Copper dishomeostasis causes a misbalance in Catecholamine levels

Copper serves as a signaling and regulatory molecule as well as a cofactor of important enzymes in the brain, and is thus required for proper brain development and functioning. Irregularities in copper metabolism can lead to several disorders, including Menkes disease and Wilson’s disease. Menkes disease is the result of genetic mutations altering ATP7A, a … Read more

Using CRISPR/Cas9 to correct a Wilson’s Disease Mutation in Human Cells

Wilson’s Disease (WD) is a liver disease caused by mutations in a protein responsible for copper excretion. That protein, ATPase7B (ATP7B), is a pump that helps move copper in liver cells, and mutations in it cause it to lose its ability to function. The impaired excretion of copper from the liver leads to the accumulation … Read more

Chromium Allergy and its Activation of the Innate Immune Response

Chromium allergy is a type of allergic contact dermatitis characterized by rashes, inflammation, and scaling. Our innate immune response drives this inflammatory reaction when the surface of our skin comes in contact with chromium (hence, the term, “allergic contact dermatitis.”) The primary cause of chromium allergy is constant exposure to chromium-containing chemicals or compounds. The … Read more

Structural and biochemical analysis of the metallo-β-lactamase L1 from emerging pathogen Stenotrophomonas maltophilia revealed the subtle but distinct di-metal scaffold for catalytic activity

The emergence of antibiotic resistance is a major challenge in the clinical setting. Stenotrophomonas maltophilia is an emerging gram-negative bacterium that produces Metallo-b-lactamase (MBL) L1. Metallo-beta-Lactamases (MBLs) is a class B β-lactamases that hydrolyze β-lactam antibiotics. The β-lactam antibiotics, which include antibiotics such as penicillin, inhibit bacterial transpeptidases involved in cell-wall biosynthesis. Bacteria produce MBLs … Read more

Copper supplementation restores cytochrome c oxidase assembly defect in amitochondrial disease model of COA6 deficiency

In general, mitochondrial myopathies are neuromuscular disorders caused by dysfunctional mitochondria. When mitochondria function incorrectly, ATP is not produced, and the cell suffers. With enough cells suffering, an organism can have widespread problems, resulting in systemic failures. Unfortunately, mitochondrial diseases are very promiscuous, and individual mutations in many different proteins can cause each classified disease. … Read more

The Role of Transition Metal Transporters for Iron, Zinc, Manganese, and Copper in the Pathogenesis of Yersinia pestis

The plague is caused by the bacteria Yersinia pestis.  Infected rats carry the disease and pass it to fleas, the disease vector.  The bacteria grow in the fleas’ abdomen and are passed to humans through a flea bite.  There are three types of the plague; bubonic, septicemic and pneumonic.  The bubonic plague has an early … Read more

Loss of HIF2α in the Lung Alveolar Epithelium of Mice Leads to Enhanced Eosinophilic Inflammation in Cobalt-Induced Lung Injury

Hard metal lung disease (HMLD) is a rare illness caused by chronic exposure to cobalt and tungsten carbide. HMLD is most commonly developed by people who work in industries that use heavy metal tools that are ground down, heated, or both, releasing heavy metal particles into the air which can be inhaled. Cobalt is a … Read more

Heme Oxygenase-1 Protects Astroglia Against Manganese-Induced Oxidative Injury By Regulating Mitochondrial Quality Control

Manganism is a disease that arises as a direct result of long term exposure to high levels of Manganese. It is characterized by deposition of Manganese in the brain, and results in mitochondrial dysfunction. The most common treatment is removal from the area with high Manganese exposure, but this doesn’t work for everyone. Luckily, it’s … Read more

Zinc deficiency causes neural tube defects through attenuation of p53 ubiquitylation

Neural tube defects (NTDs) are the second most common birth defect worldwide and can occur do to environmental factors like micronutrition. Deficiencies in folic acid concentrations have been heavily associated with human NTDs due to neurulation’s dependency on the methionine cycle and folate cycle. Neurulation is the formation of the nervous system from the ectoderm … Read more