Literature DB >> 31994240

An in vitro mimic of in-cell solvation for protein folding studies.

Caitlin M Davis1,2, Jonathan Deutsch3, Martin Gruebele1,2,3.   

Abstract

Ficoll, an inert macromolecule, is a common in vitro crowder, but by itself it does not reproduce in-cell stability or kinetic trends for protein folding. Lysis buffer, which contains ions, glycerol as a simple kosmotrope, and mimics small crowders with hydrophilic/hydrophobic patches, can reproduce sticking trends observed in cells but not the crowding. We previously suggested that the proper combination of Ficoll and lysis buffer could reproduce the opposite in-cell folding stability trend of two proteins: variable major protein-like sequence expressed (VlsE) is destabilized in eukaryotic cells and phosphoglycerate kinase (PGK) is stabilized. Here, to discover a well-characterized solvation environment that mimics in-cell stabilities for these two very differently behaved proteins, we conduct a two-dimensional scan of Ficoll (0-250 mg/ml) and lysis buffer (0-75%) mixtures. Contrary to our previous expectation, we show that mixtures of Ficoll and lysis buffer have a significant nonadditive effect on the folding stability. Lysis buffer enhances the stabilizing effect of Ficoll on PGK and inhibits the stabilizing effect of Ficoll on VlsE. We demonstrate that a combination of 150 mg/ml Ficoll and 60% lysis buffer can be used as an in vitro mimic to account for both crowding and non-steric effects on PGK and VlsE stability and folding kinetics in the cell. Our results also suggest that this mixture is close to the point where phase separation will occur. The simple mixture proposed here, based on commercially available reagents, could be a useful tool to study a variety of cytoplasmic protein interactions, such as folding, binding and assembly, and enzymatic reactions. SIGNIFICANCE STATEMENT: The complexity of the in-cell environment is difficult to reproduce in the test tube. Here we validate a mimic of cellular crowding and sticking interactions in a test tube using two proteins that are differently impacted by the cell: one is stabilized and the other is destabilized. This mimic is a starting point to reproduce cellular effects on a variety of protein and biomolecular interactions, such as folding and binding.
© 2020 The Protein Society.

Entities:  

Keywords:  fluorescence resonance energy transfer (FRET); laser-induced temperature jump; macromolecular crowding; phosphoglycerate kinase (PGK); protein folding; quinary interactions; thermal denaturation; variable major protein-like sequence expressed (VlsE)

Mesh:

Substances:

Year:  2020        PMID: 31994240      PMCID: PMC7096716          DOI: 10.1002/pro.3833

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


  37 in total

1.  Life in a crowded world.

Authors:  Germán Rivas; Frank Ferrone; Judith Herzfeld
Journal:  EMBO Rep       Date:  2004-01       Impact factor: 8.807

2.  The diffusion coefficient for PGK folding in eukaryotic cells.

Authors:  Apratim Dhar; Simon Ebbinghaus; Zhen Shen; Tripta Mishra; Martin Gruebele
Journal:  Biophys J       Date:  2010-11-03       Impact factor: 4.033

3.  Thermodynamics of protein destabilization in live cells.

Authors:  Jens Danielsson; Xin Mu; Lisa Lang; Huabing Wang; Andres Binolfi; François-Xavier Theillet; Beata Bekei; Derek T Logan; Philipp Selenko; Håkan Wennerström; Mikael Oliveberg
Journal:  Proc Natl Acad Sci U S A       Date:  2015-09-21       Impact factor: 11.205

4.  Ribosome Mediated Quinary Interactions Modulate In-Cell Protein Activities.

Authors:  Christopher M DeMott; Subhabrata Majumder; David S Burz; Sergey Reverdatto; Alexander Shekhtman
Journal:  Biochemistry       Date:  2017-08-03       Impact factor: 3.162

Review 5.  Macromolecular crowding and confinement: biochemical, biophysical, and potential physiological consequences.

Authors:  Huan-Xiang Zhou; Germán Rivas; Allen P Minton
Journal:  Annu Rev Biophys       Date:  2008       Impact factor: 12.981

6.  Protein folding stability and dynamics imaged in a living cell.

Authors:  Simon Ebbinghaus; Apratim Dhar; J Douglas McDonald; Martin Gruebele
Journal:  Nat Methods       Date:  2010-02-28       Impact factor: 28.547

7.  Physicochemical code for quinary protein interactions in Escherichia coli.

Authors:  Xin Mu; Seongil Choi; Lisa Lang; David Mowray; Nikolay V Dokholyan; Jens Danielsson; Mikael Oliveberg
Journal:  Proc Natl Acad Sci U S A       Date:  2017-05-23       Impact factor: 11.205

8.  Subcellular modulation of protein VlsE stability and folding kinetics.

Authors:  Jonathan Tai; Kapil Dave; Vincent Hahn; Irisbel Guzman; Martin Gruebele
Journal:  FEBS Lett       Date:  2016-05-17       Impact factor: 4.124

9.  Probing protein quinary interactions by in-cell nuclear magnetic resonance spectroscopy.

Authors:  Subhabrata Majumder; Jing Xue; Christopher M DeMott; Sergey Reverdatto; David S Burz; Alexander Shekhtman
Journal:  Biochemistry       Date:  2015-04-27       Impact factor: 3.162

10.  Behavior of Plasmodium falciparum purine nucleoside phosphorylase in macromolecular crowded environment.

Authors:  Manish Kumar Suthar; Pawan Kumar Doharey; Anita Verma; Jitendra Kumar Saxena
Journal:  Int J Biol Macromol       Date:  2013-10-01       Impact factor: 6.953

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  2 in total

1.  An in vitro mimic of in-cell solvation for protein folding studies.

Authors:  Caitlin M Davis; Jonathan Deutsch; Martin Gruebele
Journal:  Protein Sci       Date:  2020-02-06       Impact factor: 6.725

2.  Investigating molecular crowding during cell division and hyperosmotic stress in budding yeast with FRET.

Authors:  Sarah Lecinski; Jack W Shepherd; Lewis Frame; Imogen Hayton; Chris MacDonald; Mark C Leake
Journal:  Curr Top Membr       Date:  2021-11-16       Impact factor: 3.049

  2 in total

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