Nanita Sergio C, Takats Zoltan, Cooks R Graham, Myung Sunnie, Clemmer David E
Department of Chemistry, Purdue University, West Lafayette, Indiana 47907, USA.
J Am Soc Mass Spectrom. 2004 Sep;15(9):1360-5. doi: 10.1016/j.jasms.2004.06.010.
Chiral enrichment of serine is achieved in experiments that involve formation of serine octamers starting from non-racemic serine solutions. Serine octamers were generated by means of electrospray and sonic spray ionization of aqueous solutions of d(3)-L-serine (108 Da) and D-serine (105 Da) having different molar ratios of enantiomers. A cyclic process involving the formation of chirally-enriched octameric cluster ions and their dissociation, viz. Ser(1) --> Ser(8) --> Ser(1), allows serine monomers to be regenerated with increased enantiomeric excess as shown in two types of experiments: (1) Chiral enrichment in serine was observed in MS/MS/MS experiments in a quadrupole ion trap in which the entire distribution of serine octamers formed from non-racemic solutions was isolated, collisionally activated, and fragmented. Monomeric serine was regenerated with increased enantiomeric excess upon dissociation of octamers when compared with the enantiomeric composition of the original solution. (2) Chiral enrichment was observed in the products of soft-landing of mass-selected protonated serine octamers. These ions were generated by means of electrospray or sonic spray ionization, mass selected, and collected on a gold surface using ion soft-landing. Chiral enrichment of the soft-landed serine was established by redissolving the recovered material and comparing the intensities of protonated molecular ions of d(3)-L-serine and D-serine after APCI-MS analysis. Both of these experiments showed comparable results, suggesting that formation of serine octamers depends only on the enantiomeric composition of the serine solution and that the magnitude of the chiral preference is intrinsic to octamers formed from solutions of given chiral composition.
丝氨酸的手性富集是在一些实验中实现的,这些实验涉及从非外消旋丝氨酸溶液开始形成丝氨酸八聚体。通过对具有不同对映体摩尔比的d(3)-L-丝氨酸(108 Da)和D-丝氨酸(105 Da)的水溶液进行电喷雾和超声喷雾电离来生成丝氨酸八聚体。一个涉及形成手性富集的八聚体簇离子及其解离的循环过程,即Ser(1)→Ser(8)→Ser(1),使得丝氨酸单体能够以增加的对映体过量再生,如两种类型的实验所示:(1)在四极杆离子阱中的MS/MS/MS实验中观察到丝氨酸的手性富集,在该实验中,从非外消旋溶液形成的丝氨酸八聚体的整个分布被分离、碰撞激活并碎片化。与原始溶液的对映体组成相比,八聚体解离时单体丝氨酸以增加的对映体过量再生。(2)在质量选择的质子化丝氨酸八聚体软着陆的产物中观察到手性富集。这些离子通过电喷雾或超声喷雾电离产生,进行质量选择,并使用离子软着陆收集在金表面上。通过将回收的材料重新溶解并比较APCI-MS分析后d(3)-L-丝氨酸和D-丝氨酸的质子化分子离子强度,确定了软着陆丝氨酸的手性富集。这两个实验都显示了可比的结果,表明丝氨酸八聚体的形成仅取决于丝氨酸溶液的对映体组成,并且手性偏好的程度对于由给定手性组成的溶液形成的八聚体来说是固有的。