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Originally published In Press as doi:10.1074/jbc.M508762200 on September 19, 2005
J. Biol. Chem., Vol. 280, Issue 46, 38305-38316, November 18, 2005
Degree of Polymerization (DP) of Polysialic Acid (PolySia) on Neural Cell Adhesion Molecules (N-CAMs)
DEVELOPMENT AND APPLICATION OF A NEW STRATEGY TO ACCURATELY DETERMINE THE DP OF polySIA CHAINS ON N-CAMS*
Daisuke Nakata and
Frederic A. Troy, II1
From the
Department of Biochemistry and Molecular Medicine, University of California School of Medicine, Davis, California 95616
2,8-Linked polysialic acid (polySia) is a structurally unique antiadhesive glycotope that covalently modifies N-linked glycans on neural cell adhesion molecules (N-CAMs). These sugar chains play a key role in modulating cell-cell interactions, principally during embryonic development, neural plasticity, and tumor metastasis. The degree of polymerization (DP) of polySia chains on N-CAM is postulated to be of critical importance in regulating N-CAM function. There are limitations, however, in the conventional methods to accurately determine the DP of polySia on N-CAM, the most serious being partial acid hydrolysis of internal 2,8-ketosidic linkages that occur during fluorescent derivatization, a step necessary to enhance chromatographic detection. To circumvent this problem, we have developed a facile method that combines the use of Endo- -galactosidase to first release linear polySia chains from N-CAM, with high resolution high pressure liquid chromatography profiling. This strategy avoids acid hydrolysis prior to chromatographic profiling and thus provides an accurate determination of the DP and distribution of polySia on N-CAM. The potential of this new method was evaluated using a nonpolysialylated construct of N-CAM that was polysialylated in vitro using a soluble construct of ST8Sia II or ST8Sia IV. Whereas most of the oligosialic acid/polySia chains consisted of DPs 5060 or less, a subpopulation of chains with DPs 150 to 180 and extending to DP 400 were detected. The DP of this subpopulation is considerably greater than reported previously for N-CAM. Endo- -galactosidase can also release polySia chains from polysialylated membranes expressed in the neuroblastoma cell line, Neuro2A, and native N-CAM from embryonic chick brains.
Received for publication, August 9, 2005
, and in revised form, September 8, 2005.
* This work was supported in part by National Institutes of Health Grant GM55703 and University of California Tobacco-related Disease Research Program Grant 12RT-0254. A preliminary report of this work has appeared in abstract form (1). The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
1 To whom correspondence should be addressed: Dept. of Biochemistry and MolecularMedicine, University of California School of Medicine, Tupper Hall, Davis, CA 95616. Tel.: 530-752-3240; Fax: 530-752-3516; E-mail: fatroy{at}ucdavis.edu.

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Copyright © 2005 by the American Society for Biochemistry and Molecular Biology.
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