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Biochim Biophys Acta Gen Subj. 2020 Jan;1864(1):129434. doi: 10.1016/j.bbagen.2019.129434. Epub 2019 Sep 13.

Unfolding and partial refolding of a cellulase from the SDS-denatured state: From β-sheet to α-helix and back.

Author information

1
iNANO, Aarhus University, Gustav Wieds Vej 14, DK - 8000 Aarhus C, Denmark; Department of Chemistry, Aarhus University, Langelandsgade 140, DK - 8000 Aarhus C, Denmark.
2
Department of Molecular Biology and Genetics, Aarhus University, Gustav Wieds Vej 10C, DK - 8000 Aarhus C, Denmark.
3
iNANO, Aarhus University, Gustav Wieds Vej 14, DK - 8000 Aarhus C, Denmark; Department of Molecular Biology and Genetics, Aarhus University, Gustav Wieds Vej 10C, DK - 8000 Aarhus C, Denmark. Electronic address: dao@inano.au.dk.
4
iNANO, Aarhus University, Gustav Wieds Vej 14, DK - 8000 Aarhus C, Denmark; Department of Chemistry, Aarhus University, Langelandsgade 140, DK - 8000 Aarhus C, Denmark. Electronic address: jsp@chem.au.dk.

Abstract

Globular proteins are typically unfolded by SDS to form protein-decorated micelle-like structures. Several proteins have been shown subsequently to refold by addition of the nonionic surfactant octaethylene glycol monododecyl ether (C12E8). Thus SDS converts β-lactoglobulin, which has mainly β-sheet secondary structure, into a state rich in α-helicality, while addition of C12E8 leads to refolding and recovery of the original β-sheet structure. Here we extend these studies to the large β-sheet-rich cellulase Cel7b from Humicola insolens whose enzymatic activity provides a very sensitive refolding parameter. The enzymes widespread usage in the detergent industry makes it an obvious model system for protein-surfactant interactions. SDS-unfolding and subsequent refolding using C12E8 were investigated at pH 4.2 using near- and far-UV circular dichroism (CD), small-angle X-ray scattering (SAXS), isothermal titration calorimetry (ITC), size-exclusion chromatography (SEC) and activity measurements. The Cel7b:SDS complex can be described as a random configuration of 3-4 connected core-shell structures in which the protein is converted to a mainly α-helical secondary structure. Addition of C12E8 recovers almost all the secondary structure, part of the tertiary structure, about 50% of the activity and dissociates part of the protein population completely from detergent micelles. The lack of complete refolding may be due to charge neutralisation of Cel7b by SDS, kinetically trapping the enzyme into aggregated structures. In support of this, aggregates did not form when C12E8 was first mixed with Cel7b followed by addition of SDS. Formation of such aggregates may be a general phenomenon hampering quantitative refolding from the SDS-denatured state.

KEYWORDS:

Cellulase; Charge neutralisation; Refolding; SAXS; Surfactant; Unfolding

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