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J Biol Chem, Vol. 274, Issue 10, 6183-6189, March 5, 1999
2,8-Linked Oligo/Polysialic
Acids Studied by High Performance Anion-exchange Chromatography
From the Biology Department, The Johns Hopkins University,
Baltimore, Maryland 21218
Recent studies from many laboratories revealed
remarkable structural, distributional, and functional diversities of
oligo/polysialic acids (OSA/PSA) that exist in organisms ranging from
bacteria to man. These diversities are further complicated by the fact that OSA/PSA spontaneously form lactones under even mildly acidic conditions. By using high performance anion-exchange chromatography (HPAEC) with nitrate eluents, we found that lactonization of
2,8-linked OSA/PSA (oligo/poly-Neu5Ac, oligo/poly-Neu5Gc and
oligo/poly-KDN) proceeds readily, and the lactonization process
displays three discrete stages. The initial stage is characterized by
limited lactonization occurring between two internal sialic acid
residues, reflected by a regular pattern of lactone peaks
interdigitated with non-lactonized peaks on HPAEC. In the middle stage,
multiple lactonized species are formed from a molecule with a given
degree of polymerization (DP), in which the maximum number of lactone rings formed equals DP minus 2. At the final stage, completely lactonized species become the major components, resulting in drastic changes in the physicochemical properties of the sample.
Interestingly, the smallest lactonizable OSA are tetramer, trimer, and
dimer at the initial, middle, and final stages, respectively. At any of
the stages, OSA/PSA of higher DP lactonize more rapidly, but all the
lactone rings rapidly open up when exposed to mild alkali. Lactonized
OSA/PSA are resistant to both enzyme- and acid-catalyzed glycosidic
bond cleavage. The latter fact was utilized to obtain more high DP
oligo/poly(
2,8-Neu5Gc) chains from a polysialoglycoprotein. Our
results should be useful in preparation, storage, and analysis of
OSA/PSA. Possible biological significance and bioengineering potentials
of lactonization are discussed.
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