A spatially resolved elemental nanodomain organization within acidocalcisomes in Trypanosoma cruzi

Author:

Girard-Dias Wendell1234,Augusto Ingrid123,V. A. Fernandes Tácio56,G. Pascutti Pedro5,de Souza Wanderley1237ORCID,Miranda Kildare1237ORCID

Affiliation:

1. Laboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-902, Brazil

2. Centro Nacional de Biologia Estrutural e Bioimagem, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-902, Brazil

3. Instituto Nacional de Ciência e Tecnologia em Biologia Estrutural e Bioimagem - Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-902, Brazil

4. Plataforma de Microscopia Eletrônica Rudolf Barth, Instituto Oswaldo Cruz - Fiocruz, Rio de Janeiro 21041-250, Brazil

5. Laboratório de Modelagem e Dinâmica Molecular, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-902, Brazil

6. Instituto de Tecnologia de Fármacos (Farmanguinhos), Fiocruz, Rio de Janeiro 22775-903, Brazil

7. Centro Multiusuário para Análise de Fenômenos Biomédicos, Universidade do Estado do Amazonas, Amazonas 69065-001, Brazil

Abstract

How are ions distributed in the three-dimensional (3D) volume confined in a nanoscale compartment? Regulation of ionic flow in the intracellular milieu has been explained by different theoretical models and experimentally demonstrated for several compartments with microscale dimensions. Most of these models predict a homogeneous distribution of ions seconds or milliseconds after an initial diffusion step formed at the ion translocation site, leaving open questions when it comes to ion/element distribution in spaces/compartments with nanoscale dimensions. Due to the influence of compartment size on the regulation of ionic flow, theoretical variations of classical models have been proposed, suggesting heterogeneous distributions of ions/elements within nanoscale compartments. Nonetheless, such assumptions have not been fully proven for the 3D volume of an organelle. In this work, we used a combination of cutting-edge electron microscopy techniques to map the 3D distribution of diffusible elements within the whole volume of acidocalcisomes in trypanosomes. Cryofixed cells were analyzed by scanning transmission electron microscopy tomography combined with elemental mapping using a high-performance setup of X-ray detectors. Results showed the existence of elemental nanodomains within the acidocalcisomes, where cationic elements display a self-excluding pattern. These were validated by Pearson correlation analysis and in silico molecular dynamic simulations. Formation of element domains within the 3D space of an organelle is demonstrated. Distribution patterns that support the electrodiffusion theory proposed for nanophysiology models have been found. The experimental pipeline shown here can be applied to a variety of models where ion mobilization plays a crucial role in physiological processes.

Funder

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. FhaA plays a key role in mycobacterial polar elongation and asymmetric growth;2024-08-13

2. Profile of Wanderley de Souza;Proceedings of the National Academy of Sciences;2024-04-15

3. Contribution of microscopy to a better understanding of the anatomy of pathogenic protists;Proceedings of the National Academy of Sciences;2024-04-15

4. Advances in the cellular biology, biochemistry, and molecular biology of acidocalcisomes;Microbiology and Molecular Biology Reviews;2023-12-15

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