On the mechanism and functional significance of the ADP/ATP carrier (AAC) dimerization


Цитировать

Полный текст

Открытый доступ Открытый доступ
Доступ закрыт Доступ предоставлен
Доступ закрыт Только для подписчиков

Аннотация

According to previous studies, ADP/ATP carrier (AAC) can possibly exist as a monomer or in a dimer state in the inner mitochondrial membrane; however, the question on its functional oligomeric state is still open. The aim of the present work is to establish the external factors that could control the functional oligomeric state of AAC (i.e., monomer or dimer). The study is based on the results of our previous work, which revealed that the volume regulation system of mitochondria (MVRS) affects the oxidative phosphorylation (OXPHOS) system: MVRS could transfer OXPHOS system functioning in a state of supercomplex. Consequently, one may expect that the volume regulation system could also control the functional state of AAC during phosphorylation. Here, on rat liver mitochondria we show that, depending on the incubation medium tonicity, AAC functions in two different ways: either as a monomer (in hypotonic and isotonic media) or as a dimer (in a hypertonic medium). Thus, the transition between the monomeric and dimeric forms of AAC is regulated by MVRS, as well as by functioning of OXPHOS. We conclude that the structural reorganization of AAC is associated with the entire OXPHOS reorganization into a supercomplex. It was also found that dimerization of AAC can occur not only due to the action of MVRS (in hypotonic media) but also under hypoxic conditions.

Об авторах

V. Moiseeva

Institut de Biologie Structurale (IBS), University Grenoble Alpes, CEA

Email: yag@genebee.msu.su
Франция, Grenoble, 38044

T. Murugova

Frank Laboratory of Neutron Physics; Moscow Institute of Physics and Technology

Email: yag@genebee.msu.su
Россия, Dubna, 141980; Dolgoprudny, 141701

I. Vangeli

Belozersky Institute of Physico-Chemical Biology

Email: yag@genebee.msu.su
Россия, Moscow, 119992

I. Byvshev

Moscow Institute of Physics and Technology

Email: yag@genebee.msu.su
Россия, Dolgoprudny, 141701

S. Ravaud

Institut de Biologie Structurale (IBS), University Grenoble Alpes, CEA

Email: yag@genebee.msu.su
Франция, Grenoble, 38044

R. Simonyan

Belozersky Institute of Physico-Chemical Biology

Email: yag@genebee.msu.su
Россия, Moscow, 119992

V. Gordeliy

Institut de Biologie Structurale (IBS), University Grenoble Alpes, CEA; Moscow Institute of Physics and Technology; Institute of Complex Systems (ICS), ICS-6: Structural Biochemistry

Email: yag@genebee.msu.su
Франция, Grenoble, 38044; Dolgoprudny, 141701; Juelich, 52425

E. Pebay-Peyroula

Institut de Biologie Structurale (IBS), University Grenoble Alpes, CEA

Email: yag@genebee.msu.su
Франция, Grenoble, 38044

L. Yaguzhinsky

Moscow Institute of Physics and Technology; Belozersky Institute of Physico-Chemical Biology

Автор, ответственный за переписку.
Email: yag@genebee.msu.su
Россия, Dolgoprudny, 141701; Moscow, 119992

Дополнительные файлы

Доп. файлы
Действие
1. JATS XML

© Pleiades Publishing, Ltd., 2017

Согласие на обработку персональных данных

 

Используя сайт https://journals.rcsi.science, я (далее – «Пользователь» или «Субъект персональных данных») даю согласие на обработку персональных данных на этом сайте (текст Согласия) и на обработку персональных данных с помощью сервиса «Яндекс.Метрика» (текст Согласия).