Literature DB >> 22098740

Measurement of lipid nanodomain (raft) formation and size in sphingomyelin/POPC/cholesterol vesicles shows TX-100 and transmembrane helices increase domain size by coalescing preexisting nanodomains but do not induce domain formation.

Priyadarshini Pathak1, Erwin London.   

Abstract

Mixtures of unsaturated lipids, sphingolipids, and cholesterol form coexisting liquid-disordered and sphingolipid and cholesterol-rich liquid-ordered (Lo) phases in water. The detergent Triton X-100 does not readily solubilize Lo domains, but does solubilize liquid-disordered domains, and is commonly used to prepare detergent-resistant membranes from cells and model membranes. However, it has been proposed that in membranes with mixtures of sphingomyelin (SM), 1-palmitoyl 2-oleoyl phosphatidylcholine (POPC), and cholesterol Triton X-100 may induce Lo domain formation, and therefore detergent-resistant membranes may not reflect the presence of preexisting domains. To examine this hypothesis, the effect of Triton on Lo domain formation was measured in SM/POPC/cholesterol vesicles. Nitroxide quenching methods that can detect ordered nanodomains with radii >12 Å showed that in the absence of Triton X-100 this mixture formed ordered state domains that melt with a midpoint (= T(mid)) at ∼45°C. However, T(mid) was lower when detected using various fluorescence resonance energy transfer (FRET) pairs. Furthermore, the T(mid) value was Ro dependent, and decreased as Ro increased. Because FRET can only readily detect domains with radii >Ro, this result can be explained by domain radii that are close to Ro and decrease as temperature increases. An analysis of FRET and quenching data suggests that nanodomain radius gradually decreases from ≥150 Å to <40 Å as temperature increases from 10 to 45°C. Interestingly, the presence of Triton X-100 or a transmembrane-type peptide did not stabilize ordered state formation when detected by nitroxide quenching, i.e., did not increase T(mid). However, FRET-detected T(mid) did increase in the presence of Triton X-100 or a transmembrane peptide, indicating that both increased domain size. Controls showed that the results could not be accounted for by probe-induced perturbations. Thus, SM/POPC/cholesterol, a mixture similar to that in the outer leaflet of plasma membranes, forms nanodomains at physiological temperatures, and TX-100 does not induce domain formation or increase the fraction of the bilayer in the ordered state, although it does increase domain size by coalescing preexisting domains.
Copyright © 2011 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 22098740      PMCID: PMC3218341          DOI: 10.1016/j.bpj.2011.08.059

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  28 in total

1.  Partitioning of Thy-1, GM1, and cross-linked phospholipid analogs into lipid rafts reconstituted in supported model membrane monolayers.

Authors:  C Dietrich; Z N Volovyk; M Levi; N L Thompson; K Jacobson
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-04       Impact factor: 11.205

2.  Triton promotes domain formation in lipid raft mixtures.

Authors:  H Heerklotz
Journal:  Biophys J       Date:  2002-11       Impact factor: 4.033

Review 3.  Insolubility of lipids in triton X-100: physical origin and relationship to sphingolipid/cholesterol membrane domains (rafts).

Authors:  E London; D A Brown
Journal:  Biochim Biophys Acta       Date:  2000-11-23

4.  Exclusion of a transmembrane-type peptide from ordered-lipid domains (rafts) detected by fluorescence quenching: extension of quenching analysis to account for the effects of domain size and domain boundaries.

Authors:  Michael E Fastenberg; Hidehiko Shogomori; Xiaolian Xu; Deborah A Brown; Erwin London
Journal:  Biochemistry       Date:  2003-10-28       Impact factor: 3.162

5.  Comparison of three ternary lipid bilayer mixtures: FRET and ESR reveal nanodomains.

Authors:  Frederick A Heberle; Jing Wu; Shih Lin Goh; Robin S Petruzielo; Gerald W Feigenson
Journal:  Biophys J       Date:  2010-11-17       Impact factor: 4.033

6.  Lipid rafts reconstituted in model membranes.

Authors:  C Dietrich; L A Bagatolli; Z N Volovyk; N L Thompson; M Levi; K Jacobson; E Gratton
Journal:  Biophys J       Date:  2001-03       Impact factor: 4.033

7.  Fluorescence energy transfer reveals microdomain formation at physiological temperatures in lipid mixtures modeling the outer leaflet of the plasma membrane.

Authors:  John R Silvius
Journal:  Biophys J       Date:  2003-08       Impact factor: 4.033

8.  The sensitivity of lipid domains to small perturbations demonstrated by the effect of Triton.

Authors:  Heiko Heerklotz; Halina Szadkowska; Thomas Anderson; Joachim Seelig
Journal:  J Mol Biol       Date:  2003-06-13       Impact factor: 5.469

9.  Preparation and properties of asymmetric vesicles that mimic cell membranes: effect upon lipid raft formation and transmembrane helix orientation.

Authors:  Hui-Ting Cheng; Erwin London
Journal:  J Biol Chem       Date:  2009-01-07       Impact factor: 5.157

10.  Steroid structural requirements for stabilizing or disrupting lipid domains.

Authors:  Jorge J Wenz; Francisco J Barrantes
Journal:  Biochemistry       Date:  2003-12-09       Impact factor: 3.162

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  55 in total

1.  Induction of Ordered Lipid Raft Domain Formation by Loss of Lipid Asymmetry.

Authors:  Johnna Wellman St Clair; Shinako Kakuda; Erwin London
Journal:  Biophys J       Date:  2020-07-10       Impact factor: 4.033

2.  Impact of Acyl Chain Mismatch on the Formation and Properties of Sphingomyelin-Cholesterol Domains.

Authors:  Thomas K M Nyholm; Oskar Engberg; Victor Hautala; Hiroshi Tsuchikawa; Kai-Lan Lin; Michio Murata; J Peter Slotte
Journal:  Biophys J       Date:  2019-09-25       Impact factor: 4.033

3.  DHA Modifies the Size and Composition of Raftlike Domains: A Solid-State 2H NMR Study.

Authors:  Jacob J Kinnun; Robert Bittman; Saame Raza Shaikh; Stephen R Wassall
Journal:  Biophys J       Date:  2018-01-23       Impact factor: 4.033

Review 4.  Protein-lipid interactions critical to replication of the influenza A virus.

Authors:  Petr Chlanda; Joshua Zimmerberg
Journal:  FEBS Lett       Date:  2016-03-30       Impact factor: 4.124

5.  Changes in glucosylceramide structure affect virulence and membrane biophysical properties of Cryptococcus neoformans.

Authors:  Shriya Raj; Saeed Nazemidashtarjandi; Jihyun Kim; Luna Joffe; Xiaoxue Zhang; Ashutosh Singh; Visesato Mor; Desmarini Desmarini; Julianne Djordjevic; Daniel P Raleigh; Marcio L Rodrigues; Erwin London; Maurizio Del Poeta; Amir M Farnoud
Journal:  Biochim Biophys Acta Biomembr       Date:  2017-09-01       Impact factor: 3.747

6.  Lipid nanodomains change ion channel function.

Authors:  Michael Weinrich; David L Worcester; Sergey M Bezrukov
Journal:  Nanoscale       Date:  2017-09-14       Impact factor: 7.790

7.  Altering hydrophobic sequence lengths shows that hydrophobic mismatch controls affinity for ordered lipid domains (rafts) in the multitransmembrane strand protein perfringolysin O.

Authors:  Qingqing Lin; Erwin London
Journal:  J Biol Chem       Date:  2012-11-13       Impact factor: 5.157

8.  Toward a better raft model: modulated phases in the four-component bilayer, DSPC/DOPC/POPC/CHOL.

Authors:  Shih Lin Goh; Jonathan J Amazon; Gerald W Feigenson
Journal:  Biophys J       Date:  2013-02-19       Impact factor: 4.033

9.  Sterol Structure Strongly Modulates Membrane-Islet Amyloid Polypeptide Interactions.

Authors:  Xiaoxue Zhang; Erwin London; Daniel P Raleigh
Journal:  Biochemistry       Date:  2018-03-12       Impact factor: 3.162

10.  Lipid rafts can form in the inner and outer membranes of Borrelia burgdorferi and have different properties and associated proteins.

Authors:  Alvaro Toledo; Zhen Huang; James L Coleman; Erwin London; Jorge L Benach
Journal:  Mol Microbiol       Date:  2018-02-15       Impact factor: 3.501

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