Literature DB >> 25323391

Computational study of elements of stability of a four-helix bundle protein biosurfactant.

Andrea Schaller1, Natalie K Connors, Mirjana Dimitrijev Dwyer, Stefan A Oelmeier, Jürgen Hubbuch, Anton P J Middelberg.   

Abstract

Biosurfactants are surface-active molecules produced principally by microorganisms. They are a sustainable alternative to chemically-synthesized surfactants, having the advantages of being non-toxic, highly functional, eco-friendly and biodegradable. However they are currently only used in a few industrial products due to costs associated with production and purification, which exceed those for commodity chemical surfactants. DAMP4, a member of a four-helix bundle biosurfactant protein family, can be produced in soluble form and at high yield in Escherichia coli, and can be recovered using a facile thermal phase-separation approach. As such, it encompasses an interesting synergy of biomolecular and chemical engineering with prospects for low-cost production even for industrial sectors. DAMP4 is highly functional, and due to its extraordinary thermal stability it can be purified in a simple two-step process, in which the combination of high temperature and salt leads to denaturation of all contaminants, whereas DAMP4 stays stable in solution and can be recovered by filtration. This study aimed to characterize and understand the fundamental drivers of DAMP4 stability to guide further process and surfactant design studies. The complementary use of experiments and molecular dynamics simulation revealed a broad pH and temperature tolerance for DAMP4, with a melting point of 122.4 °C, suggesting the hydrophobic core as the major contributor to thermal stability. Simulation of systematically created in silico variants of DAMP4 showed an influence of number and location of hydrophilic mutations in the hydrophobic core on stability, demonstrating a tolerance of up to three mutations before a strong loss in stability occurred. The results suggest a consideration of a balance of stability, functionality and kinetics for new designs according to their application, aiming for maximal functionality but at adequate stability to allow for cost-efficient production using thermal phase separation approaches.

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Year:  2014        PMID: 25323391     DOI: 10.1007/s10822-014-9803-6

Source DB:  PubMed          Journal:  J Comput Aided Mol Des        ISSN: 0920-654X            Impact factor:   3.686


  45 in total

1.  Increasing the precision of comparative models with YASARA NOVA--a self-parameterizing force field.

Authors:  Elmar Krieger; Günther Koraimann; Gert Vriend
Journal:  Proteins       Date:  2002-05-15

2.  Stably folded de novo proteins from a designed combinatorial library.

Authors:  Yinan Wei; Tun Liu; Stephen L Sazinsky; David A Moffet; István Pelczer; Michael H Hecht
Journal:  Protein Sci       Date:  2003-01       Impact factor: 6.725

3.  Increasing temperature accelerates protein unfolding without changing the pathway of unfolding.

Authors:  Ryan Day; Brian J Bennion; Sihyun Ham; Valerie Daggett
Journal:  J Mol Biol       Date:  2002-09-06       Impact factor: 5.469

4.  A point-charge force field for molecular mechanics simulations of proteins based on condensed-phase quantum mechanical calculations.

Authors:  Yong Duan; Chun Wu; Shibasish Chowdhury; Mathew C Lee; Guoming Xiong; Wei Zhang; Rong Yang; Piotr Cieplak; Ray Luo; Taisung Lee; James Caldwell; Junmei Wang; Peter Kollman
Journal:  J Comput Chem       Date:  2003-12       Impact factor: 3.376

5.  Making optimal use of empirical energy functions: force-field parameterization in crystal space.

Authors:  Elmar Krieger; Tom Darden; Sander B Nabuurs; Alexei Finkelstein; Gert Vriend
Journal:  Proteins       Date:  2004-12-01

6.  Redesigning the hydrophobic core of a four-helix-bundle protein.

Authors:  M Munson; R O'Brien; J M Sturtevant; L Regan
Journal:  Protein Sci       Date:  1994-11       Impact factor: 6.725

7.  Insights into the role of protein molecule size and structure on interfacial properties using designed sequences.

Authors:  Mirjana Dimitrijev Dwyer; Lizhong He; Michael James; Andrew Nelson; Anton P J Middelberg
Journal:  J R Soc Interface       Date:  2013-01-09       Impact factor: 4.118

Review 8.  Microbial biosurfactants: challenges and opportunities for future exploitation.

Authors:  Roger Marchant; Ibrahim M Banat
Journal:  Trends Biotechnol       Date:  2012-08-16       Impact factor: 19.536

Review 9.  Protein arginine methylation in mammals: who, what, and why.

Authors:  Mark T Bedford; Steven G Clarke
Journal:  Mol Cell       Date:  2009-01-16       Impact factor: 17.970

10.  Hydrogen bonding motifs of protein side chains: descriptions of binding of arginine and amide groups.

Authors:  L Shimoni; J P Glusker
Journal:  Protein Sci       Date:  1995-01       Impact factor: 6.725

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