TY - JOUR
T1 - Enhanced single-cell metabolomics by capillary electrophoresis electrospray ionization-mass spectrometry with field amplified sample injection
AU - Liao, Hsiao Wei
AU - Rubakhin, Stanislav
AU - Philip, Marina C.
AU - Sweedler, Jonathan V.
N1 - Funding was provided by the National Science Foundation by Award No. CHE-1606791 and the National Institute on Drug Abuse by Award No. P30 DA018310. This study was also supported by the Ministry of Science and Technology of Taiwan (MOST 106-2917-I-564-054). The National Resource for Aplysia (Miami, FL) is funded by PHS grant No. P40 OD010952. The content is solely the responsibility of the authors and does not necessarily represent the official views of the funding agencies.
Funding was provided by the National Science Foundation by Award No. CHE-1606791 and the National Institute on Drug Abuse by Award No. P30 DA018310 . This study was also supported by the Ministry of Science and Technology of Taiwan ( MOST 106-2917-I-564-054 ). The National Resource for Aplysia (Miami, FL) is funded by PHS grant No. P40 OD010952 . The content is solely the responsibility of the authors and does not necessarily represent the official views of the funding agencies.
PY - 2020/6/29
Y1 - 2020/6/29
N2 - Single-cell metabolomics provides information on the biochemical state of an individual cell and its relationship with the surrounding environment. Characterization of metabolic cellular heterogeneity is challenging, in part due to the small amounts of analytes and their wide dynamic concentration ranges within individual cells. CE-ESI-MS is well suited to single-cell assays because of its low sample-volume requirements and low detection limits. While the volume of a cell is in the picoliter range, after isolation, the typical volume of the lysed cell sample is on the order of a microliter; however, only nanoliters are injected into the CE system, with the volume mismatch limiting analytical performance. Here we developed an approach for the detection of intracellular metabolites from a single neuron using field amplified sample injection (FASI) CE-ESI-MS. Through the application of FASI, we achieved 100- to 300-fold detection limit enhancement compared to hydrodynamic injections. We further enhanced the analyte identification and quantification accuracy via introduction of two internal standards. As a result, the relative standard deviations of migration times were reduced to <5%, aiding identification. Finally, we successfully applied FASI CE-ESI-MS to the untargeted profiling of metabolites of Aplysia californica pleural sensory neurons with <50 μm diameter cell somata. As a result, twenty one neurotransmitters and metabolites have been quantified in these neurons.
AB - Single-cell metabolomics provides information on the biochemical state of an individual cell and its relationship with the surrounding environment. Characterization of metabolic cellular heterogeneity is challenging, in part due to the small amounts of analytes and their wide dynamic concentration ranges within individual cells. CE-ESI-MS is well suited to single-cell assays because of its low sample-volume requirements and low detection limits. While the volume of a cell is in the picoliter range, after isolation, the typical volume of the lysed cell sample is on the order of a microliter; however, only nanoliters are injected into the CE system, with the volume mismatch limiting analytical performance. Here we developed an approach for the detection of intracellular metabolites from a single neuron using field amplified sample injection (FASI) CE-ESI-MS. Through the application of FASI, we achieved 100- to 300-fold detection limit enhancement compared to hydrodynamic injections. We further enhanced the analyte identification and quantification accuracy via introduction of two internal standards. As a result, the relative standard deviations of migration times were reduced to <5%, aiding identification. Finally, we successfully applied FASI CE-ESI-MS to the untargeted profiling of metabolites of Aplysia californica pleural sensory neurons with <50 μm diameter cell somata. As a result, twenty one neurotransmitters and metabolites have been quantified in these neurons.
KW - Capillary electrophoresis electrospray ionization-mass spectrometry
KW - Field amplified sample injection
KW - Single-cell metabolomics
UR - https://www.scopus.com/pages/publications/85083878022
UR - https://www.scopus.com/pages/publications/85083878022#tab=citedBy
U2 - 10.1016/j.aca.2020.04.028
DO - 10.1016/j.aca.2020.04.028
M3 - Article
C2 - 32418602
AN - SCOPUS:85083878022
SN - 0003-2670
VL - 1118
SP - 36
EP - 43
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
ER -