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Fusion Protein Nomenclature

A fusion protein is defined as a multifunctional protein derived from a single nucleotide sequence that may contain 2 or more genes or portions of genes with or without amino acid linker sequences. The genes should originally code for separate proteins, both w

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A fusion protein is defined as a multifunctional protein derived from a single nucleotide sequence that may contain 2 or more genes or portions of genes with or without amino acid linker sequences. The genes should originally code for separate proteins, both with pharmacological action (e.g., action and targeting). The suffix “- fusp ” for “fusion protein” will be used with a syllable formed from 1 consonant and 1 vowel added before the suffix to indicate: (a) the pharmaceutical action (consonant); and (b) the target (vowel). The meanings of these infix letters are given below. The “- fusp ” naming scheme is not designed to give comprehensive information about the substance, but to indicate it is a fusion protein and to indicate its action and target. The description on the USAN adoption statement will provide more extensive information about the precise content and action of the fusion protein. Bifunctional fusion proteins with 1 component being a peptide will only be included in the “ –fusp ” naming scheme if it has a clear pharmacological action or targeting role. If the role of the peptide is not clear or is vague, other naming conventions should be used. All components must be endowed with a pharmacological activity. In a bifunctional fusion protein, if 1 component has a purely stabilizing function (e.g., to increase half-life), no “ -fusp ” will be assigned. For instance, if the component is a stabilizing Fc fragment, the “ ef- ” prefix should be used, not “ -fusp ”. In a multifunctional fusion protein that has more than 1 pharmacological action, but also contains a stabilizing Fc fragment, both “ ef- ” and “ -fusp ” should be used. If both components of the fusion protein have a targeting action, and 1 of them is derived from a monoclonal antibody (mAb) or from a mAb fragment, when assigning the identifying infix letters, the “ -a- ” for antibody takes priority. For instance, the fusion of a receptor with an antibody will be “ -ra- ” (where r stands for receptor and a for antibody ) not “ -be- ” (where b stands for binding protein and e for receptor ). The infix letters will not distinguish between mAb or mAb fragments; in all these cases the letter “ a ” will be selected. Multiple mAb or mAb fragments will be named using the “ -mab ” nomenclature scheme, not the “ -fusp ” scheme. If more than 2 components are present, the 2 infix letters will still be used to represent the different action/targeting by class: e.g., if a fusion protein is composed by 2 mAbs and 1 receptor, the USAN will end in “- rafusp .”

Infix Letters and Their Meaning

These letters have the following “action” meanings associated with them:

  • b = Binding protein
  • c = Encapsulation protein
  • d =
  • f = Hormone
  • g = Antigen
  • k = Cytokine
  • l =
  • m = Membrane protein
  • n = Enzyme
  • p = Apoptosis
  • r = Receptor
  • s =
  • t = T-cell receptor
  • v = Multiple actions/proteins
  • x = Toxin
  • z =

These letters have the following “targeting” meanings associated with them:

  • a = Antibody
  • e = Receptor
  • i = Antigen
  • o = Other
  • u = Untargeted

Please be aware of the additional notes:

  • v = will be used when a multifunctional fusion protein has multiple and not related actions;
  • o = will be used when some other targeting mechanism (i.e., not antibody, receptor or antigen) is used in a bifunctional fusion protein or in a multifunctional fusion protein with multiple unrelated targeting;
  • u = will be used when a fusion protein has multiple actions and no targeting;
  • h, j, q, w, y = these consonants were excluded to facilitate translation.

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Related questions

01How does interleukin-2 (IL-2)-diphtheria toxin fusion protein work?

Interleukin-2 (IL-2)-diphtheria toxin fusion protein is a biological product used for the treatment of cutaneous T-cell lymphoma (CTCL) in adults. IL-2-diphtheria toxin fusion protein is a kind of treatment that is designed to kill cancer cells in cutaneous T-cell lymphoma by carrying and releasing the diphtheria toxin inside the tumor cells. Cutaneous T-cell lymphomas are a group of rare cancers that start in the T-lymphocytes, also known as T-cells, an integral part of the immune system. CTCL affects the skin, but it is not a skin cancer. It is a type of lymphoma in which T-cells within the skin become cancerous, cause inflammations and rashes, and damage the skin. The skin contains a large number of T-cells which help fight infections. CTCL occurs when these T-cells turn abnormal and grow out of control. Initially it only affects the skin, but can spread to other organs such as lymph nodes, liver and spleen, in advanced stages. CTCL is classified as a type of non-Hodgkin lymphoma (NHL). Interleukin-2 is a protein produced by activated T-cells, and is a growth factor that promotes the growth of T-cells. The activated T-cells in the skin in cutaneous T-cell lymphomas produce this protein which aids the cancerous growth of T-cells. Interleukin-2 (IL-2)-diphtheria toxin fusion protein binds to IL-2 receptors on the tumor cells and kills them. Interleukin-2 (IL-2)-diphtheria toxin fusion protein is produced using DNA recombinant technology and contains human IL-2 and diphtheria toxin fragments. The IL-2 helps the drug bind to T-cells that express IL-2 receptors, and once the molecule enters the cell, the diphtheria toxin separates and inhibits protein synthesis, which leads to cell death. Currently, the only approved interleukin-2 (IL-2)-diphtheria toxin fusion protein therapy is denileukin diftitiox. It was originally approved by the FDA to treat CTCL, under the brand name of Ontak in 1999. Ontak was withdrawn in 2014, and the treatment has now been approved in August 2024 under the brand name of Lymphir.

Source: www.rxlist.com ↗
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