高等学校化学学报 ›› 2014, Vol. 35 ›› Issue (1): 37.doi: 10.7503/cjcu20130721
魏王慧1, 王青1, 储艳秋1(), 汪日志2(
), 丁传凡1
收稿日期:
2013-07-25
出版日期:
2014-01-10
发布日期:
2013-12-13
作者简介:
联系人简介: 储艳秋, 男, 博士, 副教授, 主要从事质谱法研究有机分子和生物大分子及其相互作用的研究. E-mail:基金资助:
WEI Wanghui1, WANG Qing1, CHU Yanqiu1,*(), WANG Rizhi2,*(
), DING Chuanfan1
Received:
2013-07-25
Online:
2014-01-10
Published:
2013-12-13
Contact:
CHU Yanqiu,WANG Rizhi
E-mail:chuyq@fudan.edu.cn;rizhi9752@hotmail.com
Supported by:
摘要:
为了探索金属离子对含有不同侧链的多肽气相解离的影响, 采用质谱法研究了碱金属离子Li+, Na+, K+, Rb+和Cs+分别与丝氨酸、 亮氨酸和赖氨酸五肽(分别简写为S5, L5和K5)形成的复合物的裂解反应. 质谱定性结果表明, 5种碱金属离子均可以在气相中与丝氨酸、 亮氨酸和赖氨酸五肽形成配合比为1∶1 和2∶1的非共价复合物; 竞争反应结果表明, 随着碱金属离子半径的增加, 它们与3种五肽的结合能力逐渐减弱. 质谱定量结果表明, K+与丝氨酸、 亮氨酸和赖氨酸五肽复合物的结合常数分别为8.94×104, 2.83×104和2.50×103 L/mol, 表明K+与五肽复合物的结合强度按照丝氨酸、 亮氨酸和赖氨酸的顺序依次减小. 含不同侧链碱金属离子-五肽复合物的碰撞诱导解离结果表明, 复合物的碎裂主要发生在骨架上, 丝氨酸五肽复合物最易碎裂, 亮氨酸五肽复合物其次, 赖氨酸五肽复合物则较难碎裂, 且3种复合物的侧链断裂情况也呈现明显差异. 此外, 研究了Na+与亮氨酸五肽复合物所产生的碎片离子, 分析了不同离子之间的来源关系, 并以Dunbar的复合物理论模型为依据, 推测在碎裂过程中, 碱金属离子可能向五肽的碳端或氮端偏移. 质谱碎片分析结果表明, 在2∶1的非共价复合物中, 第一个碱金属离子与五肽上4个酰胺键的羰基结合, 第二个碱金属离子与五肽的羧基氧原子结合.
中图分类号:
TrendMD:
魏王慧, 王青, 储艳秋, 汪日志, 丁传凡. 气相中碱金属离子与丝氨酸、 亮氨酸和赖氨酸五肽复合物的裂解反应. 高等学校化学学报, 2014, 35(1): 37.
WEI Wanghui, WANG Qing, CHU Yanqiu, WANG Rizhi, DING Chuanfan. Fragmentation Reactions of Complexes of Alkali Metal Ions with Pentaserine, Pentaleucine and Pentalysine in Gas Phase†. Chem. J. Chinese Universities, 2014, 35(1): 37.
Fig.1 Mass spectra for competition reaction of pentapeptides with alkali metal ions in a molar ratio of 1∶1∶1∶1∶1∶1∶1(A) G5; (B) S5; (C) L5; (D) K5. c(Pentapeptide)=c(Alkali metal ion)=1.0×10-4 mol/L.
105 [G | 105 [K+]0/(mol·L-1) | IP | IPM | IPM2 | a1 | a2 | 10-5 Ka1/(L·mol-1) |
---|---|---|---|---|---|---|---|
5.00 | 10.00 | 7.54 | 100.00 | 97.94 | 0.487 | 0.477 | 4.84 |
5.00 | 15.00 | 3.17 | 100.00 | 98.03 | 0.497 | 0.487 | 4.06 |
5.00 | 20.00 | 1.92 | 100.00 | 98.35 | 0.499 | 0.491 | 3.96 |
5.00 | 25.00 | 1.68 | 100.00 | 98.42 | 0.499 | 0.492 | 3.15 |
5.00 | 30.00 | 1.32 | 100.00 | 99.31 | 0.498 | 0.495 | 3.15 |
Average | 3.83 | ||||||
SD | 0.70 | ||||||
RSD(%) | 18.2 |
Table 1 Ka1 values of the complexes of G5 with K+
105 [G | 105 [K+]0/(mol·L-1) | IP | IPM | IPM2 | a1 | a2 | 10-5 Ka1/(L·mol-1) |
---|---|---|---|---|---|---|---|
5.00 | 10.00 | 7.54 | 100.00 | 97.94 | 0.487 | 0.477 | 4.84 |
5.00 | 15.00 | 3.17 | 100.00 | 98.03 | 0.497 | 0.487 | 4.06 |
5.00 | 20.00 | 1.92 | 100.00 | 98.35 | 0.499 | 0.491 | 3.96 |
5.00 | 25.00 | 1.68 | 100.00 | 98.42 | 0.499 | 0.492 | 3.15 |
5.00 | 30.00 | 1.32 | 100.00 | 99.31 | 0.498 | 0.495 | 3.15 |
Average | 3.83 | ||||||
SD | 0.70 | ||||||
RSD(%) | 18.2 |
105 [S | 105 [K+]0/(mol·L-1) | IP | IPM | IPM2 | a1 | a2 | 10-4 |
---|---|---|---|---|---|---|---|
5.00 | 10.00 | 23.99 | 100.00 | 51.09 | 0.571 | 0.292 | 9.86 |
5.00 | 15.00 | 12.80 | 100.00 | 70.47 | 0.546 | 0.384 | 9.25 |
5.00 | 20.00 | 8.15 | 100.00 | 97.10 | 0.487 | 0.473 | 9.49 |
5.00 | 25.00 | 6.97 | 100.00 | 97.57 | 0.489 | 0.477 | 8.09 |
5.00 | 30.00 | 5.47 | 100.00 | 98.15 | 0.491 | 0.482 | 8.00 |
Average | 8.94 | ||||||
SD | 0.84 | ||||||
RSD(%) | 9.4 |
Table 2 Ka1 values of the complexes of S5 with K+
105 [S | 105 [K+]0/(mol·L-1) | IP | IPM | IPM2 | a1 | a2 | 10-4 |
---|---|---|---|---|---|---|---|
5.00 | 10.00 | 23.99 | 100.00 | 51.09 | 0.571 | 0.292 | 9.86 |
5.00 | 15.00 | 12.80 | 100.00 | 70.47 | 0.546 | 0.384 | 9.25 |
5.00 | 20.00 | 8.15 | 100.00 | 97.10 | 0.487 | 0.473 | 9.49 |
5.00 | 25.00 | 6.97 | 100.00 | 97.57 | 0.489 | 0.477 | 8.09 |
5.00 | 30.00 | 5.47 | 100.00 | 98.15 | 0.491 | 0.482 | 8.00 |
Average | 8.94 | ||||||
SD | 0.84 | ||||||
RSD(%) | 9.4 |
105 [L | 105 [K+]0/(mol·L-1) | IP | IPM | IPM2 | a1 | a2 | 10-4 |
---|---|---|---|---|---|---|---|
5.00 | 10.00 | 51.03 | 100.00 | 8.19 | 0.628 | 0.051 | 3.08 |
5.00 | 15.00 | 33.63 | 100.00 | 13.53 | 0.680 | 0.092 | 2.79 |
5.00 | 20.00 | 21.85 | 100.00 | 15.31 | 0.729 | 0.112 | 3.01 |
5.00 | 25.00 | 18.68 | 100.00 | 17.09 | 0.737 | 0.126 | 2.68 |
5.00 | 30.00 | 15.71 | 100.00 | 20.75 | 0.733 | 0.152 | 2.57 |
Average | 2.83 | ||||||
SD | 0.21 | ||||||
RSD(%) | 7.4 |
Table 3 Ka1 values of the complexes of L5 with K+
105 [L | 105 [K+]0/(mol·L-1) | IP | IPM | IPM2 | a1 | a2 | 10-4 |
---|---|---|---|---|---|---|---|
5.00 | 10.00 | 51.03 | 100.00 | 8.19 | 0.628 | 0.051 | 3.08 |
5.00 | 15.00 | 33.63 | 100.00 | 13.53 | 0.680 | 0.092 | 2.79 |
5.00 | 20.00 | 21.85 | 100.00 | 15.31 | 0.729 | 0.112 | 3.01 |
5.00 | 25.00 | 18.68 | 100.00 | 17.09 | 0.737 | 0.126 | 2.68 |
5.00 | 30.00 | 15.71 | 100.00 | 20.75 | 0.733 | 0.152 | 2.57 |
Average | 2.83 | ||||||
SD | 0.21 | ||||||
RSD(%) | 7.4 |
105 [K | 105 [K+]0/(mol·L-1) | IP | IPM | IPM2 | a1 | a2 | 10-3 |
---|---|---|---|---|---|---|---|
5.00 | 10.00 | 100.00 | 22.88 | 7.29 | 0.176 | 0.056 | 2.68 |
5.00 | 15.00 | 100.00 | 34.33 | 14.11 | 0.231 | 0.095 | 2.66 |
5.00 | 20.00 | 100.00 | 42.90 | 22.47 | 0.259 | 0.136 | 2.47 |
5.00 | 25.00 | 100.00 | 51.93 | 31.90 | 0.282 | 0.174 | 2.37 |
5.00 | 30.00 | 100.00 | 61.13 | 40.60 | 0.303 | 0.201 | 2.31 |
Average | 2.50 | ||||||
SD | 0.17 | ||||||
RSD(%) | 6.8 |
Table 4 Ka1 values of the complexes of K5 with K+
105 [K | 105 [K+]0/(mol·L-1) | IP | IPM | IPM2 | a1 | a2 | 10-3 |
---|---|---|---|---|---|---|---|
5.00 | 10.00 | 100.00 | 22.88 | 7.29 | 0.176 | 0.056 | 2.68 |
5.00 | 15.00 | 100.00 | 34.33 | 14.11 | 0.231 | 0.095 | 2.66 |
5.00 | 20.00 | 100.00 | 42.90 | 22.47 | 0.259 | 0.136 | 2.47 |
5.00 | 25.00 | 100.00 | 51.93 | 31.90 | 0.282 | 0.174 | 2.37 |
5.00 | 30.00 | 100.00 | 61.13 | 40.60 | 0.303 | 0.201 | 2.31 |
Average | 2.50 | ||||||
SD | 0.17 | ||||||
RSD(%) | 6.8 |
Fig.2 Relationship between intensity of mass spectrometric peak and normalized collision energy The precursors are the complexes of G5(■), S5(●), L5(▲) or K5(◆) with H+(A), Li+(B) and 2Li+(C).
Fig.4 CID breakdown curves for the complexes of Na+ with pentaleucinea. Precursor ion [L5+Na]+; b. [b4+Na+OH]+; c. [b4+Na-H]+; d. [y3+Na+H]+; e. [b3+Na-H]+; f. [y2+Na+H]+.
Precursor ion(#) | an/an*/an** | Other | ||
---|---|---|---|---|
[S5+H]+ | a4, a3, a2, a1, a4-H2O, a4-2H2O, a3-H2O, a3-2H2O, a2-H2O | b4, b3, b2, b4-H2O, b3-H2O, b2-H2O, b3-2H2O | y3, y2, y1 | [#-H2O]+, [#-2H2O]+, [#-3H2O]+, [#-4H2O]+ |
[S5+Li]+ | a4*, a4*-CH2O, a4*-H2O, a3*, a3*-CH2O, a3*-H2O, a2*, a2*-CH2O, a2*-H2O, a1* | [b4+Li+OH]+, [b4+Li+OH- CH2O]+, b4*-H2O, b4*-CO2, [b3+Li+OH]+, b4*-H2O-CH2O, b3*-H2O, b4*, b3*-CO2, [b3+ Li+OH-CH2O]+, b3*, b2*, b3*-H2O-CH2O, b2*-H2O, b2*-H2O-CH2O | y2*, y2*-H2O, y1* | [#-H2O]+, [#-CH2O]+, [#-H2O-CH2O]+ , [#-H2O-CO2]+, [#-H2O-2CH2O]+, [#-2H2O-CH2O]+ |
[S5+Na]+ | a4*, a4*-CH2O, a3*, a1* | [b4+Na+OH]+, [b4+Na+OH- CH2O]+, b4*, b4*-H2O, [b3+ Na+OH]+, b3*, b2*, [b3+Na+ OH-CH2O]+ | y2* | [#-H2O]+, [#-CH2O]+, [#-H2O-CH2O]+, [#-H2O-CO2]+ |
[S5+K]+ | a4*, a4*-CH2O | [b4+K+OH]+, [b4+K+OH- CH2O]+, b4*, b4*-H2O, [b3+ K+OH]+, [b3+K+OH-CH2O]+, b3* | K+, [#-H2O]+, [#-CH2O]+, [#-2CH2O]+ | |
[S5+Rb]+ | Rb+ | |||
[S5+Cs]+ | Cs+ | |||
[S5+2Li-H]+ | a4**, a3**, a4*, a3* | b3**, b3**-CH2O, b2**, b2**-CH2O | y4**, y3**, y2**, y1**, y4**-CH2O, y3**-CH2O, y2**-CH2O, y1**-CH2O, y4**-2CH2O, y3**-CH2O | [#-H2O]+, [#-CH2O]+, [#-2CH2O]+, [#-3CH2O]+, [#-4CH2O]+, [#-H2O-CH2O]+, [#-H2O-2CH2O]+, [#-H2O-3CH2O]+, [#-2H2O-3CH2O]+ |
[S5+2Na-H]+ | a4**-CH2O, a4**-2CH2O, a4**-3CH2O, a3**-CH2O | b2**, b4*, b4*-CH2O | y4**, y3**, y2**, y1**, y4**-CH2O, y3**-CH2O, y2**-CH2O, y1**-CH2O, y3**-2CH2O, y2**-2CH2O | [#-H2O]+, [#-CH2O]+, [#-2CH2O]+, [#- 3CH2O]+, [#-4CH2O]+, [#-5CH2O]+, [#-H2O- CH2O]+, [#-H2O- 2CH2O]+, [#-H2O- 3CH2O]+, [#-H2O- 4CH2O]+ |
[S5+2K-H]+ | a4**-H2O | b3**-CH2O, b3**-2CH2O, b2**-CH2O | y4**, y3**, y2**, y1**, y3**-CH2O, y2**-CH2O, y1**-CH2O, y2**-2CH2O | K+, [#-H2O]+, [#-2H2O]+, [#-CH2O]+, [#-2CH2O]+, [#-3CH2O]+, [#-4CH2O]+, [#-H2O-CH2O]+, [#-H2O-2CH2O]+, [#-2H2O- 2CH2O]+, [#-H2O- 3CH2O]+, [#-2H2O- 3CH2O]+, [#-H2O- 4CH2O]+ |
[S5+2Rb-H]+ | a4**, a4**-H2O | b3**, b1**, b3**-2H2O | y4**, y3**, y2**, y1** | Rb+, [#-H2O]+, [#-CH2O]+, [#-2CH2O]+, [#-3CH2O]+, [#-H2O- CH2O]+, [#-H2O-2CH2O]+ |
[S5+2Cs-H]+ | a4**-H2O | b3** | y4**, y3**, y1**, y1**-CH2O | Cs+, [#-H2O]+, [#-CH2O]+, [#-2CH2O]+, [#-H2O-CH2O]+, [#-H2O-2CH2O]+, [#-3CH2O]+ |
Table 5 Main fragment ions of protonated and alkali metal cationized S5 complexes obtained with CID
Precursor ion(#) | an/an*/an** | Other | ||
---|---|---|---|---|
[S5+H]+ | a4, a3, a2, a1, a4-H2O, a4-2H2O, a3-H2O, a3-2H2O, a2-H2O | b4, b3, b2, b4-H2O, b3-H2O, b2-H2O, b3-2H2O | y3, y2, y1 | [#-H2O]+, [#-2H2O]+, [#-3H2O]+, [#-4H2O]+ |
[S5+Li]+ | a4*, a4*-CH2O, a4*-H2O, a3*, a3*-CH2O, a3*-H2O, a2*, a2*-CH2O, a2*-H2O, a1* | [b4+Li+OH]+, [b4+Li+OH- CH2O]+, b4*-H2O, b4*-CO2, [b3+Li+OH]+, b4*-H2O-CH2O, b3*-H2O, b4*, b3*-CO2, [b3+ Li+OH-CH2O]+, b3*, b2*, b3*-H2O-CH2O, b2*-H2O, b2*-H2O-CH2O | y2*, y2*-H2O, y1* | [#-H2O]+, [#-CH2O]+, [#-H2O-CH2O]+ , [#-H2O-CO2]+, [#-H2O-2CH2O]+, [#-2H2O-CH2O]+ |
[S5+Na]+ | a4*, a4*-CH2O, a3*, a1* | [b4+Na+OH]+, [b4+Na+OH- CH2O]+, b4*, b4*-H2O, [b3+ Na+OH]+, b3*, b2*, [b3+Na+ OH-CH2O]+ | y2* | [#-H2O]+, [#-CH2O]+, [#-H2O-CH2O]+, [#-H2O-CO2]+ |
[S5+K]+ | a4*, a4*-CH2O | [b4+K+OH]+, [b4+K+OH- CH2O]+, b4*, b4*-H2O, [b3+ K+OH]+, [b3+K+OH-CH2O]+, b3* | K+, [#-H2O]+, [#-CH2O]+, [#-2CH2O]+ | |
[S5+Rb]+ | Rb+ | |||
[S5+Cs]+ | Cs+ | |||
[S5+2Li-H]+ | a4**, a3**, a4*, a3* | b3**, b3**-CH2O, b2**, b2**-CH2O | y4**, y3**, y2**, y1**, y4**-CH2O, y3**-CH2O, y2**-CH2O, y1**-CH2O, y4**-2CH2O, y3**-CH2O | [#-H2O]+, [#-CH2O]+, [#-2CH2O]+, [#-3CH2O]+, [#-4CH2O]+, [#-H2O-CH2O]+, [#-H2O-2CH2O]+, [#-H2O-3CH2O]+, [#-2H2O-3CH2O]+ |
[S5+2Na-H]+ | a4**-CH2O, a4**-2CH2O, a4**-3CH2O, a3**-CH2O | b2**, b4*, b4*-CH2O | y4**, y3**, y2**, y1**, y4**-CH2O, y3**-CH2O, y2**-CH2O, y1**-CH2O, y3**-2CH2O, y2**-2CH2O | [#-H2O]+, [#-CH2O]+, [#-2CH2O]+, [#- 3CH2O]+, [#-4CH2O]+, [#-5CH2O]+, [#-H2O- CH2O]+, [#-H2O- 2CH2O]+, [#-H2O- 3CH2O]+, [#-H2O- 4CH2O]+ |
[S5+2K-H]+ | a4**-H2O | b3**-CH2O, b3**-2CH2O, b2**-CH2O | y4**, y3**, y2**, y1**, y3**-CH2O, y2**-CH2O, y1**-CH2O, y2**-2CH2O | K+, [#-H2O]+, [#-2H2O]+, [#-CH2O]+, [#-2CH2O]+, [#-3CH2O]+, [#-4CH2O]+, [#-H2O-CH2O]+, [#-H2O-2CH2O]+, [#-2H2O- 2CH2O]+, [#-H2O- 3CH2O]+, [#-2H2O- 3CH2O]+, [#-H2O- 4CH2O]+ |
[S5+2Rb-H]+ | a4**, a4**-H2O | b3**, b1**, b3**-2H2O | y4**, y3**, y2**, y1** | Rb+, [#-H2O]+, [#-CH2O]+, [#-2CH2O]+, [#-3CH2O]+, [#-H2O- CH2O]+, [#-H2O-2CH2O]+ |
[S5+2Cs-H]+ | a4**-H2O | b3** | y4**, y3**, y1**, y1**-CH2O | Cs+, [#-H2O]+, [#-CH2O]+, [#-2CH2O]+, [#-H2O-CH2O]+, [#-H2O-2CH2O]+, [#-3CH2O]+ |
Precursor ion(#) | an/ | Other | ||
---|---|---|---|---|
[L5+H]+ | a4, a2, a1, a4-NH3, a3-NH3, a4-CH2-CH-(CH3)2 | b3, b2 | y4, y3, y2 | [#-H2O]+ |
[L5+Li]+ | a4*, a3*, a3*-(CH3)2, a4*- CH2-CH-(CH3)2, a2*, a2*-(CH3)2 | [b4+Li+OH]+, b4*-NH3, [b3+Li+OH]+, b3*-NH3, b4*, b3*, b2* | y3*, y2*, y1* | [#-H2O-NH3]+ |
[L5+Na]+ | a4*, a3*, a1*, a3*-CH2-CH- (CH3)2, a2*-CH2-CH-(CH3)2 | [b4+Na+OH]+, b3*, [b3+Na+OH]+, b2* | y2*, y1* | |
[L5+K]+ | a4*, a3* | [b4+K+OH]+, b4*, [b3+K+OH]+ | y2*, y2*-NH3, y4*-CO | K+, [#-CO]+, [#-CO2]+ |
[L5+Rb]+ | [b4+Rb+OH]+ | Rb+ | ||
[L5+Cs]+ | Cs+ | |||
[L5+2Li-H]+ | a4**, a3**, a4*, a3*, a1*, a3*-CO2, a2*-CO2 | b2*, b4*-H2O-NH3, b3*-H2O-NH3 | y4**, y2**, y1**, y3*, y1* | [#-CO2]+, [#-H2O-NH3]+ |
[L5+2Na-H]+ | a4**, a4*, a3*, a2*, a1*, a3*-H2O-NH3, a2*-H2O-NH3, a2*-CH2-CH-(CH3)2 | b3*, b3*-NH3 | y4**, y3**, y2**, y1**, y2**-CO2 | [#-CO2]+ |
[L5+2K-H]+ | a4*, a3*, a2*, a1*-(CH3)2 | y4**, y3**, y2**, y1**, y1**-H2O-NH3 | K+ | |
[L5+2Rb-H]+ | a3**-CH2-CH-(CH3)2, a2**-CH2-CH-(CH3)2 | y3**, y2**, y1**, y3**-NH3 | Rb+ | |
[L5+2Cs-H]+ | a2**-CH2-CH-(CH3)2 | y3**, y2**, y1**, y4**-CH2-CH-(CH3)2 | Cs+ |
Table 6 Main product ions of protonated and alkali metal cationized L5 complexes obtained with CID
Precursor ion(#) | an/ | Other | ||
---|---|---|---|---|
[L5+H]+ | a4, a2, a1, a4-NH3, a3-NH3, a4-CH2-CH-(CH3)2 | b3, b2 | y4, y3, y2 | [#-H2O]+ |
[L5+Li]+ | a4*, a3*, a3*-(CH3)2, a4*- CH2-CH-(CH3)2, a2*, a2*-(CH3)2 | [b4+Li+OH]+, b4*-NH3, [b3+Li+OH]+, b3*-NH3, b4*, b3*, b2* | y3*, y2*, y1* | [#-H2O-NH3]+ |
[L5+Na]+ | a4*, a3*, a1*, a3*-CH2-CH- (CH3)2, a2*-CH2-CH-(CH3)2 | [b4+Na+OH]+, b3*, [b3+Na+OH]+, b2* | y2*, y1* | |
[L5+K]+ | a4*, a3* | [b4+K+OH]+, b4*, [b3+K+OH]+ | y2*, y2*-NH3, y4*-CO | K+, [#-CO]+, [#-CO2]+ |
[L5+Rb]+ | [b4+Rb+OH]+ | Rb+ | ||
[L5+Cs]+ | Cs+ | |||
[L5+2Li-H]+ | a4**, a3**, a4*, a3*, a1*, a3*-CO2, a2*-CO2 | b2*, b4*-H2O-NH3, b3*-H2O-NH3 | y4**, y2**, y1**, y3*, y1* | [#-CO2]+, [#-H2O-NH3]+ |
[L5+2Na-H]+ | a4**, a4*, a3*, a2*, a1*, a3*-H2O-NH3, a2*-H2O-NH3, a2*-CH2-CH-(CH3)2 | b3*, b3*-NH3 | y4**, y3**, y2**, y1**, y2**-CO2 | [#-CO2]+ |
[L5+2K-H]+ | a4*, a3*, a2*, a1*-(CH3)2 | y4**, y3**, y2**, y1**, y1**-H2O-NH3 | K+ | |
[L5+2Rb-H]+ | a3**-CH2-CH-(CH3)2, a2**-CH2-CH-(CH3)2 | y3**, y2**, y1**, y3**-NH3 | Rb+ | |
[L5+2Cs-H]+ | a2**-CH2-CH-(CH3)2 | y3**, y2**, y1**, y4**-CH2-CH-(CH3)2 | Cs+ |
Precursor ion(#) | an/ | Other | ||
---|---|---|---|---|
[K5+H]+ | a4-(CH2)4-NH2, a3-(CH2)4-NH2, a1, a1-NH3 | b4, b3, b2, b1, b4-H2O, b3-H2O, b2-H2O, b4-H2O-NH3, b4-H2O-2NH3, b3-H2O-NH3, b3-H2O-2NH3, b2-H2O-NH3, b2-H2O-2NH3 | y4, y3, y2, y1 | [#-H2O]+ |
[K5+Li]+ | a1*, a2*- (CH2)4-NH2 | [b4+Li+OH]+, b4*, b3*, b2*, b1*, b4*-H2O, b4*-H2O-NH3, [b3+Li+OH]+, b3*-H2O, b3*-H2O-NH3, b2*-H2O, b2*-H2O-NH3 | y2*, y1* | [#-H2O]+ |
[K5+Na]+ | a1*, a3*- (CH2)4-NH2 | [b4+Na+OH]+, b4*, b3*, b2*, b1*, b4*-H2O, b2*-H2O-NH3, [b3+Na+OH]+, b3*-H2O | y4*-CO2, y2*, y1* | [#-H2O]+ |
[K5+K]+ | a2* | [b4+K+OH]+, b4*, b3*, b2*, b1*, b3*-H2O, b2*-H2O, [b3+K+OH]+ | y2*, y1*, y1*-(CH2)4 | K+, [#-H2O]+, [#-CO2]+ |
[K5+Rb]+ | [b4+Rb+OH]+ | Rb+ | ||
[K5+Cs]+ | [b4+Cs+OH]+ | Cs+ | ||
[K5+2Li-H]+ | a4**, a3**, a2**, a2**-H2O-NH3, a1* | b3**, b2**, b4*, b3*, b1* | y4**, y3**, y2**, y1**, y4*, y1* | [#-CO2]+, [#-CO2-CH2-NH2]+ |
[K5+2Na-H]+ | a4**, a4**-4CH2 | b4**, b4**-CO2, b4*, b3*, b2* | y4**, y3**, y2**, y1**, y3**-CO2, y2**-CO2, y4*, y3*, y2*, y1*, y1**-4CH2 | [#-CO2]+ |
[K5+2K-H]+ | a2**, a2**- (CH2)4-NH2 | b4* | y4**, y3**, y2**, y1**, y4*, y3* | K+, [#-CO2]+ |
[K5+2Rb-H]+ | b4* | y3**, y2**, y1**, y3* | Rb+ | |
[K5+2Cs-H]+ | b4* | y3**, y2**, y1** | Cs+ |
Table 7 Main product ions of protonated and alkali metal cationized K5 complexes obtained with CID
Precursor ion(#) | an/ | Other | ||
---|---|---|---|---|
[K5+H]+ | a4-(CH2)4-NH2, a3-(CH2)4-NH2, a1, a1-NH3 | b4, b3, b2, b1, b4-H2O, b3-H2O, b2-H2O, b4-H2O-NH3, b4-H2O-2NH3, b3-H2O-NH3, b3-H2O-2NH3, b2-H2O-NH3, b2-H2O-2NH3 | y4, y3, y2, y1 | [#-H2O]+ |
[K5+Li]+ | a1*, a2*- (CH2)4-NH2 | [b4+Li+OH]+, b4*, b3*, b2*, b1*, b4*-H2O, b4*-H2O-NH3, [b3+Li+OH]+, b3*-H2O, b3*-H2O-NH3, b2*-H2O, b2*-H2O-NH3 | y2*, y1* | [#-H2O]+ |
[K5+Na]+ | a1*, a3*- (CH2)4-NH2 | [b4+Na+OH]+, b4*, b3*, b2*, b1*, b4*-H2O, b2*-H2O-NH3, [b3+Na+OH]+, b3*-H2O | y4*-CO2, y2*, y1* | [#-H2O]+ |
[K5+K]+ | a2* | [b4+K+OH]+, b4*, b3*, b2*, b1*, b3*-H2O, b2*-H2O, [b3+K+OH]+ | y2*, y1*, y1*-(CH2)4 | K+, [#-H2O]+, [#-CO2]+ |
[K5+Rb]+ | [b4+Rb+OH]+ | Rb+ | ||
[K5+Cs]+ | [b4+Cs+OH]+ | Cs+ | ||
[K5+2Li-H]+ | a4**, a3**, a2**, a2**-H2O-NH3, a1* | b3**, b2**, b4*, b3*, b1* | y4**, y3**, y2**, y1**, y4*, y1* | [#-CO2]+, [#-CO2-CH2-NH2]+ |
[K5+2Na-H]+ | a4**, a4**-4CH2 | b4**, b4**-CO2, b4*, b3*, b2* | y4**, y3**, y2**, y1**, y3**-CO2, y2**-CO2, y4*, y3*, y2*, y1*, y1**-4CH2 | [#-CO2]+ |
[K5+2K-H]+ | a2**, a2**- (CH2)4-NH2 | b4* | y4**, y3**, y2**, y1**, y4*, y3* | K+, [#-CO2]+ |
[K5+2Rb-H]+ | b4* | y3**, y2**, y1**, y3* | Rb+ | |
[K5+2Cs-H]+ | b4* | y3**, y2**, y1** | Cs+ |
[1] | Li Y., Lin H. Q., Deng C. H., Yang P. Y., Zhang X. M., Proteomics, 2008, 8(2), 238—345 |
[2] | Xu Y. W., Zhang L. J., Lu H. J., Yang P. Y., Anal. Chem., 2008, 80(21), 8324—8328 |
[3] | Zhou M., McDonald J. F., Fernandez F. M., J. Am. Soc. Mass Spectrom., 2010, 21(1), 68—75 |
[4] | Chen C., Chu Y. Q., Dai X. H., Fang X., Ding C. F., Acta Phys. Chim. Sin., 2013, 29(6), 1336—1343 |
(陈琛, 储艳秋, 戴新华, 方向, 丁传凡.物理化学学报, 2013,29(6), 1336—1343) | |
[5] | Halim V. A., Muck A., Hartl M., Ibanez A. Z., Giri A., Proteomics, 2009 , 9(1) , 171—181 |
[6] | Wilson J.J., Brodbelt J. S., Anal.Chem.,2007, 79,2067—2077 |
[7] | Biemann K., Methods Enzymol., 1990, 193, 455—460 |
[8] | Good D. M., Wenger C. D., Coon J. J., Proteomics, 2010, 10(1), 164—167 |
[9] | Spengler B., J. Mass. Spectrom., 1997, 32, 1019—1036 |
[10] | Qin Y. J., Wei S. G., Wang X. L., Yang F., Wang B., Guo X. H., Chem. J. Chinese Universities, 2011, 32(8), 2748—2756 |
(秦玉娇, 魏士刚, 王晓录, 杨帆, 汪兵, 国新华.高等学校化学学报, 2011,32(8), 2748—2756) | |
[11] | Wysocki V. H., Smith L. L., Breci L. A., J. Mass Spectrom., 2000, 35, 1399—1406 |
[12] | Harrison A. G., Mass Spectrom. Rev., 2009, 28(4), 640—654 |
[13] | Knapp-Mohammady M., Young A. B., Paizs B., Harrison A.G., J. Am. Soc. Mass Spectrom., 2009, 20(11), 2135—2143 |
[14] | Paizs B., Suhai S., Mass Spectrom. Rev., 2005, 24(4), 508—548 |
[15] | Bythell B. J., Somogyi A., Paizs B., J. Am. Soc. Mass Spectrom., 2009, 20(4), 618—624 |
[16] | Cydzik M., Rudowska M., Stefanowicz P., Szewczuk Z., J. Am. Soc. Mass Spectrom., 2011, 22(12), 2013—2107 |
[17] | Shields S. L., Bluhm B. K., Russell D. H., J. Am. Soc. Mass Spectrom., 2000, 11, 626—633 |
[18] | Pingitore F., Wesdemiotis C., Anal. Chem., 2005, 77, 1796—1803 |
[19] | Russell D. H., Mass Spectrom. Rev., 1986, 5, 167—189 |
[20] | Tang X., Ens W., Standing K. G., Westmore J. B., Anal. Chem., 1988, 60, 1791—1799 |
[21] | Teesch L. M., Adams J., J. Am. Chem. Soc., 1990, 112, 4110—4120 |
[22] | Teesch L. M., Orlando R. C., Adams J., J. Am. Chem. Soc., 1991, 113, 3668—3675 |
[23] | Crizer D. M., Xia Y., McLuckey S. A., J. Am. Soc. Mass Spectrom., 2009, 20(9), 1718—1722 |
[24] | Zhang H. R., Chen G., Wang L., Ding L., Tian Y., Jin W. J., Zhang H. Q., Int. J. Mass Spectrom., 2006, 252(1), 1—10 |
[25] | Chu Y. Q., Dai X. H., Jiang D., Fang X., Ding C. F., Rapid Commun. Mass Spectrom., 2010, 24, 2255—2262 |
[26] | Guo C., Hu N., Jiang K. Z., Chen W. X., Wang X. X., Pan Y. J., Rapid Commun. Mass Spectrom., 2010, 24, 409—414 |
[27] | Dunbar R. C., Polfer N. C., Berden G., Oomens J. , Int. J. Mass Spectrom., 2012, 330, 71—77 |
[28] | Dunbar R. C., Steill J. D., Polfer N. C., Oomens J., J. Phys. Chem. A, 2013, 117(6), 1094—1101 |
[29] | Pu D., Vincent J. B., Cassady C. J., J. Mass Spectrom., 2008, 43, 773—781 |
[30] | Wang Q., Chu Y. Q., Zhang K., Dai X. H., Fang X., Ding C. F., Acta Phys. Chim. Sin., 2012, 28, 971—978 |
(王青, 储艳秋, 张开, 戴新华, 方向, 丁传凡.物理化学学报, 2012, 28, 971—978) |
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