TY - JOUR
T1 - Highly sensitive and high-throughput analysis of plant hormones using ms-probe modification and liquid chromatographytandem mass spectrometry
T2 - An application for hormone profiling in oryza sativa
AU - Kojima, Mikiko
AU - Kamada-Nobusada, Tomoe
AU - Komatsu, Hirokazu
AU - Takei, Kentaro
AU - Kuroha, Takeshi
AU - Mizutani, Masaharu
AU - Ashikari, Motoyuki
AU - Ueguchi-Tanaka, Miyako
AU - Matsuoka, Makoto
AU - Suzuki, Koji
AU - Sakakibara, Hitoshi
PY - 2009/7
Y1 - 2009/7
N2 - We have developed a highly sensitive and high-throughput method for the simultaneous analysis of 43 molecular species of cytokinins, auxins, ABA and gibberellins. This method consists of an automatic liquid handling system for solid phase extraction and ultra-performance liquid chromatography (UPLC) coupled with a tandem quadrupole mass spectrometer (qMS/MS) equipped with an electrospray interface (ESI; UPLC-ESI-qMS/MS). In order to improve the detection limit of negatively charged compounds, such as gibberellins, we chemically derivatized fractions containing auxin, ABA and gibberellins with bromocholine that has a quaternary ammonium functional group. This modification, that we call 'MS-probe', makes these hormone derivatives have a positive ion charge and permits all compounds to be measured in the positive ion mode with UPLC-ESI-qMS/MS in a single run. Consequently, quantification limits of gibberellins increased up to 50-fold. Our current method needs <100 mg (FW) of plant tissues to determine phytohormone profiles and enables us to analyze >180 plant samples simultaneously. Application of this method to plant hormone profiling enabled us to draw organ distribution maps of hormone species in rice and also to identify interactions among the four major hormones in the rice gibberellin signaling mutants, gid1-3, gid2-1 and slr1. Combining the results of hormone profiling data with transcriptome data in the gibberellin signaling mutants allows us to analyze relationships between changes in gene expression and hormone metabolism.
AB - We have developed a highly sensitive and high-throughput method for the simultaneous analysis of 43 molecular species of cytokinins, auxins, ABA and gibberellins. This method consists of an automatic liquid handling system for solid phase extraction and ultra-performance liquid chromatography (UPLC) coupled with a tandem quadrupole mass spectrometer (qMS/MS) equipped with an electrospray interface (ESI; UPLC-ESI-qMS/MS). In order to improve the detection limit of negatively charged compounds, such as gibberellins, we chemically derivatized fractions containing auxin, ABA and gibberellins with bromocholine that has a quaternary ammonium functional group. This modification, that we call 'MS-probe', makes these hormone derivatives have a positive ion charge and permits all compounds to be measured in the positive ion mode with UPLC-ESI-qMS/MS in a single run. Consequently, quantification limits of gibberellins increased up to 50-fold. Our current method needs <100 mg (FW) of plant tissues to determine phytohormone profiles and enables us to analyze >180 plant samples simultaneously. Application of this method to plant hormone profiling enabled us to draw organ distribution maps of hormone species in rice and also to identify interactions among the four major hormones in the rice gibberellin signaling mutants, gid1-3, gid2-1 and slr1. Combining the results of hormone profiling data with transcriptome data in the gibberellin signaling mutants allows us to analyze relationships between changes in gene expression and hormone metabolism.
KW - ABA
KW - Auxins
KW - Cytokinins
KW - Gibberellins
KW - Mass spectrometry
KW - Oryza sativa
UR - http://www.scopus.com/inward/record.url?scp=67651085448&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=67651085448&partnerID=8YFLogxK
U2 - 10.1093/pcp/pcp057
DO - 10.1093/pcp/pcp057
M3 - Article
C2 - 19369275
AN - SCOPUS:67651085448
SN - 0032-0781
VL - 50
SP - 1201
EP - 1214
JO - Plant and Cell Physiology
JF - Plant and Cell Physiology
IS - 7
ER -