The Transport and Organization of Cholesterol in Planar Solid-Supported Lipid Bilayer Depend on the Phospholipid Flip-Flop Rate

Similar documents
Phase Transition Behaviours of the Supported DPPC Bilayer. Investigated by Sum Frequency Generation (SFG) and Atomic Force

Phosphatidylcholines are a class of glycerophospholipids which along with other phospholipids

Calcium-dependent Hydrolysis of Supported Planar Lipids Were Triggered by honey bee venom Phospholipase A 2 with Right Orientation at Interface

Methanol Perturbing Modeling Cell Membranes Investigated using Linear and Nonlinear Vibrational Spectroscopy

Journal of Structural Biology

MARTINI Coarse-Grained Model of Triton TX-100 in Pure DPPC. Monolayer and Bilayer Interfaces. Supporting Information

Effects of hydrocarbon chains saturation degree on molecular interaction between phospholipids and cholesterol in mixed monolayers

Chapter 1 Membrane Structure and Function

Model for measurement of water layer thickness under lipid bilayers by surface plasmon resonance

Neutron reflectivity in biology and medicine. Jayne Lawrence

Polarization and Circular Dichroism (Notes 17)

Physical Cell Biology Lecture 10: membranes elasticity and geometry. Hydrophobicity as an entropic effect

Structure and Phase Behaviour of Binary Mixtures of Cholesterol with DPPC and DMPC

Lipids and Membranes

MOLECULAR DYNAMICS SIMULATION OF MIXED LIPID BILAYER WITH DPPC AND MPPC: EFFECT OF CONFIGURATIONS IN GEL-PHASE

Methods and Materials

Na + and Ca 2+ Effect on the Hydration and Orientation of the Phosphate Group of DPPC at Air-Water and Air-Hydrated Silica Interfaces

AFM In Liquid: A High Sensitivity Study On Biological Membranes

Christopher W. Avery, Abhigyan Som, Yongjiang Xu, Gregory N. Tew, and Zhan Chen*,

Supplementary information for Effects of Stretching Speed on. Mechanical Rupture of Phospholipid/Cholesterol Bilayers: Molecular

Flip-Flop Induced Relaxation Of Bending Energy: Implications For Membrane Remodeling

Interfacial Behavior of Cholesterol, 7-Ketocholesterol and 5β,6β-Epoxycholesterol in. Phosphatidylcholine Monolayers DISSERTATION

Supplementary Materials for

Interactions of Polyethylenimines with Zwitterionic and. Anionic Lipid Membranes

Supplementary Information for. Intermolecular Headgroup Interaction and Hydration as Driving Forces for Lipid Transmembrane Asymmetry

Graphene Quantum Dots-Band-Aids Used for Wound Disinfection

Chemistry and Physics of Lipids 96 (1998) David D. Baldyga, Richard A. Dluhy * Received 24 May 1998; accepted 29 May 1998

Colloids and Surfaces B: Biointerfaces

Possible Molecular Mechanism to Account for Wavelength Dependence of Equilibration Rates of Patman and Laurdan in Phosphatidylcholine Bilayers

Electronic Supporting Information

Supporting material. Membrane permeation induced by aggregates of human islet amyloid polypeptides

INTERFACIAL VIBRATIONAL CHEMISTRY OF I. MIXED SURFACTANT SYSTEMS II. ALKYL HALIDE UPTAKE AND ATMOSPHERIC IMPLICATIONS. A Thesis

Chemical Surface Transformation 1

Development of Biomimetic Surfaces by Vesicle Fusion

PROCEEDINGS OF THE YEREVAN STATE UNIVERSITY

The Interaction between Lipid Bilayers and Biological Membranes. Chapter 18

A: All atom molecular simulation systems

Chapter 12: Membranes. Voet & Voet: Pages

P NMR in lipid membranes. CSA recoupling.

Membranes formed by bilayers of phospholipids play a

Effect of temperature on liposome structures studied using EPR spectroscopy

Supplement 2 - Quantifying sample mosaicity

Roles of Sterol Derivatives in Regulating the Properties of Phospholipid Bilayer Systems

induced inactivation of lung surfactants

Photochemical Applications to the Study of Complexity Phospholipid Bilayer Environments

Protein directed assembly of lipids

Polyoxometalate Macroion Induced Phase and Morphology

0.5 nm nm acyl tail region (hydrophobic) 1.5 nm. Hydrophobic repulsion organizes amphiphilic molecules: These scales are 5 10xk B T:

Supplementary Information: Liquid-liquid phase coexistence in lipid membranes observed by natural abundance 1 H 13 C solid-state NMR

STUDIES OF INTERACTIONS BETWEEN PEPTIDES/PROTEINS AND LIPID BILAYERS USING SUM FREQUENCY GENERATION VIBRATIONAL SPECTROSCOPY

Supporting Information

Lecture 15. Membrane Proteins I

Structure and dynamics of water and lipid molecules in charged anionic DMPG lipid bilayer membranes

Penetration of Gold Nanoparticle through Human Skin: Unraveling Its Mechanisms at the Molecular Scale

2

1,2-Diacyl-Phosphatidylcholine Flip-Flop Measured Directly by Sum-Frequency Vibrational Spectroscopy

H-NMR in liquid crystals and membranes

Electron-Transfer Properties of Cytochrome c Langmuir-Blodgett Films and Interactions of Cytochrome c with Lipids

Title. Author(s)Wu, Heng-Liang; Tong, Yujin; Peng, Qiling; Li, Na; Y. CitationPhysical chemistry chemical physics, 18(3):

Simulationen von Lipidmembranen

Chapter 12: Mass Spectrometry: molecular weight of the sample

Structure-Transport Relationship in Organized Soft Matter Systems by Diffusion NMR. Sergey Vasenkov

Electronic Supplementary Information

PRODUCT CATALOG. Phospholipids for Pharmaceutical Applications. We Invest in Quality.

Structure and properties of phospholipid peptide monolayers containing monomeric SP-B 1 25 II. Peptide conformation by infrared spectroscopy

Chapter 5 Stereochemistry

Chapter 9 - Biological Membranes. Membranes form a semi-permeable boundary between a cell and its environment.

Interfacial Water Structure Associated with Phospholipid Membranes Studied by Phase-Sensitive Vibrational Sum Frequency Generation Spectroscopy

Interactions between Fluoroquinolones and lipids: Biophysical studies

Lipids are macromolecules, but NOT polymers. They are amphipathic composed of a phosphate head and two fatty acid tails attached to a glycerol

Gen. Physiol. Biophys. (1988), 7,

Lipids fatty, oily, or waxy hydrophobic organic compounds.

Interactions between Bisphosphate. Geminis and Sodium Lauryl Ether

Molecular dynamics simulations of the interactions of medicinal plant extracts and drugs with lipid bilayer membranes

Week 5 Section. Junaid Malek, M.D.

Pressure Modulation of the Enzymatic Activity of. Phospholipase A2, a Putative Membraneassociated

Biology Chapter 2 Review

The main biological functions of the many varied types of lipids include: energy storage protection insulation regulation of physiological processes

Life Sciences 1a. Practice Problems 4

Doğangün et al. Supporting Information for. Hydrogen Bond Networks Near Supported Lipid Bilayers from Vibrational Sum

Lateral Pressure Dependence of the Phospholipid Transmembrane Diffusion Rate in Planar-Supported Lipid Bilayers

Coarse grained simulations of Lipid Bilayer Membranes

Supplementary Figures

Studying Orientation and Conformation of α-helical Peptides at Interfaces

Improving photovoltaic performance of solid-state ZnO/CdTe coreshell. nanorod array solar cells by a thin CdS interfacial layer

ORGANIZATION OF ANTIBIOTIC AMPHOTERICIN B IN MODEL LIPID MEMBRANES. A MINI REVIEW

Colloid chemistry. Lecture 10: Surfactants

Biological Membranes. Lipid Membranes. Bilayer Permeability. Common Features of Biological Membranes. A highly selective permeability barrier

Effects of Epicholesterol on the Phosphatidylcholine Bilayer: A Molecular Simulation Study

Inorganic compounds: Usually do not contain carbon H 2 O Ca 3 (PO 4 ) 2 NaCl Carbon containing molecules not considered organic: CO 2

Time-Resolved FT-IR Microspectroscopy of Protein Aggregation Induced by Heat-Shock in Live Cells

ESR and Monolayer Study of the Localization of Coenzyme Q 10 in Artificial Membranes

For questions 1-4, match the carbohydrate with its size/functional group name:

Supporting Information. Magnetic Field and Chirality Effects on Electrochemical Charge Transfer Rates: Spin. Dependent Electrochemistry

Second harmonic spectroscopy: detection and orientation of molecules at a biomembrane interface

Structure of Dipalmitoylphosphatidylcholine/Cholesterol Bilayer at Low and High Cholesterol Concentrations: Molecular Dynamics Simulation

Raman spectroscopy methods for detecting and imaging supported lipid bilayers

2.2 Properties of Water

Transcription:

Supporting Information The Transport and Organization of Cholesterol in Planar Solid-Supported Lipid Bilayer Depend on the Phospholipid Flip-Flop Rate Ting Yu, 1,2 Guangnan Zhou, 1 Xia Hu, 1,2 Shuji Ye 1,2,* 1 Hefei National Laboratory for Physical Sciences at the Microscale, and Department of Chemical Physics, and 2 Synergetic Innovation Center of Quantum Information & Quantum Physics, University of Science and Technology of China, Hefei, nhui 230026, China 1. SFG-VS Experiments. Details regarding SFG theories and instruments have been reported previously. 1-5 In briefly, SFG is composed of a fixed visible beam (532 nm) and tunable IR laser beam (1000~4000 nm). The energy of visible beam and IR beam at 2000-2300cm -1 and 2800-3000 cm -1 is about 10 µj and 40~50µJ, respectively. The incidence angle at CaF 2 surface was 53 for the IR beam and 63 for the visible beam. The SFG setup is similar to that described in our earlier publications. 6, 7 2. Fitting of SFG-VS Signals. s described in detail elsewhere, the intensity of the SFG light is related to the square of the sample's second-order nonlinear susceptibility( χ ), and the intensity of the two input fields I( ωir ) and I ( ω vis ), see eq. (S1), which vanishes when a material has inversion symmetry. 1-5 2 ( SFG eff 1 vis 2 I ω ) χ I ( ω ) I ( ω ) (1) IR eff where ω = ω + ω. The frequency dependence of SFG IR vis χ eff is described by eq. (S2) S1

χ eff ( ω) = χ NR + χ Re s = χ NR + ω ω + iγ where, ω, and Γ are the strength, resonant frequency, and damping coefficient of the vibrational mode(ν), respectively. χ NR and χ Re s are the non-resonant background and the resonant signals of the vibrational mode(ν). could be either positive or negative depending on the phase of the vibrational mode. s the IR beam frequency is tuned over the vibrational resonance of surface/interface molecules, the resonant signals χ Re s can be enhanced. The plot of SFG signal vs. the IR input frequency shows a polarized vibrational spectrum of the molecules at surface or interface., ω, and Γ can be extracted by fitting the spectrum. 3. The possible forms in the organizations of cholesterol in lipid bilayer Figure S1. Six possible forms in the organizations of cholesterol in lipid bilayer in equilibrium. Because the organizations in head to tail and head to head manners don t favor the van der Waals interactions and facilitate the maximal molecular packing, we do not list them in the possible forms. S2

In Figure S1, cholesterol is a molecule comprising a flexible isooctyl hydrocarbon tail and a near planar steroid ring (denoted as the head of cholesterol). The plane of the steroid ring is asymmetric. We refer the flat and smooth side without substituents as the α face and the rough side with substituents of chiral methyl groups as β face. In Figure S1a, S1b and S1c, the cholesterol is only distributed in one leaflet of the bilayer, the ssp or ppp signals of methyl group in the isooctyl hydrocarbon tail cannot be cancelled. In Figure S1d, S1e, and S1f, cholesterol flips from one leaflet to another leaflet and organizes itself in tail to tail manner, the achiral ssp or ppp signals from the methyl groups in the tail can be effectively canceled. In Figure S1b, S1c, and S1d, the methyl substituents in the cholesterol pair orient in the opposite direction, therefore, the chiral psp signals from the methyl substituents of sterol ring can be effectively eliminated with the formation of α-α and β-β structures. In contrast, in Figure S1a, S1e and S1f, the cholesterol pair forms α-β structures, and the methyl substituents in the cholesterol pair orient in the same direction. Therefore, such α-β structures will have large chiral psp signals. Here, the side-by-side organizations of the α-α, β-β and α-β structures are α face by α face, β face by β face, and α face by β face, respectively. 4. The molecular structure of phospholipids. 1,2-dimyristoyl-sn-glycerol-3-phosphocholine (DMPC) 1,2-dipalmitoyl -sn-glycero-3- phosphocholine (DPPC) 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC) S3

1,2-dimyristoyl-d 54 -sn-glycero-3-phosphocholine-1,1,2,2-d 4 -N,N,N-trimethyl-d 9 (d-dmpc) 1,2-dipalmitoyl-d 62 -sn-glycero-3-phosphocholine-1,1,2,2-d 4 -N,N,N-trimethyl-d 9 (d-dppc) 1,2-distearoyl-d 70 -sn-glycero-3-phosphocholine-1,1,2,2-d 4 -N,N,N-trimethyl-d 9 (d-dspc) 1,2-dimyristoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium salt) (DMPG) 1,2-dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium salt) (DPPG) 1,2-distearoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium salt) (DSPG) S4

1,2-dimyristoyl-d 54 -sn-glycero-3-[phospho-rac-(1-glycerol)] (sodium salt) (d-dmpg) 1,2-dipalmitoyl-d 62 -sn-glycero-3-[phospho-rac-(1-glycerol)] (sodium salt) (d-dppg) 1,2-distearoyl-d 70 -sn-glycero-3-[phospho-rac-(1-glycerol)] (sodium salt) (d-dspg) Figure S2. The molecular of cholesterol(chol), cholesterol-d 7 (d-chol) and all the used lipids. 5. The ssp spectra in the frequency range of 1950-2300 cm -1 for the phospholipid monolayer in the air surface. 3 2 1 0 2 1 0 2 1 0 c) Wavenumber (cm -1 ) d) e) f) Wavenumber (cm -1 ) 0.06 0.06 0.06 g) h) i) Wavenumber (cm -1 ) Figure S3. The ssp spectra in the frequency range of 1950-2300 cm -1 for the phospholipid monolayer in the air surface. DMPC; DPPC; c) DSPC; d) d-dmpc; e) d-dppc; f) d-dspc; g) d-dmpg; h) d-dppg; i) d-dspg. S5

6. The SFG spectra from DXPC/(DPPC+d-Chol) and d-dxpc/(dppc+chol). 5 0 5 0 5 0 0.04 B C 5 0 Time(min) Wavenumber(cm -1 ) Wavenumber(cm -1 ) Figure S4.) The time-dependence of the ssp SFG intensity at 2075 cm -1 during the formation of the lipid bilayer. B) The ssp SFG spectra in the frequency region from 1950-2300 cm -1 after flip-flop reaches equilibrium. C) The ppp SFG spectra in the frequency region from 1950-2300 cm -1 after flip-flop reaches equilibrium. DMPC/(DPPC+d-Chol); DPPC/(DPPC+d-Chol). 5 0 5 0 5 0 0 5 0 5 0 Time(min) 0.06 0.05 0.04 8 6 4 2 0 B Wavenumber(cm -1 ) 0.20 0.15 0.10 0.05 0.04 C Wavenumber(cm -1 ) Figure S5.) The time-dependence of the ssp SFG intensity at 2075 cm -1 during the formation of the lipid bilayer. B) The ssp SFG spectra in the frequency region from 1950-2300 cm -1 after flip-flop reaches equilibrium. C) The ppp SFG spectra in the frequency region from 1950-2300 cm -1 after flip-flop reaches equilibrium. d-dmpc /(DPPC+Chol); d-dppc/(dppc+ Chol). S6

7. The surface pressure-area (π-) isotherms of d-dspc and DSPC at air/di water interface. Surface pressure (mn/m) 60 50 40 30 20 10 0 DSPC d-dspc 40 50 60 70 Mean molecular area( 2 /molecule) Figure S6. The surface pressure-area (π-) isotherms of d-dspc and DSPC at air/di water interface at 24 C. Because of isotopic effect, the surface molecular density of d-dspc is larger than DSPC at the surface pressure of 35 mn/m, at which the monolayer was deposited on CaF 2 surface. 8. The time-dependence of the ssp SFG intensity at 2075 cm -1 of d-dppc/(dppc+chol) and d-dppc/dppc. SFG intersity 0.10 0.05 Time(min ) Figure S7. The time-dependence of the ssp SFG intensity at 2075 cm -1 from the CD 3 group of the lipid. d-dppc/(dppc+chol); d-dppc/dppc. From the picture, we can see the flip-flop rate of d-dppc in bilayer d-dppc/(dppc+chol) is much faster than the one in the bilayer of d-dppc/dppc, suggesting the cholesterol S7

facilitates the flip-flop of lipids in the neutral phospholipid bilayer. 9. The lipid and cholesterol show a synchronous flip-flop behavior in the bilayer. Time(min) Figure S8. The time-dependence of the ssp SFG intensity at 2075 cm -1 from the CD 3 group of the bilayer: DPPG/(DPPC+d-Chol); d-dppg/dppc. The intensity (red curve) from d-dppg is divided by 10. 10. The static spectra in equilibrium from d-chol after DPPG/(DMPC+d-Chol) and d-dppg/dmpc at the 0.05mol/L KCl subphase 5 0 5 0 0.08 0.04 ssp ppp Wavenumber ( cm -1 ) 0.20 0.15 0.10 0.05 0.20 0.15 0.10 0.05 B ssp ppp Wavenumber ( cm -1 ) Figure S9. ) The ssp and ppp SFG spectra from d-chol after DPPG/(DMPC+d-Chol) flip-flop reaches equilibrium at the 0.05mol/L KCl subphase. B) The ssp and ppp SFG spectra from d-dppg after d-dppg/dmpc flip-flop reaches equilibrium at the 0.05mol/L KCl subphase. S8

11. The time-dependence of the ssp SFG intensity at 2075 cm -1 of d-dxpg/dmpc and d-dxpg/(dmpc+chol) (Here, X=P or S). 0.3 0.3 c) 0.2 0.2 0.1 0.0 0.3 0.2 0.1 0.1 0.0 0.2 0.1 d) 0.0 Time ( min ) 0.0 Time ( min ) Figure S10. The time-dependence of the ssp SFG intensity at 2075 cm -1 from the CD 3 group in the bilayers of d-dxpg/dmpc and d-dxpg/(dmpc+chol).. d-dppg/dmpc;. d-dppg/(dmpc+chol); c). d-dspg/dmpc; d). d-dspg/(dmpc+chol) For d-dppg/dmpc and d-dppg/(dmpc+chol), the ssp SFG intensity at 2075 cm -1 from the CD 3 group of d-dppg in bilayers, the lipid d-dppg shows almost the same flip-flop rates in the bilayers of d-dppg/dmpc and d-dppg/(dmpc+chol). But it is different from the cholesterol in d-dxpc/(dxpc+chol) bilayer,the cholesterol does not accelerate the lipid flip-flop in negative lipid bilayer. The d-dspg/dmpc and d-dspg/(dmpc+chol) also shows the same conclusion. S9

12. The control experiments on the single component bilayer. 4 2 0 2 0 2 0 2 c) d) 0 2800 2900 3000 3100 Wavenumber (cm -1 ) Figure S11. The chiral psp spectra for the control experiments on the single component bilayer. DMPC/DMPC; DPPC/DMPC; c) DMPC/DPPC; d) DPPC/DPPC. No chiral signal is detected. 13. The psp spectra from 2800-3100 cm -1 of DMPC/(DMPC:d-Chol=1:2). 9 6 3 psp 0 2800 2900 3000 3100 Wavenumber ( cm -1 ) Figure S12. The psp SFG spectra from d-chol in PC: d-chol=1:2 mixtures. Reference: (1) Castellana, E. T.; Cremer, P. S. Solid Supported Lipid Bilayers: From Biophysical Studies to Sensor Design. Surf. Sci. Rep. 2006, 61, 429-444. Shen, Y. R. The Principles of Nonlinear Optics; Wiley: New York, 1984. S10

(3) Lambert,.; Davies, P.; Neivandt, D. Implementing the Theory of Sum Frequency Generation Vibrational Spectroscopy: Tutorial Review. ppl. Spectrosc. Rev. 2005, 40, 103-145. (4) Gopalakrishnan, S.; Liu, D.; llen, H. C.; Kuo, M.; Shultz, M. J. Vibrational Spectroscopic Studies of queous Interfaces: Salts, cids, Bases, and Nanodrops. Chem. Rev. 2006, 106, 1155-1175. (5) Wang, H. F.; Gan, W.; Lu, R.; Rao, Y.; Wu, B.-H. Quantitative Spectral and Orientational nalysis in Surface Sum Frequency Generation Vibrational Spectroscopy (SFG-VS). Int. Rev. Phys. Chem. 2005, 24, 191-256. (6) Ye, S.J.; Wei, F. n pproach to Compatible Multiple Nonlinear Vibrational Spectroscopy Measurements Using Commercial Sum Frequency Generation System. nalyst 2011, 136, 2489-2494. (7) Ye, S. J.; Liu, G. M.; Li, H. C.; Chen, F. G.; Wang, X. W. Effect of dehydration on the interfacial water structure at a charged polymer surface: Negligible χ (3) contribution to sum frequency generation signal. Langmuir 2012, 28, 1374-1380. S11