Ribosomal P Antigen

The Ribosomal P antigen consists of three proteins of the 60S ribosomal subunit (3). These three proteins are designated PO(38 kD), P1(19 kD), and P2(17 kD). Studies have suggested that one P1 homodimer and one P2 homodimer are attached to PO by the NH2-termini (4). P1 and P2 are believed to be the eukaryotic equivalent of the E. coli ribosomal protein L12 and have been shown to contain sequences that are highly conserved among eukaryotes (5). The major immunoreactive epitope of these ribosomal antigens has been mapped and is localized to the carboxy terminus. PO, P1, and P2 have an identical 17 amino acid carboxy terminus. The Ribosomal P antigens have GTPase activity (6) and have been shown to be phosphorylated by casein kinase II (7). \n\nAutoantibodies to Ribosomal antigens were originally described inpatients with Systemic Lupus Erythematosus (SLE), and have been associated with psychotic episodes in SLE (1). Anti-P antibodies are detected in the sera of 10-20% of SLE patients and are found in 80% of patients with Lupus Psychosis as opposed to SLE patients with other neurological manifestations (2). \n\nThe results of one study have indicated that Anti-P antibodies show moderate restriction in spectrotype, isotype, subclass, and light chain type. (8) It has also been shown that Anti-Ribosomal P antisera may contain antibodies to a small fragment of 28SrRNA (6). Another study has shown a high frequency of Anti-Ro/SS-A in patients with Anti-P, while Anti-La/SS-B is present only in a low frequency (1). Other studies have presented evidence that Anti-P antibodies (IgG) may bind to the ribosome in vivo and inhibit protein synthesis (9). The original method for determining antibodies to ribosomal proteins was immunofluorescence. \n\nRecent developments in ELISA methodology have increased the sensitivity and the ability of the diagnostician to quantitate patient antibody titers.\n\nApplications: \nSuitable for use in ELISA. Other applications not tested.\n\nRecommended Dilution:\nELISA: Recommended for use in standard solid phase immunoassays.\nOptimal dilutions to be determined by the researcher.\n\nActivity:\nOne unit of activity is defined as the amount of antigen that will generate an absorbance of 1.2 when assayed using standard procedures for enzyme immunoassay. Activity will vary with assay conditions.\n\nStorage and Stability:\nR2031-27 is unstable above 0 degrees C. Aliquot and store at -70 degrees C. Aliquots are stable for at least 6 months at -70 degrees C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.\n

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SPECIFICATIONS

Catalog Number

R2031-27

Size

1000U

Applications

ELISA

Form

Supplied as a liquid in 0.01M Tris, 0.5M sodium chloride, 0.02% sodium azide.

Purity

Purified from bovine and/or rabbit thymus through the use of immobilized human anti-Ribosomal P immune globulins. Other antigens (Sm, RNP, Scl-70, SSA(Ro), SSB(La), Jo-1) are not detected with ELISA assays.

References

1. Bonfa E., Golombek SJ, Kaufman LD, Skelly S, et al. \"Association Between Lupus Psychosis and Anti-Ribosomal P Protein Antibodies.\" New England J of Med, 1987, pg 265-271. \n2. Elkon K, Weissbach H, Brot N. \"Central Nervous System Function in Systemic Lupus Erythematosus.\"Neurochemical Research, 1990, pg 401-406. \n3. Elkon KB, Pamassa AP, Foster C.L. J Exp Med, 1985, pg 459-471. \n4. Uchiumi T Wahba AJ, Traut RR. Proc Natl Acad Sci, 1987, pg 5580-5584. \n5. Towbin H, Ramjoue H-P, Kuster H, Liverani D, Gordon J. J Bio Chem, Vol 257: 1982, pg 12709-12715. \n6. Jia-Li Chu, Brot N, Weissbach H, Elkon K. \"Lupus Anti-ribosomal P Anitsera Contain Antibodies to a Small Fragment of 28S rRNA Located in the Proposed Ribosomal GTPase Center.\" J Exp Med, 1991, pg 507-514. \n7. Hasler P, Brot N, Weissbach H, et al. \"Ribosomal Proteins PO, P1, and P2 Are Phosphorylated by Casein Kinase II at Their Conserved Carboxyl Termini.\" J of Bio Chem, Vol: 266, 1991, pg 13815-13820. \n8. Bonfa E, Jia-Li-Chu, Brot N, and Elkon KB. \"Lupus Anti-Ribosomal P Peptide Antibodies Show Limited Heterogeneity and Are Predominantly of the IgG, and IgG2 Subclasses.\" Clinical Immunology and Immunopathology , Vol: 45, 1987, pg 129-138. \n9. Stacey DW, Skelly S, Watson T, Elkon K, et al. \"The Inhibition of Protein Synthesis by IgG Containing Anti-ribosome P Autoantibodies from Systemic Lupus Erythematosus Patients.\" Archives of Biochemistry and Biophysics, Vol: 267, 1988, pg 398-403. \n