Three-Minute Enantioselective Amino Acid Analysis by Ultra-High-Performance Liquid Chromatography Drift Tube Ion Mobility-Mass Spectrometry Using a Chiral Core-Shell Tandem Column Approach.
Simon Jonas JaagYounes ValadbeigiTim J CausonHarald GrossMichael LämmerhoferPublished in: Analytical chemistry (2024)
Fast liquid chromatography (LC) amino acid enantiomer separation of 6-aminoquinolyl- N -hydroxysuccinimidyl carbamate (AQC) derivatives using a chiral core-shell particle tandem column with weak anion exchange and zwitterionic-type quinine carbamate selectors in less than 3 min was achieved. Enantiomers of all AQC-derivatized proteinogenic amino acids and some isomeric ones (24 in total plus achiral glycine) were baseline separated ( R s > 1.5 except for glutamic acid with R s = 1.3), while peaks of distinct amino acids and structural isomers (constitutional isomers and diastereomers of leucine and threonine) of the same configuration overlapped to various degrees. For this reason, drift tube ion mobility-mass spectrometry was added (i.e., LC-IM-MS) as an additional selectivity filter without extending run time. The IM separation dimension in combination with high-resolution demultiplexing enabled confirmation of threonine isomers (threonine, allo -threonine, homoserine), while leucine, isoleucine, and allo -isoleucine have almost identical collisional cross-section ( DT CCS N2 ) values and added no selectivity to the partial LC separation. Density functional theory (DFT) calculations show that IM separation of threonine isomers was possible due to conformational stabilization by hydrogen bond formation between the hydroxyl side chain and the urea group. Generally, the CCS N2 of protonated ions increased uniformly with addition of the AQC label, while outliers could be explained by consideration of intramolecular interactions and additional structural analysis. Preliminary validation of the enantioselective LC-IM-MS method for quantitative analysis showed compliance of accuracy and precision with common limits in bioanalytical methods, and applicability to a natural lipopeptide and a therapeutic synthetic peptide could be demonstrated.
Keyphrases
- liquid chromatography
- mass spectrometry
- amino acid
- capillary electrophoresis
- tandem mass spectrometry
- ultra high performance liquid chromatography
- density functional theory
- high resolution mass spectrometry
- simultaneous determination
- protein kinase
- high resolution
- high performance liquid chromatography
- molecular dynamics
- gas chromatography
- solid phase extraction
- ionic liquid
- molecular dynamics simulations
- multiple sclerosis
- quantum dots