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. 1998 Oct;7(10):2175–2183. doi: 10.1002/pro.5560071015

Topological mimicry and epitope duplication in the guanylyl cyclase C receptor.

A Nandi 1, K Suguna 1, A Surolia 1, S S Visweswariah 1
PMCID: PMC2143839  PMID: 9792105

Abstract

Guanylyl cyclase C (GCC) is the receptor for the gastrointestinal hormones, guanylin, and uroguanylin, in addition to the bacterial heat-stable enterotoxins, which are one of the major causes of watery diarrhea the world over. GCC is expressed in intestinal cells, colorectal tumor tissue and tumors originating from metastasis of the colorectal carcinoma. We have earlier generated a monoclonal antibody to human GCC, GCC:B10, which was useful for the immunohistochemical localization of the receptor in the rat intestine (Nandi A et al., 1997, J Cell Biochem 66:500-511), and identified its epitope to a 63-amino acid stretch in the intracellular domain of GCC. In view of the potential that this antibody has for the identification of colorectal tumors, we have characterized the epitope for GCC:B10 in this study. Overlapping peptide synthesis indicated that the epitope was contained in the sequence HIPPENIFPLE. This sequence was unique to GCC, and despite a short stretch of homology with serum amyloid protein and pertussis toxin, no cross reactivity was detected. The core epitope was delineated using a random hexameric phage display library, and two categories of sequences were identified, containing either a single, or two adjacent proline residues. No sequence identified by phage display was identical to the epitope present in GCC, indicating that phage sequences represented mimotopes of the native epitope. Alignment of these sequences with HIPPENIFPLE suggested duplication of the recognition motif, which was confirmed by peptide synthesis. These studies allowed us not only to define the requirements of epitope recognition by GCC:B10 monoclonal antibody, but also to describe a novel means of epitope recognition involving topological mimicry and probable duplication of the cognate epitope in the native guanylyl cyclase C receptor sequence.

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Selected References

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  1. Bhardwaj D., Singh S. S., Abrol S., Chaudhary V. K. Monoclonal antibodies against a minor and the major coat proteins of filamentous phage M13: their application in phage display. J Immunol Methods. 1995 Feb 27;179(2):165–175. doi: 10.1016/0022-1759(94)00280-a. [DOI] [PubMed] [Google Scholar]
  2. Carrithers S. L., Barber M. T., Biswas S., Parkinson S. J., Park P. K., Goldstein S. D., Waldman S. A. Guanylyl cyclase C is a selective marker for metastatic colorectal tumors in human extraintestinal tissues. Proc Natl Acad Sci U S A. 1996 Dec 10;93(25):14827–14832. doi: 10.1073/pnas.93.25.14827. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Carrithers S. L., Parkinson S. J., Goldstein S. D., Park P. K., Urbanski R. W., Waldman S. A. Escherichia coli heat-stable enterotoxin receptors. A novel marker for colorectal tumors. Dis Colon Rectum. 1996 Feb;39(2):171–181. doi: 10.1007/BF02068072. [DOI] [PubMed] [Google Scholar]
  4. Carrithers S. L., Parkinson S. J., Goldstein S., Park P., Robertson D. C., Waldman S. A. Escherichia coli heat-stable toxin receptors in human colonic tumors. Gastroenterology. 1994 Dec;107(6):1653–1661. doi: 10.1016/0016-5085(94)90804-4. [DOI] [PubMed] [Google Scholar]
  5. Cha S., Leung P. S., Van de Water J., Tsuneyama K., Joplin R. E., Ansari A. A., Nakanuma Y., Schatz P. J., Cwirla S., Fabris L. E. Random phage mimotopes recognized by monoclonal antibodies against the pyruvate dehydrogenase complex-E2 (PDC-E2). Proc Natl Acad Sci U S A. 1996 Oct 1;93(20):10949–10954. doi: 10.1073/pnas.93.20.10949. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chao A. C., de Sauvage F. J., Dong Y. J., Wagner J. A., Goeddel D. V., Gardner P. Activation of intestinal CFTR Cl- channel by heat-stable enterotoxin and guanylin via cAMP-dependent protein kinase. EMBO J. 1994 Mar 1;13(5):1065–1072. doi: 10.1002/j.1460-2075.1994.tb06355.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cohen S. A., Strydom D. J. Amino acid analysis utilizing phenylisothiocyanate derivatives. Anal Biochem. 1988 Oct;174(1):1–16. doi: 10.1016/0003-2697(88)90512-x. [DOI] [PubMed] [Google Scholar]
  8. Currie M. G., Fok K. F., Kato J., Moore R. J., Hamra F. K., Duffin K. L., Smith C. E. Guanylin: an endogenous activator of intestinal guanylate cyclase. Proc Natl Acad Sci U S A. 1992 Feb 1;89(3):947–951. doi: 10.1073/pnas.89.3.947. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Demangel C., Lafaye P., Mazie J. C. Reproducing the immune response against the Plasmodium vivax merozoite surface protein 1 with mimotopes selected from a phage-displayed peptide library. Mol Immunol. 1996 Aug;33(11-12):909–916. doi: 10.1016/s0161-5890(96)00058-2. [DOI] [PubMed] [Google Scholar]
  10. Drewett J. G., Garbers D. L. The family of guanylyl cyclase receptors and their ligands. Endocr Rev. 1994 Apr;15(2):135–162. doi: 10.1210/edrv-15-2-135. [DOI] [PubMed] [Google Scholar]
  11. Emsley J., White H. E., O'Hara B. P., Oliva G., Srinivasan N., Tickle I. J., Blundell T. L., Pepys M. B., Wood S. P. Structure of pentameric human serum amyloid P component. Nature. 1994 Jan 27;367(6461):338–345. doi: 10.1038/367338a0. [DOI] [PubMed] [Google Scholar]
  12. Feller S. M., Ren R., Hanafusa H., Baltimore D. SH2 and SH3 domains as molecular adhesives: the interactions of Crk and Abl. Trends Biochem Sci. 1994 Nov;19(11):453–458. doi: 10.1016/0968-0004(94)90129-5. [DOI] [PubMed] [Google Scholar]
  13. Fontenot J. D., Mariappan S. V., Catasti P., Domenech N., Finn O. J., Gupta G. Structure of a tumor associated antigen containing a tandemly repeated immunodominant epitope. J Biomol Struct Dyn. 1995 Oct;13(2):245–260. doi: 10.1080/07391102.1995.10508837. [DOI] [PubMed] [Google Scholar]
  14. Garbers D. L. Guanylyl cyclase receptors and their endocrine, paracrine, and autocrine ligands. Cell. 1992 Oct 2;71(1):1–4. doi: 10.1016/0092-8674(92)90258-e. [DOI] [PubMed] [Google Scholar]
  15. Geysen H. M., Mason T. J., Rodda S. J. Cognitive features of continuous antigenic determinants. J Mol Recognit. 1988 Feb;1(1):32–41. doi: 10.1002/jmr.300010107. [DOI] [PubMed] [Google Scholar]
  16. Geysen H. M., Meloen R. H., Barteling S. J. Use of peptide synthesis to probe viral antigens for epitopes to a resolution of a single amino acid. Proc Natl Acad Sci U S A. 1984 Jul;81(13):3998–4002. doi: 10.1073/pnas.81.13.3998. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Geysen H. M., Rodda S. J., Mason T. J., Tribbick G., Schoofs P. G. Strategies for epitope analysis using peptide synthesis. J Immunol Methods. 1987 Sep 24;102(2):259–274. doi: 10.1016/0022-1759(87)90085-8. [DOI] [PubMed] [Google Scholar]
  18. Nandi A., Bhandari R., Visweswariah S. S. Epitope conservation and immunohistochemical localization of the guanylin/stable toxin peptide receptor, guanylyl cyclase C. J Cell Biochem. 1997 Sep 15;66(4):500–511. doi: 10.1002/(sici)1097-4644(19970915)66:4<500::aid-jcb9>3.0.co;2-p. [DOI] [PubMed] [Google Scholar]
  19. Oldenburg K. R., Loganathan D., Goldstein I. J., Schultz P. G., Gallop M. A. Peptide ligands for a sugar-binding protein isolated from a random peptide library. Proc Natl Acad Sci U S A. 1992 Jun 15;89(12):5393–5397. doi: 10.1073/pnas.89.12.5393. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Pacholczyk T., Sweadner K. J. Epitope and mimotope for an antibody to the Na, K-ATPase. Protein Sci. 1997 Jul;6(7):1537–1548. doi: 10.1002/pro.5560060718. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Scott J. K., Loganathan D., Easley R. B., Gong X., Goldstein I. J. A family of concanavalin A-binding peptides from a hexapeptide epitope library. Proc Natl Acad Sci U S A. 1992 Jun 15;89(12):5398–5402. doi: 10.1073/pnas.89.12.5398. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Scott J. K., Smith G. P. Searching for peptide ligands with an epitope library. Science. 1990 Jul 27;249(4967):386–390. doi: 10.1126/science.1696028. [DOI] [PubMed] [Google Scholar]
  23. Smith G. P., Scott J. K. Libraries of peptides and proteins displayed on filamentous phage. Methods Enzymol. 1993;217:228–257. doi: 10.1016/0076-6879(93)17065-d. [DOI] [PubMed] [Google Scholar]
  24. Smith T. J., Chase E. S., Schmidt T. J., Olson N. H., Baker T. S. Neutralizing antibody to human rhinovirus 14 penetrates the receptor-binding canyon. Nature. 1996 Sep 26;383(6598):350–354. doi: 10.1038/383350a0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Stein P. E., Boodhoo A., Armstrong G. D., Cockle S. A., Klein M. H., Read R. J. The crystal structure of pertussis toxin. Structure. 1994 Jan 15;2(1):45–57. doi: 10.1016/s0969-2126(00)00007-1. [DOI] [PubMed] [Google Scholar]
  26. Stoute J. A., Ballou W. R., Kolodny N., Deal C. D., Wirtz R. A., Lindler L. E. Induction of humoral immune response against Plasmodium falciparum sporozoites by immunization with a synthetic peptide mimotope whose sequence was derived from screening a filamentous phage epitope library. Infect Immun. 1995 Mar;63(3):934–939. doi: 10.1128/iai.63.3.934-939.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Yu H., Chen J. K., Feng S., Dalgarno D. C., Brauer A. W., Schreiber S. L. Structural basis for the binding of proline-rich peptides to SH3 domains. Cell. 1994 Mar 11;76(5):933–945. doi: 10.1016/0092-8674(94)90367-0. [DOI] [PubMed] [Google Scholar]
  28. de Sauvage F. J., Camerato T. R., Goeddel D. V. Primary structure and functional expression of the human receptor for Escherichia coli heat-stable enterotoxin. J Biol Chem. 1991 Sep 25;266(27):17912–17918. [PubMed] [Google Scholar]

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