Abstract
In Chap. 3 we have shown some examples of how lipid-protein interactions lead to laterally segregated structures in membranes, and how the activity of proteins is related to physical properties of the phospholipids. In this chapter we will first discuss the relationship between membrane structure and bioenergetics, emphasizing that lipids may be part of the machinery involved in proton transport between protein components of the respiratory chain. Second we will present selected examples that relate membrane protein activity with specific phospholipids and we will discuss how this can be rationalized theoretically by introducing the concept of a lateral pressure profile of the membrane. Since the magnitude of lateral pressure within the membrane cannot be experimentally measured, we will show how using atomic force microscopy in force mode and single-molecule force spectroscopy, we can extract nanomechanical properties of the membranes related to protein packing. These properties, in particular the unfolding force or the force required to extract a membrane protein from a bilayer, are related to both the lateral pressure of pure lipid monolayers and the intrinsic surface curvature of monolayers. Finally, we will discuss the application of FRET to identify the phospholipid species present at the lipid-protein interface.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Notes
- 1.
The Faraday constant is equal to the product of the Avogadro constant and the proton charge: F = N A e = 96485.309 C mol−1.
- 2.
Concentration, ideally in molal scale, will be used by assuming that the activity coefficients of H+ and ions in general are nearly the same at both sides of the membrane.
- 3.
Δr G′ is the “transformed” Gibbs energy change, and it refers to the value of the magnitude at a given T, P, pH and ionic strength (I).
References
Attard GS, Templer RH, Smith WS, Hunt AN, Jackowski S. Modulation of CTP:phosphocholine cytidylyltransferase by membrane curvature elastic stress. Proc Natl Acad Sci U. S. A. 2000;97(16):9032–6.
Bogdanov M, Heacock P, Guan Z, Dowhan W. Plasticity of lipid-protein interactions in the function and topogenesis of the membrane protein lactose permease from Escherichia coli. Proc Natl Acad Sci U. S. A. 2010;107(34):15057–62.
Cantor RS. Lateral pressures in cell membranes: a mechanism for modulation of protein function. J Phys Chem. 1997;101(96):1723–5.
Cantor RS. The influence of membrane lateral pressures on simple geometric models of protein conformational equilibria. Chem Phys Lipids. 1999;101(1):45–56.
Caplan SR, Essig A. Bioenergetics and linear nonequilibrium thermodynamics the steady state. 2nd ed. NY: Harvard University Press; 1983.
Dowhan W, Mileykovskaya E, Bogdanov M. Diversity and versatility of lipid-protein interactions revealed by molecular genetic approaches. Biochim Biophys Acta. 2004;1666(1–2):19–39.
Elmore DE, Dougherty DA. Investigating lipid composition effects on the mechanosensitive channel of large conductance (MscL) using molecular dynamics simulations. Biophys J. 2003;85(3):1512–24.
Goormaghtigh E, Raussens V, Ruysschaert J-M. Attenuated total reflection infrared spectroscopy of proteins and lipids in biological membranes. Biochim Biophys Acta Rev Biomembr. 1999;1422:105–85.
Gullingsrud J, Schulten K. Lipid bilayer pressure profiles and mechanosensitive channel gating. Biophys J. 2004;86(6):3496–509.
Haines TH, Dencher NA. Cardiolipin: a proton trap for oxidative phosphorylation. FEBS Lett. 2002;528:35–9.
Houslay MD, Stanley KK. Dynamics of biological membranes. Chischester: Wiley; 1982.
Jiang Y, Lee A, Chen J, Ruta V, Cadene M, Chait BT, et al. X-ray structure of a voltage-dependent K+ channel. Nature. 2003;423(6935):33–41.
le Coutre J, Narasimhan LR, Patel CK, Kaback HR. The lipid bilayer determines helical tilt angle and function in lactose permease of Escherichia coli. Proc Natl Acad Sci U. S. A. 1997;94(19):10167–71.
le Coutre J, Kaback HR, Patel CK, Heginbotham L, Miller C. Fourier transform infrared spectroscopy reveals a rigid alpha-helical assembly for the tetrameric Streptomyces lividans K+ channel. Proc Natl Acad Sci U. S. A. 1998;95(11):6114–7.
Madden TD, Quinn PJ. Arrhenius discontinuities of Ca2+-ATPase activity are unrelated to changes in membrane lipid fluidity of sarcoplasmic reticulum. FEBS letters. 1979;197(1):110–2.
Marius P, Alvis SJ, East JM, Lee AG. The interfacial lipid binding site on the potassium channel KcsA is specific for anionic phospholipids. Biophys J. 2005;89(6):4081–9.
Merino-Montero S. Dissertation Thesis, University of Barcelona. 2005.
Mitchell P. Coupling of phosphorylation to electron and hydrogen transfer by a chemi-osmotic type of mechanism. Nature. 1961;191:144–8.
Muller DJ. AFM: a nanotool in membrane biology. Biochemistry. 2008;47(31):7986–98.
Ollila S. Lateral Pressure in Lipid Membranes and Its Role in Function of Membrane Proteins. Dissertation thesis. Tampere University of Technology. 2010.
Perozo E, Rees DC. Structure and mechanism in prokaryotic mechanosensitive channels. Curr. Opp. Struct. Biol. 2003;13:432–42.
Phillips R, Ursell T, Wiggins P, Sens P. Emerging roles for lipids in shaping membrane-protein function. Nature. 2009;459(7245):379–85.
Picas L, Montero MT, Morros A, Vázquez-Ibar JL, Hernández-Borrell J. Evidence of phosphatidylethanolamine and phosphatidylglycerol presence at the annular region of lactose permease of Escherichia coli. Biochim Biophys Acta Biomembr. 2010;1798(2):291–6.
Prats M, Tocanne JF, Teissié J. Lateral proton conduction along a lipid-water interface layer: a molecular mechanism for the role of hydration water molecules. Biochimie. 1989;71(1):33–6.
Putman M, van Veen HW, Konings WN. Molecular properties of bacterial multidrug transporters. Microbiol Mol Biol Rev. 2000;64(4):672–93.
Samuli Ollila OH, Róg T, Karttunen M, Vattulainen I. Role of sterol type on lateral pressure profiles of lipid membranes affecting membrane protein functionality: comparison between cholesterol, desmosterol, 7-dehydrocholesterol and ketosterol. J Struct Biol. 2007;159 2 SPEC. ISS. :311–23.
Schmidt D, Jiang Q-X, MacKinnon R. Phospholipids and the origin of cationic gating charges in voltage sensors. Nature. 2006;444(7120):775–9.
Seeger HM, Bortolotti CA, Alessandrini A, Facci P. Phase-transition-induced protein redistribution in lipid bilayers. J Phys Chem B. 2009;113(52):16654–9.
Serdiuk T, Madej MG, Sugihara J, Kawamura S, Mari SA, Kaback HR, et al. Substrate-induced changes in the structural properties of LacY. Proc Natl Acad Sci. 2014;111:E1571–80.
Serdiuk T, Sugihara J, Mari SA, Kaback HR, Müller DJ. Observing a lipid-dependent alteration in single lactose permeases. Structure. 2015;23(4):754–61.
Suárez-Germà C, Domènech Ò, Montero MT, Hernández-Borrell J. Effect of lactose permease presence on the structure and nanomechanics of two-component supported lipid bilayers. Biochim Biophys Acta Biomembr. 2014;1838(3):842–52.
Templer RH, Castle SJ, Curran a R, Rumbles G, Klug DR. Sensing isothermal changes in the lateral pressure in model membranes using di-pyrenyl phosphatidylcholine. Faraday Discuss. 1998;111:41–53; discussion 69–78.
Valiyaveetil FI, Zhou Y, MacKinnon R. Lipids in the structure, folding, and function of the KcsA K+ channel. Biochemistry. 2002;41(35):10771–7.
Vitrac H, Bogdanov M, Dowhan W. Proper fatty acid composition rather than an ionizable lipid amine is required for full transport function of lactose permease from Escherichia coli. J Biol Chem. 2013;288:5873–85.
Weingarth M, Prokofyev A, van der Cruijsen EAW, Nand D, Bonvin AMJJ, Pongs O, et al. Structural determinants aspects of specific lipid binding to potassium channels. J Am Chem Soc. 2013;135:3983–8.
Zhang W, Kaback HR. Effect of the lipid phase transition on the lactose permease from Escherichia coli. Biochemistry. 2000;39(49):14538–42.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
Copyright information
© 2016 The Author(s)
About this chapter
Cite this chapter
Borrell, J.H., Domènech, Ò., Keough, K.M.W. (2016). Dependence of Protein Membrane Mechanisms on Specific Physicochemical Lipid Properties. In: Membrane Protein – Lipid Interactions: Physics and Chemistry in the Bilayer. SpringerBriefs in Biochemistry and Molecular Biology. Springer, Cham. https://doi.org/10.1007/978-3-319-30277-5_4
Download citation
DOI: https://doi.org/10.1007/978-3-319-30277-5_4
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-30275-1
Online ISBN: 978-3-319-30277-5
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)