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Updated: Aug 11, 2026

Determination of the Relative Potency of an Anti-TNF Monoclonal Antibody (mAb) by Neutralizing TNF Using an In Vitro Bioanalytical Method
Published on: September 16, 2017
Tumour necrosis factor is in equilibrium with a trimeric molten globule at low pH
1Department of Biochemistry and Genetics, Medical School, University of Newcastle upon Tyne, UK.
Abstract:
The reversible acid denaturation of tumour necrosis factor, TNF alpha, a trimeric, all-beta protein, leads to significant conformational changes within the molecule. A change in far UV CD spectra reveals a shift in the secondary structure content of the protein, with alpha-helical structure being induced. Loss of ellipticity in the near UV reflects a loss of tertiary interactions. This form of TNF is both compact and trimeric, as revealed by fluorescence anisotropy and sedimentation velocity analysis, respectively. Acid-denatured TNF therefore possesses the defining features of the molten globule intermediate while retaining the ability of the still incompletely folded monomers to exhibit the surface specificity necessary for maintaining the trimeric state.
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