Multiple conformational states of a new hematopoietic cytokine (megakaryocyte growth and development factor): pH- and urea-induced denaturation

• Published in: Proteins, structure, function, and bioinformatics structure, function, and bioinformatics, 1998-09, Vol.32 (4), p.495-503
• Main Authors: Hamburger, James B., Chen, Eileen, Narhi, Linda O., Wu, Gay-May, Brems, David N.
• Format: Article
• Language: English
• Subjects: Circular Dichroism; conformation; cytokine; Cytokines - chemistry; equilibrium denaturation; Humans; Hydrogen-Ion Concentration; megakaryocyte growth and development factor; Protein Conformation; Protein Denaturation; Protein Folding; Recombinant Proteins - chemistry; thrombopoietin; Thrombopoietin - chemistry; Ultraviolet Rays; Urea
• ISSN: 0887-3585; 1097-0134
• DOI: 10.1002/(SICI)1097-0134(19980901)32:4<495::AID-PROT7>3.0.CO;2-F

The effect of pH and urea on the conformation of recombinant human megakaryocyte growth and development factor (rHuMGDF) was determined by circular dichroism, intrinsic fluorescence spectroscopy, and equilibrium ultracentrifugation. The conformation of rHuMGDF was dependent on pH and urea concentration. Multiple folding forms were evidenced by multiple pH‐induced transitions and urea‐induced equilibrium transitions that deviated from a simple two‐state process. In neutral to alkaline pH, rHuMGDF exists as a monomer, but an acid‐induced conformational state self‐associates to form a soluble aggregate. A folding intermediate(s) was observed with a more stable secondary structure than tertiary structure and was dependent on the pH of the urea‐induced denaturation. The differences in the stabilities of the folding states were most distinct in the pH range of 4.5 to 6.5. The presence of intermediates in the folding pathway of rHuMGDF are similar to findings of previous studies of related growth factors that share a common three‐dimensional structure. Proteins 32:495–503, 1998. © 1998 Wiley‐Liss, Inc.