2018
DOI: 10.1021/jacs.8b07864
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Accurate Quantification of N-Glycolylneuraminic Acid in Therapeutic Proteins Using Supramolecular Mass Spectrometry

Abstract: Practical applications of innovative host-guest systems are challenging because of unexpected guest competitors and/or subtle environmental differences. Herein, a supramolecular mass spectrometry (MS)-based method using a synthetic host, cucurbit[7]uril (CB[7]), was developed for identifying and quantifying N-glycolylneuraminic acid (Neu5Gc) in therapeutic glycoproteins, which critically reduces drug efficacy. The development of a reliable derivatization-free analytical method for Neu5Gc is highly challenging … Show more

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Cited by 12 publications
(13 citation statements)
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“…It is worth mentioning that these techniques are not able to distinguish various types of sialic acids, such as Neu5Ac and Neu5Gc. Due to the immunogenic effects of the non-human Neu5Gc, a second complementary approach should be applied to characterize sialic acids [117,118]. This approach often includes the chemical release of sialic acid from the glycans and fluorescent labeling with DMB, prior RPLC chromatography with FD detection [119].…”
Section: Glycan Analysis and Sialic Acids Contentmentioning
confidence: 99%
“…It is worth mentioning that these techniques are not able to distinguish various types of sialic acids, such as Neu5Ac and Neu5Gc. Due to the immunogenic effects of the non-human Neu5Gc, a second complementary approach should be applied to characterize sialic acids [117,118]. This approach often includes the chemical release of sialic acid from the glycans and fluorescent labeling with DMB, prior RPLC chromatography with FD detection [119].…”
Section: Glycan Analysis and Sialic Acids Contentmentioning
confidence: 99%
“…The FIDI‐MS setup is presented in Figure S1. Mass spectrometry has a notable history in the study of host–guest chemistry, and it can provide detailed, fingerprint information on the reaction products. Collectively, FIDI‐MS has proven to be an excellent means to examine oxidation chemistry at the air–water interface.…”
Section: Figurementioning
confidence: 99%
“…CB[6] has been modified by substituting the locations denoted by “R” with 2-(butylamino)­ethanethiol, and the resulting cucurbituril derivative disrupts the cellular membranes in a number of bacterial species . Several CB­[ n ] complexes also traverse cellular membranes, making CB­[ n ]­s potentially useful in selective drug delivery. CB­[ n ]­s have also been utilized for inducing protein dimerization; separating and quantifying sialic acid species; catalyzing oxidation, , hydrolysis, and ring formation reactions; and altering the photophysical properties of both the ground , and excited , states of guests for chemosensing experiments.…”
Section: Introductionmentioning
confidence: 99%