Department of Chemistry, Indiana University, 800 East Kirkwood Avenue, Bloomington, IN, 47405, USA.
Pre-Pivotal Drug Product Technologies, Amgen Inc., Thousand Oaks, CA, 91320, USA.
J Am Soc Mass Spectrom. 2016 Dec;27(12):2041-2053. doi: 10.1007/s13361-016-1487-9. Epub 2016 Sep 9.
Six ion fragmentation techniques that can distinguish aspartic acid from its isomer, isoaspartic acid, were compared. MALDI post-source decay (PSD), MALDI 157 nm photodissociation, tris(2,4,6-trimethoxyphenyl)phosphonium bromide (TMPP) charge tagging in PSD and photodissociation, ESI collision-induced dissociation (CID), electron transfer dissociation (ETD), and free-radical initiated peptide sequencing (FRIPS) with CID were applied to peptides containing either aspartic or isoaspartic acid. Diagnostic ions, such as the y-46 and b+HO, are present in PSD, photodissociation, and charge tagging. c+57 and z-57 ions are observed in ETD and FRIPS experiments. For some molecules, aspartic and isoaspartic acid yield ion fragments with significantly different intensities. ETD and charge tagging appear to be most effective at distinguishing these residues. Graphical Abstract ᅟ.
六种可以区分天冬氨酸与其异构体异天冬氨酸的离子碎裂技术进行了比较。基质辅助激光解吸/电离后源衰退(MALDI PSD)、MALDI 157nm 光解、MALDI PSD 和光解中的三(2,4,6-三甲氧基苯基)膦溴化盐(TMPP)电荷标记、电喷雾碰撞诱导解离(ESI CID)、电子转移解离(ETD)和自由基引发肽测序(FRIPS)与 CID 均应用于含有天冬氨酸或异天冬氨酸的肽。在 PSD、光解和电荷标记中存在 y-46 和 b+HO 等诊断离子。在 ETD 和 FRIPS 实验中观察到 c+57 和 z-57 离子。对于某些分子,天冬氨酸和异天冬氨酸产生的离子碎片强度有明显差异。ETD 和电荷标记似乎最能有效地区分这些残基。