The Biogenesis Process of VDAC - From Early Cytosolic Events to Its Final Membrane Integration.

Front Physiol

Interfaculty Institute of Biochemistry, University of Tübingen, Tübingen, Germany.

Published: August 2021

Voltage dependent anion-selective channel (VDAC) is the most abundant protein in the mitochondrial outer membrane. It is a membrane embedded β-barrel protein composed of 19 mostly anti-parallel β-strands that form a hydrophilic pore. Similar to the vast majority of mitochondrial proteins, VDAC is encoded by nuclear DNA, and synthesized on cytosolic ribosomes. The protein is then targeted to the mitochondria while being maintained in an import competent conformation by specific cytosolic factors. Recent studies, using yeast cells as a model system, have unearthed the long searched for mitochondrial targeting signal for VDAC and the role of cytosolic chaperones and mitochondrial import machineries in its proper biogenesis. In this review, we summarize our current knowledge regarding the early cytosolic stages of the biogenesis of VDAC molecules, the specific targeting of VDAC to the mitochondrial surface, and the subsequent integration of VDAC into the mitochondrial outer membrane by the TOM and TOB/SAM complexes.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8388839PMC
http://dx.doi.org/10.3389/fphys.2021.732742DOI Listing

Publication Analysis

Top Keywords

early cytosolic
8
mitochondrial outer
8
outer membrane
8
vdac mitochondrial
8
vdac
7
mitochondrial
6
cytosolic
5
biogenesis process
4
process vdac
4
vdac early
4

Similar Publications

Epigenetic therapies facilitate transcription of immunogenic repetitive elements that cull cancer cells through 'viral mimicry' responses. Paradoxically, cancer-initiating events also facilitate transcription of repetitive elements. Contributions of repetitive element transcription towards cancer initiation, and the mechanisms by which cancer cells evade lethal viral mimicry responses during tumor initiation remain poorly understood.

View Article and Find Full Text PDF

Hotspots for Disease-Causing Mutations in the Mitochondrial TIM23 Import Complex.

Genes (Basel)

November 2024

School of Neurobiology, Biochemistry and Biophysics, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 6997801, Israel.

The human mitochondrial proteome comprises approximately 1500 proteins, with only 13 being encoded by mitochondrial DNA. The remainder are encoded by the nuclear genome, translated by cytosolic ribosomes, and subsequently imported into and sorted within mitochondria. The process of mitochondria-destined protein import is mediated by several intricate protein complexes distributed among the four mitochondrial compartments.

View Article and Find Full Text PDF

Magnetic control of membrane damage in early endosomes using internalized magnetic nanoparticles.

Cell Struct Funct

December 2024

Graduate Course in Biological Sciences, Division of Science and Engineering, Graduate School of Arts and Sciences, Iwate University.

Article Synopsis
  • The study explores how membrane stiffness affects cell behavior and examines the physical properties of membranes in a lab setting.
  • Researchers introduced magnetic nanoparticles into breast cancer cells and used magnetic fields to see if they could damage the endosomal membrane.
  • Findings show that applying a strong static magnetic field can induce membrane damage in early endosomes, particularly when using a magnetic field strength of 100 mT for five minutes, highlighting the potential for controlled damage with magnetic fields.
View Article and Find Full Text PDF

Manganese is a potent inducer of lysosomal activity that inhibits de novo HBV infection.

PLoS Pathog

January 2025

Key Laboratory of Medical Molecular Virology (MOE/NHC/CAMS), Shanghai Institute of Infectious Disease and Biosecurity, School of Basic Medical Sciences, Fudan University, Shanghai, China.

Sodium taurocholate co-transporting polypeptide (NTCP) has been identified as an entry receptor for hepatitis B virus (HBV), but the molecular events of the viral post-endocytosis steps remain obscure. In this study, we discovered that manganese (Mn) could strongly inhibit HBV infection in NTCP-reconstituted HepG2 cells without affecting viral replication. We therefore profiled the antiviral effects of Mn2+ in an attempt to elucidate the regulatory mechanisms involved in early HBV infection.

View Article and Find Full Text PDF

In plants, cellular function is orchestrated by three distinct genomes located within the nucleus, mitochondrion, and plastid. These genomes are interdependent, requiring tightly coordinated maintenance and expression. Plastids host several multisubunit protein complexes encoded by both the plastid and nuclear genomes.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!