Literature DB >> 34156613

Refolding of Hemoglobin Under Macromolecular Confinement: Impersonating In Vivo Volume Exclusion.

Gufran Ahmed Siddiqui1, Aabgeena Naeem2.   

Abstract

Biomacromolecules evolve and function inside the cell under crowded conditions. The effect of macromolecular crowding and confinement on nature and interactions of biomacromolecules cannot be ruled out. This study demonstrates the effect of volume exclusion due to macromolecular crowding on refolding rate of Gn-HCl induced unfolded hemoglobin. The in vivo like crowding milieu was created using dextran 70. Unfolding of Hb was followed by the absorbance at 280 nm and intrinsic fluorescence intensity along with a bathochromic shift that shows the destabilization of Hb in the presence of the denaturing agent. This was supported by a decrease in soret absorbance, increased hydrodynamic radii and loss in secondary structure, evidenced from dynamic light scattering and circular dichroism experiments respectively. Refolding process of Hb was followed by an increase in soret absorbance, decrease in intrinsic fluorescence intensity with a hypsochromic shift, decreased hydrodynamic radii and gain in secondary structural content. The results revealed that the effect of confinement and volume exclusion is insignificant on the process of Hb refolding.
© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Circular dichroism; Hemoglobin; Macromolecular crowding; Refolding; Tryptophan fluorescence; Volume exclusion

Mesh:

Substances:

Year:  2021        PMID: 34156613     DOI: 10.1007/s10895-021-02751-y

Source DB:  PubMed          Journal:  J Fluoresc        ISSN: 1053-0509            Impact factor:   2.217


  8 in total

1.  Effects of macromolecular crowding on the refolding of glucose- 6-phosphate dehydrogenase and protein disulfide isomerase.

Authors:  J Li; S Zhang; C Wang
Journal:  J Biol Chem       Date:  2001-07-09       Impact factor: 5.157

2.  Molecular crowding enhances native state stability and refolding rates of globular proteins.

Authors:  Margaret S Cheung; Dmitri Klimov; D Thirumalai
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-21       Impact factor: 11.205

3.  Macromolecular crowding increases structural content of folded proteins.

Authors:  Michael Perham; Loren Stagg; Pernilla Wittung-Stafshede
Journal:  FEBS Lett       Date:  2007-10-01       Impact factor: 4.124

4.  Effect of mixed macromolecular crowding agents on protein folding.

Authors:  Huan-Xiang Zhou
Journal:  Proteins       Date:  2008-09

5.  Efficacy of macromolecular crowding in forcing proteins to fold.

Authors:  Youxing Qu; D W Bolen
Journal:  Biophys Chem       Date:  2002-12-10       Impact factor: 2.352

6.  Aggregation of globular protein as a consequences of macromolecular crowding: A time and concentration dependent study.

Authors:  Gufran Ahmed Siddiqui; Aabgeena Naeem
Journal:  Int J Biol Macromol       Date:  2017-12-05       Impact factor: 6.953

7.  Mixed macromolecular crowding accelerates the oxidative refolding of reduced, denatured lysozyme: implications for protein folding in intracellular environments.

Authors:  Bing-Rui Zhou; Yi Liang; Fen Du; Zheng Zhou; Jie Chen
Journal:  J Biol Chem       Date:  2004-10-19       Impact factor: 5.157

8.  Effect of macromolecular crowding on protein folding dynamics at the secondary structure level.

Authors:  Smita Mukherjee; Matthias M Waegele; Pramit Chowdhury; Lin Guo; Feng Gai
Journal:  J Mol Biol       Date:  2009-08-13       Impact factor: 5.469

  8 in total

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