Methemalbumin: reality and myth

J W George1

  • 1The California Primate Research Center University of California, Davis, Davis, California 95616.

Insights

Methemalbumin formation, often cited as a universal albumin trait, is actually limited to a few species. This review clarifies true methemalbumin characteristics and debunks its presence in domestic animals.

Area of Science:

  • Biochemistry
  • Veterinary Medicine
  • Comparative Physiology

Background:

  • Albumin's capacity to bind oxidized heme, forming methemalbumin, is widely assumed across animal species.
  • This assumption has led to the misconception of methemalbumin presence in domestic animals.
  • Interspecies variations in albumin's heme-binding properties are often overlooked.

Purpose of the Study:

  • To review the scientific literature on methemalbumin formation.
  • To define the chemical characteristics of true methemalbumin.
  • To address and correct the myth of methemalbumin in domestic animals.

Main Methods:

  • Comprehensive literature search on methemalbumin and albumin-heme interactions.
  • Analysis of chemical properties defining methemalbumin.
  • Comparative review of albumin function across different animal species.

Main Results:

  • Methemalbumin formation is not a universal characteristic of albumin.
  • Only albumin from a limited number of species exhibits the ability to form methemalbumin.
  • The literature contains instances of 'mythical' methemalbumin due to misidentification or misinterpretation.

Conclusions:

  • The widespread belief in methemalbumin in domestic animals is a myth.
  • Accurate identification of methemalbumin requires understanding species-specific albumin characteristics.
  • Further research may clarify the precise biochemical differences in albumin across species regarding heme binding.

Related Concept Videos

Proteomics01:33

Proteomics

A proteome is the entire set of proteins that a cell type produces. We can study proteomes using the knowledge of genomes because genes code for mRNAs, and the mRNAs encode proteins. Although mRNA analysis is a step in the right direction, not all mRNAs are translated into proteins.
Proteomics is the study of proteomes' function. It involves the large-scale systematic study of the proteome to denote the protein complement expressed by a genome. Scientist Mark Wilkins coined the term proteomics...
Overview of Protein Metabolism01:21

Overview of Protein Metabolism

Proteins are broken down into amino acids during digestion. Unlike fats and carbohydrates, which are stored for later use, proteins are not. Instead, amino acids are either used to produce ATP through oxidation or contribute to the creation of new proteins for the growth and repair of the body. Any surplus amino acids from the diet are converted into glucose or triglycerides rather than excreted.
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...
Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
Phase II Reactions: Methylation Reactions01:17

Phase II Reactions: Methylation Reactions

Methylation is a phase II biotransformation process involving the attachment of a methyl group to a substrate. Enzymes known as methyltransferases orchestrate this reaction.
The mechanism of methylation unfolds in two stages. The first stage sees a methyltransferase enzyme facilitating the transfer of a methyl group from S-adenosylmethionine (SAM) to the substrate, forming S-adenosylhomocysteine (SAH). The second stage involves further metabolism of SAH into homocysteine, which can be recycled...
Hepatic Encephalopathy01:29

Hepatic Encephalopathy

DefinitionHepatic encephalopathy is a reversible neurologic syndrome that results from advanced liver dysfunction or portosystemic shunting. It leads to disturbances in cognition, behavior, and motor function due to the brain’s exposure to gut-derived toxins that the liver fails to detoxify.EtiologyThis condition develops either in the setting of acute fulminant hepatitis or progressively during chronic liver disease, such as cirrhosis and portal hypertension. Portosystemic shunting—including...