High-resolution mass spectrometric analysis reveals structural insights into vitamin B12 impurities, suggesting improved quantification methods.
Vitamin B12 is one of nature's most structurally complex small molecules and an essential coenzyme that is only produced by prokaryotes. Due to its pivotal role in nerve function, metabolism, and the immune system in humans, vitamin B12 deficiency is considered a major public health concern. Numerous mass spectrometric analytical methods exist to identify and quantify vitamin B12 from a wide array of matrices, including food, diet supplements, tissues, and plasma. Nevertheless, structural elucidation of vitamin B12 through tandem mass spectrometry (MS/MS) fragmentation remains a challenge due to its intricate structure, versatility of derivatives, and isobaric impurities. This work combined native and force-degraded samples with synthetic impurity standards to elucidate the structures of collision-induced dissociation (CID) fragment ions of vitamin B12 over the full m/z range with a high mass accuracy. Our findings show that the complexity of vitamin B12 MS/MS fragments can be deduced through a "simple" combination of four (4) major CID cleavage sites. These results enabled us to propose a general vitamin B12 CID fragmentation pathway that allows for the calculation of the theoretical m/z for fragment ions of unknown cobalamin species and impurities. This work aims to provide a novel, universal analytical platform to identify and quantify vitamin B12 and its derivatives through mass spectrometry with high mass accuracy.
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Gessmann et al. (2025) studied this question.
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