TY - JOUR
T1 - Mass selective ion transfer and accumulation in ion trap arrays
AU - Wang, Yuzhuo
AU - Zhang, Xiaohua
AU - Zhai, Yanbing
AU - Jiang, You
AU - Fang, Xiang
AU - Zhou, Mingfei
AU - Deng, Yulin
AU - Xu, Wei
N1 - Publisher Copyright:
© 2014 American Chemical Society.
PY - 2014/10/21
Y1 - 2014/10/21
N2 - The concept and method for mass selective ion transfer and accumulation within quadrupole ion trap arrays have been demonstrated. Proof-of-concept experiments have been performed on two sets of ion trap arrays: (1) a linear ion trap with axial ion ejection plus a linear ion trap with radial ion ejection; (2) a linear ion trap with axial ion ejection plus a linear ion trap with axial ion ejection. In both sets of ion trap arrays, ions trapped in the first ion trap could be mass selectively transferred and accumulated into the second ion trap, while keeping other ions reserved in the first ion trap. Different operating modes have been implemented and tested, including transferring all ions, ions within a selected mass range, ions with a mass-to-charge ratio of 1, and randomly selected ions. Unit mass resolution for ion transfer and ∼90% ion transfer efficiency has been achieved. A new tandem mass spectrometry scheme for analyzing multiple precursor ions in a single sample injection has been demonstrated, which would improve instrument duty cycle and sample utilization rate (especially for very limited samples), potentially facilitate applications like single cell analyses, and improve electron transfer dissociation efficiency.
AB - The concept and method for mass selective ion transfer and accumulation within quadrupole ion trap arrays have been demonstrated. Proof-of-concept experiments have been performed on two sets of ion trap arrays: (1) a linear ion trap with axial ion ejection plus a linear ion trap with radial ion ejection; (2) a linear ion trap with axial ion ejection plus a linear ion trap with axial ion ejection. In both sets of ion trap arrays, ions trapped in the first ion trap could be mass selectively transferred and accumulated into the second ion trap, while keeping other ions reserved in the first ion trap. Different operating modes have been implemented and tested, including transferring all ions, ions within a selected mass range, ions with a mass-to-charge ratio of 1, and randomly selected ions. Unit mass resolution for ion transfer and ∼90% ion transfer efficiency has been achieved. A new tandem mass spectrometry scheme for analyzing multiple precursor ions in a single sample injection has been demonstrated, which would improve instrument duty cycle and sample utilization rate (especially for very limited samples), potentially facilitate applications like single cell analyses, and improve electron transfer dissociation efficiency.
UR - http://www.scopus.com/inward/record.url?scp=84910666514&partnerID=8YFLogxK
U2 - 10.1021/ac502583b
DO - 10.1021/ac502583b
M3 - Article
AN - SCOPUS:84910666514
SN - 0003-2700
VL - 86
SP - 10164
EP - 10170
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 20
ER -