The tenth fibronectin type III domain (human, PDB 1TTG)
Variable domain of an antibody's lambda light chain (human, PDB 2RHE)

Monobodies, also known as adnectins, are genetically engineered proteins that are able to bind to antigens. Despite their name, they are not structurally related to antibodies, which makes them a type of antibody mimetic. They are being developed by Adnexus, a biotechnology company which has been part of Bristol-Myers Squibb since 2007. The monobody angiocept (CT-322), a VEGF receptor antagonist, has entered Phase II clinical trials investigating the treatment of glioblastoma in October 2007.[1][2] It is also being studied for the treatment of other types of cancer, such as non-small cell lung cancer[3] and colorectal cancer[4].


Monobodies consist of 94 amino acids and have a molecular mass of about 10 kDa, fifteen times smaller than an IgG type antibody and comparable to the size of a single variable domain of an antibody. They are based on the structure of human fibronectin, more specifically on its tenth extracellular type III domain. This domain has a structure similar to antibody variable domains, with seven beta sheets forming a barrel and three exposed loops on each side corresponding to the three complementarity determining regions.[5] Monobodies lack binding sites for metal ions and the central disulfide bond.

Monobodies with specificity for different proteins can be tailored by modifying the loops BC (between the second and third beta sheets) and FG (between the sixth and seventh sheets).[6]

See also


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