Literature DB >> 4016202

Effect of divalent cations on the assembly of neutral and charged phospholipid bilayers in patch-recording pipettes.

R Coronado.   

Abstract

Monolayers of the negatively charged phospholipid phosphatidylserine (PS) and of the amphoteric phospholipid dioleoylphosphatidylethanolamine (DOPE) were used to assemble bilayers at the tip of patch-recording pipettes. PS bilayers, with seal resistances in the range of gigaohmns (gigaseals), could only be generated when millimolar concentration of divalent cations, Ca++, Mg++, or Ba++ were present in the pipette and bath solutions. In contrast, gigaseals of DOPE were independent of divalent ion concentration in the pH range where DOPE is predominantly neutral (pH 6.5) or positively charged (pH 1.5). At pH 10.0, when most DOPE molecules bear a net negative charge, gigaseals became divalent cation dependent, in a manner quantitatively similar to that of PS at neutral pH. The results indicate that divalent cations play an important role in stabilizing gigaseals of negatively charged lipid but are of no consequence in neutral or positively charged seals.

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Year:  1985        PMID: 4016202      PMCID: PMC1435169          DOI: 10.1016/S0006-3495(85)83990-4

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


  5 in total

1.  Single-channel recordings from purified acetylcholine receptors reconstituted in bilayers formed at the tip of patch pipets.

Authors:  B A Suarez-Isla; K Wan; J Lindstrom; M Montal
Journal:  Biochemistry       Date:  1983-05-10       Impact factor: 3.162

2.  Melittin and a chemically modified trichotoxin form alamethicin-type multi-state pores.

Authors:  W Hanke; C Methfessel; H U Wilmsen; E Katz; G Jung; G Boheim
Journal:  Biochim Biophys Acta       Date:  1983-01-05

3.  Phospholipid bilayers made from monolayers on patch-clamp pipettes.

Authors:  R Coronado; R Latorre
Journal:  Biophys J       Date:  1983-08       Impact factor: 4.033

4.  Surface charge and the conductance of phospholipid membranes.

Authors:  S G McLaughlin; G Szabo; G Eisenman; S M Ciani
Journal:  Proc Natl Acad Sci U S A       Date:  1970-11       Impact factor: 11.205

5.  Divalent ions and the surface potential of charged phospholipid membranes.

Authors:  S G McLaughlin; G Szabo; G Eisenman
Journal:  J Gen Physiol       Date:  1971-12       Impact factor: 4.086

  5 in total
  7 in total

1.  Curvature-electric effects in artificial and natural membranes studied using patch-clamp techniques.

Authors:  A G Petrov; R L Ramsey; P N Usherwood
Journal:  Eur Biophys J       Date:  1989       Impact factor: 1.733

2.  A pressure-polishing set-up to fabricate patch pipettes that seal on virtually any membrane, yielding low access resistance and efficient intracellular perfusion.

Authors:  Mascia Benedusi; Marco Aquila; Alberto Milani; Giorgio Rispoli
Journal:  Eur Biophys J       Date:  2011-07-15       Impact factor: 1.733

3.  Ionic transport in lipid bilayer membranes.

Authors:  F Bordi; C Cametti; A Naglieri
Journal:  Biophys J       Date:  1998-03       Impact factor: 4.033

4.  Activation of the archaeal ion channel MthK is exquisitely regulated by temperature.

Authors:  Yihao Jiang; Vinay Idikuda; Sandipan Chowdhury; Baron Chanda
Journal:  Elife       Date:  2020-12-04       Impact factor: 8.140

5.  Two classes of alamethicin transmembrane channels: molecular models from single-channel properties.

Authors:  D O Mak; W W Webb
Journal:  Biophys J       Date:  1995-12       Impact factor: 4.033

6.  Multiple types of voltage-dependent Ca2+-activated K+ channels of large conductance in rat brain synaptosomal membranes.

Authors:  J Farley; B Rudy
Journal:  Biophys J       Date:  1988-06       Impact factor: 4.033

7.  Characterizing the membrane-bound state of cytochrome P450 3A4: structure, depth of insertion, and orientation.

Authors:  Javier L Baylon; Ivan L Lenov; Stephen G Sligar; Emad Tajkhorshid
Journal:  J Am Chem Soc       Date:  2013-05-30       Impact factor: 15.419

  7 in total

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