Abstract

Here we report the results of shear-mode thicknesses and absorption coefficient measurements made on neat membranes using scanning near-field optical microscopy (SNOM). Biomimic neat membranes composed of two different types of phoshpholipid molecules: 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) and 1,2- dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) were found to exhibit different absorption coefficients under the SNOM. The localization of the lipids could be identified and correlated to the morphology of the membrane domains indicating that SNOM can be an effective and accurate approach for the label-free characterization of the structure-function relationships in cell membranes.

© 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement

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2018 (1)

A. Cernescu, M. Szuwarzyński, U. Kwolek, P. Wydro, M. Kepczynski, S. Zapotoczny, M. Nowakowska, and L. Quaroni, “Label-Free Infrared Spectroscopy and Imaging of Single Phospholipid Bilayers with Nanoscale Resolution,” Anal. Chem. 90(17), 10179–10186 (2018).
[Crossref]

2017 (5)

I. Y. Hasan and A. Mechler, “Nanoviscosity measurements revealing domain formation in biomimetic membranes,” Anal. Chem. 89(3), 1855–1862 (2017).
[Crossref]

L. Almonte and J. Colchero, “True non-contact atomic force microscopy imaging of heterogeneous biological samples in liquids: topography and material contrast,” Nanoscale 9(8), 2903–2915 (2017).
[Crossref]

I. Y. Hasan and A. Mechler, “Analytical approaches to study domain formation in biomimetic membranes,” Analyst 142(17), 3062–3078 (2017).
[Crossref]

R. Regmi, P. M. Winkler, V. Flauraud, K. J. Borgman, C. Manzo, J. Brugger, H. Rigneault, J. Wenger, and M. F. García-Parajo, “Planar optical nanoantennas resolve cholesterol-dependent nanoscale heterogeneities in the plasma membrane of living cells,” Nano Lett. 17(10), 6295–6302 (2017).
[Crossref]

M. Bodescu, F. Rosenkötter, and J. Fritz, “Time lapse AFM on vesicle formation from mixed lipid bilayers induced by the membrane–active peptide melittin,” Soft Matter 13(38), 6845–6851 (2017).
[Crossref]

2016 (3)

K.-D. Park, M. B. Raschke, M. J. Jang, J. H. Kim, and B-H. O., S-G. Park, E-H. Lee, and S. G. Lee, “Near-Field Imaging of Cell Membranes in Liquid Enabled by Active Scanning Probe Mechanical Resonance Control,” J. Phys. Chem. C 120(37), 21138–21144 (2016).
[Crossref]

K.-D. Park, M. B. Raschke, M. J. Jang, J. H. Kim, and B-H. O., S-G. Park, E-H. Lee, and S. G. Lee, “Near-Field Imaging of Cell Membranes in Liquid Enabled by Active Scanning Probe Mechanical Resonance Control,” J. Phys. Chem. C 120(37), 21138–21144 (2016).
[Crossref]

S. Spindler, J. Ehrig, K. König, T. Nowak, M. Piliarik, H. E. Stein, R. W. Taylor, E. Garanger, S. Lecommandoux, I. D. Alves, and V. Sandoghdar, “Visualization of lipids and proteins at high spatial and temporal resolution via interferometric scattering (iSCAT) microscopy,” J. Phys. D: Appl. Phys. 49(27), 274002 (2016).
[Crossref]

H. M. Wu, Y. H. Lin, T. C. Yen, and C. L. Hsieh, “Nanoscopic substructures of raft-mimetic liquid-ordered membrane domains revealed by high-speed single-particle tracking,” Sci. Rep. 6(1), 20542 (2016).
[Crossref]

2015 (1)

I. Y. Hasan and A. Mechler, “Viscoelastic changes measured in partially suspended single bilayer membranes,” Soft Matter 11(27), 5571–5579 (2015).
[Crossref]

2014 (1)

J. Lü, J. Yang, M. Dong, and O. Sahin, “Nanomechanical spectroscopy of synthetic and biological membranes,” Nanoscale 6(13), 7604–7608 (2014).
[Crossref]

2013 (4)

S. Berweger, Duc M. Nguyen, Eric A. Muller, Hans A. Bechtel, Thomas T. Perkins, and Markus B. Raschke, “Nano-Chemical Infrared Imaging of Membrane Proteins in Lipid Bilayers,” J. Am. Chem. Soc. 135(49), 18292–18295 (2013).
[Crossref]

G. J. Hardy, R. Nayak, and S. Zauscher, “Model cell membranes: Techniques to form complex biomimetic supported lipid bilayers via vesicle fusion,” Curr. Opin. Colloid Interface Sci. 18(5), 448–458 (2013).
[Crossref]

S. Attwood, Y. Choi, and Z. Leonenko, “Preparation of DOPC and DPPC supported planar lipid bilayers for atomic force microscopy and atomic force spectroscopy,” Int. J. Mol. Sci. 14(2), 3514–3539 (2013).
[Crossref]

H. Chang-Chun, Z. Lei, S. Run-Guang, Z. Jing, H. Guang-Xiao, and Y. Jing, “Molecular Interaction and Morphology of DOPC/DPPC Monolayer,” Chem J Chinese U 34(10), 2340–2346 (2013).
[Crossref]

2012 (2)

T. J. Allen, P. C. Beard, A. Hall, A. P. Dhillon, and J. S. Owen, “Spectroscopic photoacoustic imaging of lipid-rich plaques in the human aorta in the 740 to 1400 nm wavelength range,” J. Biomed. Opt. 17(6), 061209 (2012).
[Crossref]

M. Cai, W. Zhao, X. Shang, J. Jiang, H. Ji, Z. Tang, and H. Wang, “Direct evidence of lipid rafts by in situ atomic force microscopy,” Small 8(8), 1243–1250 (2012).
[Crossref]

2010 (3)

M. C. Giocondi, D. Yamamoto, E. Lesniewska, P. E. Milhiet, T. Ando, and C. Le Grimellec, “Surface topography of membrane domains,” Biochim. Biophys. Acta, Biomembr. 1798(4), 703–718 (2010).
[Crossref]

D. Lingwood and K. Simons, “Lipid rafts as a membrane-organizing principle,” Science 327(5961), 46–50 (2010).
[Crossref]

K. El Kirat, S. Morandat, and Y. F. Dufrêne, “Nanoscale analysis of supported lipid bilayers using atomic force microscopy,” Biochim. Biophys. Acta, Biomembr. 1798(4), 750–765 (2010).
[Crossref]

2009 (2)

C. Eggeling, C. Ringemann, R. Medda, G. Schwarzmann, K. Sandhoff, S. Polyakova, V. N. Belov, B. Hein, C. Von Middendorff, A. Schönle, and S. W. Hell, “Direct observation of the nanoscale dynamics of membrane lipids in a living cell,” Nature 457(7233), 1159–1162 (2009).
[Crossref]

A. Mechler, S. Praporski, S. Piantavigna, S. M. Heaton, K. N. Hall, M. I. Aguilar, and L. L. Martin, “Structure and homogeneity of pseudo-physiological phospholipid bilayers and their deposition characteristics on carboxylic acid terminated self-assembled monolayers,” Biomaterials 30(4), 682–689 (2009).
[Crossref]

2008 (4)

M. P. Mingeot-Leclercq, M. Deleu, R. Brasseur, and Y. F. Dufrêne, “Atomic force microscopy of supported lipid bilayers,” Nat. Protoc. 3(10), 1654–1659 (2008).
[Crossref]

G. Van Meer, D. R. Voelker, and G. W. Feigenson, “Membrane lipids: where they are and how they behave,” Nat. Rev. Mol. Cell Biol. 9(2), 112–124 (2008).
[Crossref]

J. Generosi, G. Margaritondo, J. S. Sanghera, I. D. Aggarwal, N. H. Tolk, D. W. Piston, A. C. Castellano, and A. Cricenti, “Infrared scanning near-field optical microscopy investigates order and clusters in model membranes,” J. Microsc. 229(2), 259–263 (2008)..
[Crossref]

D. V. Serebryakov, S. K. Sekatskii, A. P. Cherkun, K. Dukenbayev, I. V. Morozov, V. S. Letokhov, and G. Dietler, “Scanning near-field optical microscope based on a double resonant fibre probe montage and equipped with time-gated photon detection,” J. Microsc. 229(2), 287–292 (2008)..
[Crossref]

2007 (5)

M. C. Howland, A. W. Szmodis, B. Sanii, and A. N. Parikh, “Characterization of physical properties of supported phospholipid membranes using imaging ellipsometry at optical wavelengths,” Biophys. J. 92(4), 1306–1317 (2007).
[Crossref]

A. J. García-Sáez, S. Chiantia, and P. Schwille, “Effect of line tension on the lateral organization of lipid membranes,” J. Biol. Chem. 282(46), 33537–33544 (2007).
[Crossref]

S. Chiantia, N. Kahya, and P. Schwille, “Raft domain reorganization driven by short-and long-chain ceramide: a combined AFM and FCS study,” Langmuir 23(14), 7659–7665 (2007).
[Crossref]

R. F. De Almeida, J. Borst, A. Fedorov, M. Prieto, and A. J. Visser, “Complexity of lipid domains and rafts in giant unilamellar vesicles revealed by combining imaging and microscopic and macroscopic time-resolved fluorescence,” Biophys. J. 93(2), 539–553 (2007).
[Crossref]

L. J. Johnston, “Nanoscale imaging of domains in supported lipid membranes,” Langmuir 23(11), 5886–5895 (2007).
[Crossref]

2006 (2)

R. P. Richter, R. Bérat, and A. R. Brisson, “Formation of solid-supported lipid bilayers: an integrated view,” Langmuir 22(8), 3497–3505 (2006).
[Crossref]

P. Janmey and P. Kinnunen, “Biophysical properties of lipids and dynamic membranes,” Trends Cell Biol. 16(10), 538–546 (2006).
[Crossref]

2005 (1)

R. L. P. Van Veen, H. J. Sterenborg, A. Pifferi, A. Torricelli, E. Chikoidze, and R. Cubeddu, “Determination of visible near-IR absorption coefficients of mammalian fat using time-and spatially resolved diffuse reflectance and transmission spectroscopy,” J. Biomed. Opt. 10(5), 054004 (2005).
[Crossref]

2004 (1)

Z. V. Leonenko, E. Finot, H. Ma, T. E. S. Dahms, and D. T. Cramb, “Investigation of temperature-induced phase transitions in DOPC and DPPC phospholipid bilayers using temperature-controlled scanning force microscopy,” Biophys. J. 86(6), 3783–3793 (2004).
[Crossref]

2003 (1)

S. L. Veatch and S. L. Keller, “Separation of liquid phases in giant vesicles of ternary mixtures of phospholipids and cholesterol,” Biophys. J. 85(5), 3074–3083 (2003).
[Crossref]

2001 (1)

M. C. Giocondi, V. Vié, E. Lesniewska, P. E. Milhiet, M. Zinke-Allmang, and C. Le Grimellec, “Phase topology and growth of single domains in lipid bilayers,” Langmuir 17(5), 1653–1659 (2001).
[Crossref]

2000 (1)

A. Pralle, P. Keller, E. L. Florin, K. Simons, and J. H. Hörber, “Sphingolipid–cholesterol rafts diffuse as small entities in the plasma membrane of mammalian cells,” J. Cell Biol. 148(5), 997–1008 (2000).
[Crossref]

1999 (2)

R. C. Dunn, “Near-field scanning optical microscopy,” Chem. Rev. 99(10), 2891–2928 (1999).
[Crossref]

B. Knoll and F. Keilmann, “Near-field probing of vibrational absorption for chemical microscopy,” Nature 399(6732), 134 (1999).
[Crossref]

1998 (1)

1994 (1)

A. S. Ulrich, M. Sami, and A. Watts, “Hydration of DOPC bilayers by differential scanning calorimetry,” Biochim. Biophys. Acta, Biomembr. 1191(1), 225–230 (1994).
[Crossref]

1993 (1)

R. L. Biltonen and D. Lichtenberg, “The use of differential scanning calorimetry as a tool to characterize liposome preparations,” Chem. Phys. Lipids 64(1-3), 129–142 (1993).
[Crossref]

1992 (1)

E. Kalb, S. Frey, and L. K. Tamm, “Formation of supported planar bilayers by fusion of vesicles to supported phospholipid monolayers,” Biochim. Biophys. Acta, Biomembr. 1103(2), 307–316 (1992).
[Crossref]

1991 (2)

E. J. K. T. D. J. S. R. L. Betzig, J. K. Trautman, T. D. Harris, J. S. Weiner, and R. L. Kostelak, “Breaking the diffraction barrier: optical microscopy on a nanometric scale,” Science 251(5000), 1468–1470 (1991).
[Crossref]

W. Hübner and H. H. Mantsch, “Orientation of specifically 13C = O labeled phosphatidylcholine multilayers from polarized attenuated total reflection FT-IR spectroscopy,” Biophys. J. 59(6), 1261–1272 (1991).
[Crossref]

1987 (1)

E. Betzig, M. Isaacson, and A. Lewis, “Collection mode near-field scanning optical microscopy,” Appl. Phys. Lett. 51(25), 2088–2090 (1987).
[Crossref]

1986 (1)

E. Betzig, A. Lewis, A. Harootunian, M. Isaacson, and E. Kratschmer, “Near field scanning optical microscopy (NSOM): development and biophysical applications,” Biophys. J. 49(1), 269–279 (1986).
[Crossref]

1977 (1)

J. N. Israelachvili, D. J. Mitchell, and B. W. Ninham, “Theory of self-assembly of lipid bilayers and vesicles,” Biochim. Biophys. Acta, Biomembr. 470(2), 185–201 (1977).
[Crossref]

Aggarwal, I. D.

J. Generosi, G. Margaritondo, J. S. Sanghera, I. D. Aggarwal, N. H. Tolk, D. W. Piston, A. C. Castellano, and A. Cricenti, “Infrared scanning near-field optical microscopy investigates order and clusters in model membranes,” J. Microsc. 229(2), 259–263 (2008)..
[Crossref]

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A. Mechler, S. Praporski, S. Piantavigna, S. M. Heaton, K. N. Hall, M. I. Aguilar, and L. L. Martin, “Structure and homogeneity of pseudo-physiological phospholipid bilayers and their deposition characteristics on carboxylic acid terminated self-assembled monolayers,” Biomaterials 30(4), 682–689 (2009).
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Figures (5)

Fig. 1.
Fig. 1. (a) Collection-mode SNOM imaging of the Pt/C chevron sample. Simultaneously acquired (a) topography (in nm) and corresponding (b) optical transmission images (in V) of the same sample. Scale bar length is 5 µm. (c) Representative topography (red) and transmission (blue) profiles along line #1 in the respective image pairs.
Fig. 2.
Fig. 2. (a) Collection-mode SNOM imaging of the DPPC (a, b and c) and DOPC (d, e and f) -based single bilayer membrane patches. Simultaneously acquired (a, d) topography (in nm) and (b, e) light transmission intensity images (in a.u.) of the same membrane patches. (c, f) Representative topography (red) and transmission (blue) profiles along line #1 in the respective image pairs.
Fig. 3.
Fig. 3. Blue and red triangles represent the experimental measurements of the absorption coefficients of DOPC and DPPC-based membrane nanodomains, with respect to the thickness of the individual domains.
Fig. 4.
Fig. 4. Blue and red triangles represent the experimental measurements of the absorption coefficients of DOPC and DPPC-based membrane nanodomains in a narrow thickness range (For DOPC: within 5 ∼ 6 nm range, and for DPPC: within 9 ∼ 10 nm range) for both collection (close triangles) and illumination (open triangles) mode SNOM imaging.
Fig. 5.
Fig. 5. Collection mode SNOM imaging of the mixed lipid (DPPC:DOPC) patches. (a) Topography and (b) SNOM intensity images showing the domains marked with the arrows within the DPPC:DOPC patches. (c) shows the corresponding profiles of topography and absorption coefficient along line #1 estimated from the respective topography and intensity images. (d) schematic of the lipid domains.

Tables (1)

Tables Icon

Table 1. Measured near-field absorption coefficients for the Pt/C Bars

Equations (1)

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α ( x , y ) = log e ( I m I ( x , y ) ) z ( x , y )