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J Biol Chem, Vol. 274, Issue 51, 36550-36558, December 17, 1999

Structural and Immunochemical Characterization of a Neisseria gonorrhoeae Epitope Defined by a Monoclonal Antibody 2C7; the Antibody Recognizes a Conserved Epitope on Specific Lipo-oligosaccharides in Spite of the Presence of Human Carbohydrate Epitopes*

Ryohei YamasakiDagger §, Hiroyuki Koshino, Sadamu Kurono, Yumiko NishinakaDagger , Daniel P. McQuillen||, Akiko KumeDagger , Sunita Gulati||, and Peter A. Rice||

From the Dagger  Department of Biochemistry and Biotechnology, Tottori University, Tottori 680-8553, the  Institute of Physical and Chemical Research (Riken), Wako 351-0198, Japan, and the || Maxwell Finland Laboratory for Infectious Diseases, Evans Memorial Department of Clinical Research and Department of Medicine, Boston University, Boston, Massachusetts 02118

Lipo-oligosaccharides (LOS) produced by Neisseria gonorrhoeae are important antigenic and immunogenic components of the outer membrane complex. Previously, we showed that murine monoclonal antibody (mAb) 2C7 did not cross-react with human glycosphingolipids but identified the LOS epitope that is widely expressed in vivo and in vitro (Gulati, S., McQuillen, D. P., Mandrell, R. E., Jani, D. B., and Rice, P. A. (1996) J. Infect. Dis. 174, 1223-1237). In the present study, we analyzed the structure of gonococcal strain WG LOS containing the 2C7 epitope and investigated the structural requirements for expression of the epitope. We determined that the WG LOS components are Hep[1]-elongated forms of 15253 LOS that have a lactose on both Hep[1] and Hep[2] (Yamasaki, R., Kerwood, D. E., Schneider, H., Quinn, K. P., Griffiss, J. M., and Mandrell, R. E. (1994) J. Biol. Chem. 269, 30345-30351). In addition, we found that expression of the 2C7 epitope within the LOS is blocked when the Hep[2]-lactose is elongated. Based on the structural data of these LOS and the results obtained from immunochemical analyses, we conclude the following: 1) mAb 2C7 requires both the 15253 OS minimum structure and the N-linked fatty acids in the lipoidal moiety for expression of the epitope; 2) mAb 2C7 binds to the LOS that elongates the lactose on Hep[1] of the 15253 OS, but not the one on Hep[2]; and 3) the 2C7 epitope is expressed on gonococcal LOS despite the presence of human carbohydrate epitopes such as a lactosamine or its N-acetylgalactosaminylated (globo) form. Our study shows that the conserved epitope defined by mAb 2C7 could potentially be used as a safe site for the development of a vaccine candidate.


* This work was supported in part by National Institutes of Health Grants AI01061 and AI32725 and Grant-in-aid for Scientific Research of the Ministry of Education of Japan 10306022.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

§ To whom correspondence should be addressed: Dept. of Biochemistry & Biotechnology, Tottori University, Koyama-Minami-4-101, Tottori City, Tottori-Ken 680-8553, Japan. Tel.: 81-857-31-6751, Fax: 81-857-31-5347; E-mail: yamasaki@muses.tottori-u.ac.jp.


Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.



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