The
complementary use of single cell atomic mass spectrometry (MS)
and ambient molecular MS allowed for the in-depth study of arsenate
uptake by Chlamydomonas reinhardtii cells and of
the effect this toxic metalloid species has on their lipid profile.
Compared to conventional inductively coupled plasma mass spectrometry
(ICP–MS) analysis, in which case hundreds of thousands of cells
are digested and then analyzed, it is demonstrated that single cell
(SC) ICP–MS provides uptake data that are potentially of greater
biological relevance. This includes the arsenic mass distribution
within the cell population, which fits to a log-normal probability
function, the most frequently contained arsenic mass within the cells
(1.5–1.8 fg As per cell), and the mean arsenic uptake value
(ranging from 2.7 to 4.1 fg As per cell for the three arsenate incubation
concentrations, that is, 15, 22.5, and 30 μg As per mL) derived
from the log-normal arsenic mass distribution within the cell population.
The SC approach also allows for differentiating the arsenic present
in and/or adsorbed on the cells, from the arsenic present in the extracellular
solution, in a single analysis. In a similar fashion, ambient molecular
MS in the form of desorption easy ambient sonic spray ionization (EASI)
-MS was used to rapidly profile cell membrane lipids from cells spotted
directly on a glass slide. EASI–MS analysis revealed that cells
grown in the presence of increasing concentrations of arsenate exhibited
changes in the degree of saturation of their membrane lipids, as was
observed by the increasing intensity ratio of lipids with less unsaturated
acyl chains to the same type of lipids with more unsaturated fatty
acid chains. Thus, indicating “homeoviscous adaptation”
of extraplastidial and thylakoid cell membranes, induced by the presence
of arsenate.