Mitochondrial function relies on the precise targeting and import of cytosolic proteins into mitochondrial subcompartments. Most matrix-targeted proteins follow the presequence pathway, which directs precursor proteins across the outer mitochondrial membrane (OMM) via the Translocase of the Outer Membrane (TOM) complex and into the matrix or inner mitochondrial membrane (IMM) via the Translocase of the Inner Membrane 23 (TIM23) complex. While classical biochemical studies provided detailed mechanistic insights into the composition and mechanism of the TIM23 complex, recent cryogenic-electron microscopy (cryo-EM) data challenge these established models and propose a revised model of translocation in which the TIM17 subunit acts as a ‘slide’ for precursor proteins, with Tim23 acting as a structural element. In this review, we summarize existing models, highlighting the questions and data needed to reconcile these perspectives, and enhance our understanding of TIM23 complex function.
Category: biotech/medical – Page 29
Researchers unveil a groundbreaking hydrogel that mimics human skin’s ability to heal itself rapidly, revolutionising medicine and artificial skin applications.
Geoffrey Canet et al. discover wakefulness body temperature upregulates neuronal tau secretion and correlates with tau levels, highlighting the importance of sleep and thermoregulation in Alzheimer’s disease:
The figure shows temperature-dependent increase of colocalization between SDC3 (purple) and TauC3 (yellow) in primary mouse cortical neurons.
1Centre de Recherche du CHU de Québec – Université Laval, Axe Neurosciences, Québec, Québec City, Canada.
2Université Laval, Faculté de Médecine, Département de Psychiatrie et Neurosciences, Québec, Québec City, Canada.
3Université Laval, Faculté de Médecine, Département de Médecine Moléculaire, Québec, Québec City, Canada.
University of California, Davis, researchers have developed a new, neuroplasticity-promoting drug closely related to LSD that harnesses the psychedelic’s therapeutic power with reduced hallucinogenic potential.
Researchers discovered an entirely new human blood type after solving a 50-year mystery.
Back in 1972, doctors were stumped when a pregnant woman’s blood sample was missing a surface molecule that was present on everyone else’s red blood cells at the time. No one could explain it.
Fast forward fifty years, and scientists believe to have sussed it. The discovery led researchers from the UK and Israel to describe a new blood group system in humans, publishing their findings in 2024.
More Americans are receiving computed tomography (CT) scans than ever before, and while this technology can save lives, some scientists are concerned about the potential for low doses of ionizing radiation to increase cancer risks.
(Spanish: [sanˈtjaɣo raˈmon i kaˈxal] ; 1 May 1852 – 17 October 1934) [ 1 ] [ 2 ] was a Spanish neuroscientist, pathologist, and histologist specializing in neuroanatomy and the central nervous system. He and Camillo Golgi received the Nobel Prize in Physiology or Medicine in 1906. [ 3 ] Ramón y Cajal was the first Spaniard to win a scientific Nobel Prize. His original investigations of the microscopic structure of the brain made him a pioneer of modern neuroscience.
Researchers at Children’s Hospital of Philadelphia (CHOP) developed a longitudinal atlas of neuroblastoma, a common and potentially deadly childhood cancer, to gain a deeper understanding into precise molecular mechanisms underlying why and how certain treatments eventually become ineffective.
The findings, which offer insights that could potentially lead to new personalized medicine approaches in neuroblastoma treatment, were published today in the journal Nature Genetics.
Despite significant advances in the standard of care, the 5-year survival rate of high-risk neuroblastoma after diagnosis remains less than 50%. Neuroblastoma cells within the same tumor can vary greatly, which creates challenges in treatment efficacy. Until now, the scientific community lacked understanding of how the tumor microenvironment changes during treatment.
Babies and young children may breathe and absorb plasticizers called phthalates, flame retardants, and other harmful chemicals from their mattresses while they sleep, according to a pair of studies published by the University of Toronto in Environmental Science & Technology and Environmental Science & Technology Letters. These chemicals are linked to neurological and reproductive problems, asthma, hormone disruption, and cancer.
“Sleep is vital for brain development, particularly for infants and toddlers. However, our research suggests that many mattresses contain chemicals that can harm kids’ brains,” says senior author Miriam Diamond, professor at the University of Toronto.
“This is a wake-up call for manufacturers and policymakers to ensure our children’s beds are safe and support healthy brain development.”
Researchers have discovered a type of “molecular glue” that can be used to inhibit certain pathological protein interactions. Their findings were published in the paper, “Molecular glues that inhibit deubiquitylase activity and inflammatory signaling,” in Nature Structural & Molecular Biology.
The Wistar Institute’s Joseph Salvino, Ph.D.—in collaboration with Elton Zeqiraj, Ph.D., of The University of Leeds and Roger Greenberg, M.D., Ph.D., of The Perelman School of Medicine at the University of Pennsylvania—led the study.
“Molecular glues are an exciting new area of research that allows us to fight disease by working with the body’s systems rather than against them,” said Dr. Salvino. “By gluing together an inactive form of the BRISC complex with our system, we’re able to reduce the continuous inflammatory signaling due to dysregulated BRISC complex activity in autoimmune diseases.”