ATP Consumption of Eukaryotic Flagella Measured at a Single-Cell Level

被引:51
作者
Chen, Daniel T. N. [1 ]
Heymann, Michael [1 ,2 ]
Fraden, Seth [1 ]
Nicastro, Daniela [3 ]
Dogic, Zvonimir [1 ]
机构
[1] Brandeis Univ, Martin Fisher Sch Phys, Waltham, MA 02254 USA
[2] Brandeis Univ, Grad Program Biophys & Struct Biol, Waltham, MA 02254 USA
[3] Brandeis Univ, Dept Biol, Waltham, MA 02254 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
INNER DYNEIN ARMS; SPERM FLAGELLA; CHLAMYDOMONAS-FLAGELLA; CRYOELECTRON TOMOGRAPHY; MOTOR DOMAIN; MOVEMENT; AXONEME; MICROTUBULES; OSCILLATION; MECHANISM;
D O I
10.1016/j.bpj.2015.11.003
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The motility of cilia and flagella is driven by thousands of dynein motors that hydrolyze adenosine triphosphate (ATP). Despite decades of genetic, biochemical, structural, and biophysical studies, some aspects of ciliary motility remain elusive, such as the regulation of beating patterns and the energetic efficiency of these nanomachines. In this study, we introduce an experimental method to measure ATP consumption of actively beating axonemes on a single-cell level. We encapsulated individual sea urchin sperm with demembranated flagellum inside water-in-oil emulsion droplets and measured the axoneme's ATP consumption by monitoring fluorescence intensity of a fluorophore-coupled reporter system for ATP turnover in the droplet. Concomitant phase contrast imaging allowed us to extract a linear dependence between the ATP consumption rate and the flagellar beating frequency, with similar to 2.3 x 10(5) ATP molecules consumed per beat of a demembranated flagellum. Increasing the viscosity of the aqueous medium led to modified beating waveforms of the axonemes and to higher energy consumption per beat cycle. Our single-cell experimental platform provides both new insights, to our knowledge, into the beating mechanism of flagella and a powerful tool for future studies.
引用
收藏
页码:2562 / 2573
页数:12
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