A matrix ATP requirement for presequence translocation across the inner membrane of mitochondria.
نویسندگان
چکیده
The mitochondrial presequence initiates protein translocation across the inner membrane of mitochondria in a delta psi-dependent step. We have investigated the role of matrix ATP in this process. When matrix ATP was reduced to interfere with the function of mitochondrial heat shock protein 70, presequence translocation across the inner membrane was strongly inhibited. This was accompanied by the accumulation of an import intermediate that was unprocessed and accessible to protease added to the intact mitochondria. Both delta psi and matrix ATP were required for further translocation of this intermediate into the matrix. When ATP levels are insufficient to support protein import, it appears that the presequence becomes translocated across the inner membrane, but delta psi does not maintain it in the matrix. Presequence translocation across the inner membrane is thus a reversible reaction, and a step dependent on matrix ATP is required to make it unidirectional. Based on these observations, a model on the role of delta psi, mthsp70, and matrix ATP in presequence translocation across the inner membrane is presented.
منابع مشابه
The interactions of signal sequences with membranes.
brane [ZO], thereby contributing to the specific targeting of mitochondrial precursor proteins to mitochondria. Secondly, it can be imagined that the specific way of insertion of the presequence into the inner membrane is required in order to be correctly oriented for the subsequent action of the proteinaceous import machinery of the inner membrane and/or that of the membrane potential present ...
متن کاملInteraction of a synthetic mitochondrial presequence with isolated yeast mitochondria: mechanism of binding and kinetics of import.
The mechanism of interaction of a presequence with isolated yeast mitochondria was examined. A synthetic peptide corresponding to a matrix-targeting signal was covalently labeled with a fluorescent probe. Binding of the presequence to the surface of the mitochondria and translocation of the presequence into the interior of the mitochondria could then be monitored directly in solution by measuri...
متن کاملTrypanosoma brucei cytochrome c1 is imported into mitochondria along an unusual pathway.
In most eukaryotic organisms, cytochrome c(1) is encoded in the nucleus, translated on cytosolic ribosomes, and directed to its final destination in the mitochondrial inner membrane by a bipartite, cleaved, amino-terminal presequence. However, in the kinetoplastids and euglenoids, the cytochrome c(1) protein has been shown to lack a cleaved presequence; a single methionine is removed from the a...
متن کاملThe sorting route of cytochrome b2 branches from the general mitochondrial import pathway at the preprotein translocase of the inner membrane.
Cytochrome b2 is synthesized in the cytosol with a bipartite presequence. The first part of the presequence targets the protein to mitochondria and mediates translocation into the mitochondrial matrix compartment; the second part contains the sorting signal that is required for delivery of the protein to the intermembrane space. The localization of the structures that recognize the sorting sign...
متن کاملProtein Translocation into the Intermembrane Space and Matrix of Mitochondria: Mechanisms and Driving Forces
Mitochondria contain two aqueous subcompartments, the matrix and the intermembrane space (IMS). The matrix is enclosed by both the inner and outer mitochondrial membranes, whilst the IMS is sandwiched between the two. Proteins of the matrix are synthesized in the cytosol as preproteins, which contain amino-terminal matrix targeting sequences that mediate their translocation through translocases...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Journal of biological chemistry
دوره 268 32 شماره
صفحات -
تاریخ انتشار 1993