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. 1999 Mar;67(3):1405–1414. doi: 10.1128/iai.67.3.1405-1414.1999

TABLE 3.

Molecular weight analysis of O-deacylated LOS by electrospray MS for MA-1 and MA-1 galE

N. meningitidis strain LOS Observed (calculated) mol wta Relative abundanceb by MALDI (ESI) Proposed compositionc
MA-1 LOS B 2,428.0 (2,428.22) 50 (36) Hex2-Hep2-GlcNAc-PEA1-Kdo2-lipid A
LOS B′ 2,551.1 (2,551.27) 100 (100) Hex2-Hep2-GlcNAc-PEA2-Kdo2-lipid A*
MA-1 galE LOS A 2,266.4 (2,266.07) 32 (43) Hex-Hep2-GlcNAc-PEA1-Kdo2-lipid A*
LOS A′ 2,389.3 (2,389.12) 100 (100) Hex-Hep2-GlcNAc-PEA2-Kdo2-lipid A*
LOS B 2,427.8 (2,428.22) 20d (13) Hex2-Hep2-GlcNAc-PEA1-Kdo2-lipid A*
LOS B′ 2,551.7 (2,551.27) 11 (12) Hex2-Hep2-GlcNAc-PEA2-Kdo2-lipid A*
a

All molecular weights for O-deacylated LOS are reported from the MALDI data as their average mass values based on singly deprotonated charged molecular ions, (M − H)

b

Expressed as a percentage; determined from peak heights of the singly charged molecular ions for MALDI and of the doubly and triply charged ions for ESI. 

c

After O deacylation, the lipid A moiety is converted into diphosphoryl diacyl lipid A, containing two N-linked β-hydroxymyristic acid chains with an average Mr of 953.0. 

d

In the MALDI spectrum, this glycoform peak partially overlaps the potassium adduct of the molecular ion for the more abundant glycoform LOS A′ resulting in overestimation of this LOS B glycoform.