Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2009 Apr 15;131(14):5068-9.
doi: 10.1021/ja9011468.

Loosening and reorganization of fluid phospholipid bilayers by chloroform

Affiliations

Loosening and reorganization of fluid phospholipid bilayers by chloroform

Serhan Turkyilmaz et al. J Am Chem Soc. .

Abstract

The mixing behavior of an exchangeable phospholipid (A) with an exchangeable sterol (B) in host bilayers made from 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) containing varying concentrations of cholesterol has been examined via the nearest-neighbor recognition method. At low sterol concentrations (i.e., 2.5 mol %), the mixing between A and B is close to ideal. Incremental increases in the sterol concentration to 40 mol % led to net increases in the affinity between A and B. Similar mixing experiments that were carried out in the presence of chloroform showed a leveling effect, where moderate sterol-phospholipid affinity was observed in all cases. These results, together with the fact that the number of chloroform molecules that are absorbed per phospholipid is essentially constant and independent of the sterol content, support a model in which chloroform favors solvation of the phospholipids and a common membrane state is produced. Fluorescence measurements and Raman spectra have also shown that chloroform significantly loosens both cholesterol-poor and cholesterol-rich membranes made from DPPC. In a broader context, these results suggest a fundamentally new mechanism of anesthesia, where the anesthetic, by solvating the lipid components, profoundly changes the lateral organization of the lipid framework.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Lipids and reaction vessel used for NNR experiments.
Figure 2
Figure 2
Plot of K versus sterol concentration in (●) the absence and (■) presence of a saturated chloroform atmosphere.
Figure 3
Figure 3
(A) Plot of GP versus temperature in liposomes made from DPPC/DPPG/cholesterol (97.5/2.5/2.5, mol%) without (■) and with (□) CHCl3; DPPC/DPPG/cholesterol (57.5/2.5/40, mol%) without (●) and with (○) CHCl3. (B) Raman spectra at 45°C for liposomes made from (top frame): DPPC/DPPG/cholesterol (97.5/2.5/2.5, mol%) and (bottom frame): DPPC/DPPG/cholesterol (57.5/2.5/40, mol%) without (a and c) and with (b and d) CHCl3.
Scheme 1
Scheme 1

Similar articles

Cited by

References

    1. Bondarenko V, Yushmanov VE, Xu Y, Tang P. Biophys. J. 2008;94:1681–1688. - PMC - PubMed
    1. Peoples RW, Li C, Weight FW. Annu. Rev. Pharmacol. Toxicol. 1996;36:185–201. - PubMed
    1. Cao H, Zhang J, Jing B, Regen SL. J. Am. Chem. Soc. 2005;127:8813–8816. - PubMed
    2. Sugahara M, Uragami M, Regen SL. J. Am. Chem. Soc. 2003;125:13040–13041. - PubMed
    3. Sugahara M, Uragami M, Yan X, Regen SL. J. Am. Chem. Soc. 2001;123:7939–7940. - PubMed
    1. Regen SL. Current Opinion in Chem. Biol. 2002;6:729–735. - PubMed
    1. McIntosh TJ, editor. Lipid Rafts. New York: Springer-Verlag; 2007.
    2. Edidin M. Annu. Rev. Biomol. Struct. 2003;32:257–283. - PubMed

Publication types