Eidgenössische Technische Hochschule (ETH) Zürich, Department of Biosystems Science and Engineering, 4058, Basel, Switzerland.
Swiss Institute of Bioinformatics (SIB), 4058, Basel, Switzerland.
Nat Commun. 2022 Jun 22;13(1):3483. doi: 10.1038/s41467-022-30781-y.
The regulation of cell growth has fundamental physiological, biotechnological and medical implications. However, methods that can continuously monitor individual cells at sufficient mass and time resolution hardly exist. Particularly, detecting the mass of individual microbial cells, which are much smaller than mammalian cells, remains challenging. Here, we modify a previously described cell balance ('picobalance') to monitor the proliferation of single cells of the budding yeast, Saccharomyces cerevisiae, under culture conditions in real time. Combined with optical microscopy to monitor the yeast morphology and cell cycle phase, the picobalance approaches a total mass resolution of 0.45 pg. Our results show that single budding yeast cells (S/G2/M phase) increase total mass in multiple linear segments sequentially, switching their growth rates. The growth rates weakly correlate with the cell mass of the growth segments, and the duration of each growth segment correlates negatively with cell mass. We envision that our technology will be useful for direct, accurate monitoring of the growth of single cells throughout their cycle.
细胞生长的调控具有重要的生理、生物技术和医学意义。然而,能够持续以足够的质量和时间分辨率监测单个细胞的方法几乎不存在。特别是,检测比哺乳动物细胞小得多的单个微生物细胞的质量仍然具有挑战性。在这里,我们修改了之前描述的细胞平衡(“picobalance”),以实时监测出芽酵母酿酒酵母单细胞的增殖情况。结合光学显微镜监测酵母形态和细胞周期阶段,picobalance 的总质量分辨率接近 0.45pg。我们的结果表明,单个出芽酵母细胞(S/G2/M 期)依次以多个线性片段增加总质量,切换其生长速率。生长速率与生长片段的细胞质量弱相关,并且每个生长片段的持续时间与细胞质量呈负相关。我们设想我们的技术将有助于直接、准确地监测整个细胞周期中单个细胞的生长。