AI Article Synopsis

  • This study showcases a new technique using charge-detection quadrupole ion trap mass spectrometry to measure the dry masses of various mammalian and poultry red blood cells (RBCs) through laser-induced acoustic desorption.
  • Eight types of RBCs were analyzed, with weights ranging from 0.58 x 10^13 Da (9.6 pg) for goat cells to 2.80 x 10^13 Da (46.5 pg) for chicken cells, and human RBC masses varied depending on health conditions.
  • The mass distribution profiles were mostly near-Gaussian, indicating size variations, especially in anemic cells, suggesting that this method can be used effectively for rapid mass analysis of RBCs and other

Article Abstract

Herein, we report an application of charge-detection quadrupole ion trap mass spectrometry to the measurement of total dry masses of mammalian and poultry erythrocytes evaporated/ionized by laser-induced acoustic desorption. The method is rapid and widely applicable. Eight different types of red blood cells (RBCs) have been successfully analyzed, including those of human, goat, cow, mouse, pig, and chicken. The measured mean masses (weights per corpuscle) range from 0.58 x 10(13) Da (9.6 pg) of goat RBCs to 2.80 x 10(13) Da (46.5 pg) of chicken RBCs. The total dry weights determined for human RBCs from a healthy male adult, a patient with iron-deficiency anemia, and a patient with thalassemia are 34.8, 28.8, and 20.6 pg, respectively. These weights, except that of thalassemia, are all approximately 10% higher than their corresponding mean corpuscular hemoglobin values determined by a commercial automated hematology analyzer. The mass distribution profiles of the cells are all near-Gaussian, with a standard deviation of 15% for the normal human RBCs. The deviation increases significantly to 20% for RBCs with thalassemia characteristics and 27% for RBCs with iron-deficiency anemia characteristics. All the observations are in accord with their corresponding mean corpuscular volume measurements, indicating an increase in anisocytosis (variation in RBC size) in the anemic samples. Our results suggest a broad and promising application of this new technology to high-speed mass analysis of RBCs and other biological whole cells as well.

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http://dx.doi.org/10.1021/ac071207eDOI Listing

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