Dimyristoylphosphatidylcholine/C16:0-ceramide binary liposomes studied by differential scanning calorimetry and wide- and small-angle X-ray scattering

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Dimyristoylphosphatidylcholine/C16:0-ceramide binary liposomes studied by differential scanning calorimetry and wide- and small-angle X-ray scattering. / Holopainen, Juha M.; Lemmich, Jesper; Richter, Frank; Mouritsen, Ole G.; Rapp, Gert; Kinnunen, Paavo K.J.

In: Biophysical Journal, Vol. 78, No. 5, 01.01.2000, p. 2459-2469.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Holopainen, JM, Lemmich, J, Richter, F, Mouritsen, OG, Rapp, G & Kinnunen, PKJ 2000, 'Dimyristoylphosphatidylcholine/C16:0-ceramide binary liposomes studied by differential scanning calorimetry and wide- and small-angle X-ray scattering', Biophysical Journal, vol. 78, no. 5, pp. 2459-2469. https://doi.org/10.1016/S0006-3495(00)76790-7

APA

Holopainen, J. M., Lemmich, J., Richter, F., Mouritsen, O. G., Rapp, G., & Kinnunen, P. K. J. (2000). Dimyristoylphosphatidylcholine/C16:0-ceramide binary liposomes studied by differential scanning calorimetry and wide- and small-angle X-ray scattering. Biophysical Journal, 78(5), 2459-2469. https://doi.org/10.1016/S0006-3495(00)76790-7

Vancouver

Holopainen JM, Lemmich J, Richter F, Mouritsen OG, Rapp G, Kinnunen PKJ. Dimyristoylphosphatidylcholine/C16:0-ceramide binary liposomes studied by differential scanning calorimetry and wide- and small-angle X-ray scattering. Biophysical Journal. 2000 Jan 1;78(5):2459-2469. https://doi.org/10.1016/S0006-3495(00)76790-7

Author

Holopainen, Juha M. ; Lemmich, Jesper ; Richter, Frank ; Mouritsen, Ole G. ; Rapp, Gert ; Kinnunen, Paavo K.J. / Dimyristoylphosphatidylcholine/C16:0-ceramide binary liposomes studied by differential scanning calorimetry and wide- and small-angle X-ray scattering. In: Biophysical Journal. 2000 ; Vol. 78, No. 5. pp. 2459-2469.

Bibtex

@article{5876c19aff6d40df81305ff17f39cb73,
title = "Dimyristoylphosphatidylcholine/C16:0-ceramide binary liposomes studied by differential scanning calorimetry and wide- and small-angle X-ray scattering",
abstract = "Ceramide has recently been established as a central messenger in the signaling cascades controlling cell behavior. Physicochemical studies have revealed a strong tendency of this lipid toward phase separation in mixtures with phosphatidylcholines. The thermal phase behavior and structure of fully hydrated binary membranes composed of dimyristoylphosphatidylcholine (DMPC) and N-palmitoyl-ceramide (C16:0-ceramide, up to a mole fraction X(cer) = 0.35) were resolved in further detail by high-sensitivity differential scanning calorimetry (DSC) and x-ray diffraction. Both methods reveal very strong hysteresis in the thermal phase behavior of ceramide-containing membranes. A partial phase diagram was constructed based on results from a combination of these two methods. DSC heating scans show that with increased X(cer) the pretransition temperature T(p) first increases, whereafter at X(cer) > 0.06 it can no longer be resolved. The main transition enthalpy ΔH remains practically unaltered while its width increases significantly, and the upper phase boundary temperature of the mixture shifts to ~63°C at X(cer) = 0.30. Upon cooling, profound phase separation is evident, and for all of the studied compositions there is an endotherm in the region close to the T(m) for DMPC. At X(cer) ≥ 0.03 a second endotherm is evident at higher temperatures, starting at 32.1°C and reaching 54.6°C at X(cer) = 0.30. X- ray small-angle reflection heating scans reveal a lamellar phase within the temperature range of 15-60°C, regardless of composition. The pretransition is observed up to X(cer) < 0.18, together with an increase in T(p). In the gel phase the lamellar repeat distance d increases from ~61 {\AA} at X(cer) = 0.03, to 67 {\AA} at X(cer) = 0.35. In the fluid phase increasing X(cer) from 0.06 to 0.35 augments d from 61 {\AA} to 64 {\AA}. An L(β)/L(α) (ripple/fluid) phase coexistence region is observed at high temperatures (from 31 to 56.5°C) when X(cer) > 0.03. With cooling from temperatures above 50°C we observe a slow increase in d as the coexistence region is entered. A sudden solidification into a metastable, modulated gel phase with high d values is observed for all compositions at ~24°C. The anomalous swelling for up to X(cer) = 0.30 in the transition region is interpreted as an indication of bilayer softening and thermally reduced bending rigidity.",
author = "Holopainen, {Juha M.} and Jesper Lemmich and Frank Richter and Mouritsen, {Ole G.} and Gert Rapp and Kinnunen, {Paavo K.J.}",
year = "2000",
month = jan,
day = "1",
doi = "10.1016/S0006-3495(00)76790-7",
language = "English",
volume = "78",
pages = "2459--2469",
journal = "Biophysical Society. Annual Meeting. Abstracts",
issn = "0523-6800",
publisher = "Biophysical Society",
number = "5",

}

RIS

TY - JOUR

T1 - Dimyristoylphosphatidylcholine/C16:0-ceramide binary liposomes studied by differential scanning calorimetry and wide- and small-angle X-ray scattering

AU - Holopainen, Juha M.

AU - Lemmich, Jesper

AU - Richter, Frank

AU - Mouritsen, Ole G.

AU - Rapp, Gert

AU - Kinnunen, Paavo K.J.

PY - 2000/1/1

Y1 - 2000/1/1

N2 - Ceramide has recently been established as a central messenger in the signaling cascades controlling cell behavior. Physicochemical studies have revealed a strong tendency of this lipid toward phase separation in mixtures with phosphatidylcholines. The thermal phase behavior and structure of fully hydrated binary membranes composed of dimyristoylphosphatidylcholine (DMPC) and N-palmitoyl-ceramide (C16:0-ceramide, up to a mole fraction X(cer) = 0.35) were resolved in further detail by high-sensitivity differential scanning calorimetry (DSC) and x-ray diffraction. Both methods reveal very strong hysteresis in the thermal phase behavior of ceramide-containing membranes. A partial phase diagram was constructed based on results from a combination of these two methods. DSC heating scans show that with increased X(cer) the pretransition temperature T(p) first increases, whereafter at X(cer) > 0.06 it can no longer be resolved. The main transition enthalpy ΔH remains practically unaltered while its width increases significantly, and the upper phase boundary temperature of the mixture shifts to ~63°C at X(cer) = 0.30. Upon cooling, profound phase separation is evident, and for all of the studied compositions there is an endotherm in the region close to the T(m) for DMPC. At X(cer) ≥ 0.03 a second endotherm is evident at higher temperatures, starting at 32.1°C and reaching 54.6°C at X(cer) = 0.30. X- ray small-angle reflection heating scans reveal a lamellar phase within the temperature range of 15-60°C, regardless of composition. The pretransition is observed up to X(cer) < 0.18, together with an increase in T(p). In the gel phase the lamellar repeat distance d increases from ~61 Å at X(cer) = 0.03, to 67 Å at X(cer) = 0.35. In the fluid phase increasing X(cer) from 0.06 to 0.35 augments d from 61 Å to 64 Å. An L(β)/L(α) (ripple/fluid) phase coexistence region is observed at high temperatures (from 31 to 56.5°C) when X(cer) > 0.03. With cooling from temperatures above 50°C we observe a slow increase in d as the coexistence region is entered. A sudden solidification into a metastable, modulated gel phase with high d values is observed for all compositions at ~24°C. The anomalous swelling for up to X(cer) = 0.30 in the transition region is interpreted as an indication of bilayer softening and thermally reduced bending rigidity.

AB - Ceramide has recently been established as a central messenger in the signaling cascades controlling cell behavior. Physicochemical studies have revealed a strong tendency of this lipid toward phase separation in mixtures with phosphatidylcholines. The thermal phase behavior and structure of fully hydrated binary membranes composed of dimyristoylphosphatidylcholine (DMPC) and N-palmitoyl-ceramide (C16:0-ceramide, up to a mole fraction X(cer) = 0.35) were resolved in further detail by high-sensitivity differential scanning calorimetry (DSC) and x-ray diffraction. Both methods reveal very strong hysteresis in the thermal phase behavior of ceramide-containing membranes. A partial phase diagram was constructed based on results from a combination of these two methods. DSC heating scans show that with increased X(cer) the pretransition temperature T(p) first increases, whereafter at X(cer) > 0.06 it can no longer be resolved. The main transition enthalpy ΔH remains practically unaltered while its width increases significantly, and the upper phase boundary temperature of the mixture shifts to ~63°C at X(cer) = 0.30. Upon cooling, profound phase separation is evident, and for all of the studied compositions there is an endotherm in the region close to the T(m) for DMPC. At X(cer) ≥ 0.03 a second endotherm is evident at higher temperatures, starting at 32.1°C and reaching 54.6°C at X(cer) = 0.30. X- ray small-angle reflection heating scans reveal a lamellar phase within the temperature range of 15-60°C, regardless of composition. The pretransition is observed up to X(cer) < 0.18, together with an increase in T(p). In the gel phase the lamellar repeat distance d increases from ~61 Å at X(cer) = 0.03, to 67 Å at X(cer) = 0.35. In the fluid phase increasing X(cer) from 0.06 to 0.35 augments d from 61 Å to 64 Å. An L(β)/L(α) (ripple/fluid) phase coexistence region is observed at high temperatures (from 31 to 56.5°C) when X(cer) > 0.03. With cooling from temperatures above 50°C we observe a slow increase in d as the coexistence region is entered. A sudden solidification into a metastable, modulated gel phase with high d values is observed for all compositions at ~24°C. The anomalous swelling for up to X(cer) = 0.30 in the transition region is interpreted as an indication of bilayer softening and thermally reduced bending rigidity.

UR - http://www.scopus.com/inward/record.url?scp=0034105994&partnerID=8YFLogxK

U2 - 10.1016/S0006-3495(00)76790-7

DO - 10.1016/S0006-3495(00)76790-7

M3 - Journal article

C2 - 10777742

AN - SCOPUS:0034105994

VL - 78

SP - 2459

EP - 2469

JO - Biophysical Society. Annual Meeting. Abstracts

JF - Biophysical Society. Annual Meeting. Abstracts

SN - 0523-6800

IS - 5

ER -

ID: 236896142