Ala Gly Gly Ala1 5 22 8 PRT Homo sapiens PEPTIDE (1)..(8) syn- corr. to N-terminal telopeptide seq. of hu. type II collagen 22Asp Glu Lys Ala Gly Gly Ala Gln1 5 23 9 PRT Homo sapiens PEPTIDE (1)..(9) syn- corr. to N-terminal telopeptide seq. of hu. type II collagen 23Asp Glu Lys Ala Gly Gly Ala Gln Leu1 5 24 8 PRT Homo sapiens PEPTIDE (1)..(8) syn- corr. to N-terminal telopeptide seq. of hu. type II collagen 24Phe Asp Glu Lys Ala Gly Gly Ala1 5 25 9 PRT Homo sapiens PEPTIDE (1)..(9) syn- corr. to N-terminal telopeptide seq. of hu. type II collagen 25Phe Asp Glu Lys Ala Gly Gly Ala Gln1 5 26 10 PRT Homo sapiens PEPTIDE (1)..(10) syn- corr. to N-terminal telopeptide seq. of hu. type II collagen 26Phe Asp Glu Lys Ala Gly Gly Ala Gln Leu1 5 10 27 13 PRT Homo sapiens PEPTIDE (1)..(13) syn- corr. to N-terminal telopeptide seq. of hu. type II collagen 27Gly Gly Phe Asp Glu Lys Ala Gly Gly Ala Gln Leu Gly1 5 10 28 16 PRT Homo sapiens PEPTIDE (1)..(16) syn- corr. to N-terminal telopeptide seq. of hu. type II collagen 28Xaa Met Ala Gly Gly Phe Asp Glu Lys Ala Gly Gly Ala Gln Leu Gly1 5 10 15 29 17 PRT Homo sapiens PEPTIDE (1)..(17) syn- corr. to N-terminal telopeptide seq. of hu. type II collagen 29Xaa Met Ala Gly Gly Phe Asp Glu Lys Ala Gly Gly Ala Gln Leu Gly1 5 10 15Val 30 12 PRT Homo sapiens PEPTIDE (1)..(12) syn- corr. to N-terminal telopeptide seq. of hu. type II collagen 30Phe Asp Glu Lys Ala Gly Gly Ala Gln Leu Gly Val1 5 10 31 11 PRT Homo sapiens PEPTIDE (1)..(11) syn- corr. to N-terminal telopeptide seq. of hu. type II collagen 31Asp Glu Lys Ala Gly Gly Ala Gln Leu Gly Val1 5 10

Claims

1. A synthetic peptide selected from among LGPREKGPDP (SEQ ID NO:11), LGPREKGPDPLQ (SEQ ID NO:12), and LGPREKGPDPLQY (SEQ ID NO:13).

2. A synthetic peptide selected from among FAGLGPREKGPDP (SEQ ID NO:14), FAGLGPREKGPDPLQ (SEQ ID NO:15), and FAGLGPREKGPDPLQY (SEQ ID NO:16).

3. A synthetic peptide selected from among IDMSAFAGLGPREKGPDP (SEQ ID NO:17), IDMSAFAGLGPREKGPDPLQ (SEQ ID NO:18), and IDMSAFAGLGPREKGPDPLQY (SEQ ID NO 19).

4. Synthetic peptide EKGPDPLQYMR (SEQ ID NO 20).