Volume enlargement and recovery of Na+-dependent amino acid transport in proteoliposomes derived from Ehrlich ascites cell membranes
- PMID: 3372516
Volume enlargement and recovery of Na+-dependent amino acid transport in proteoliposomes derived from Ehrlich ascites cell membranes
Abstract
Na+-dependent amino acid transport can be reconstituted from solubilized Ehrlich cell plasma membranes by addition of asolectin vesicles, gel filtration, and a freeze-thaw cycle. Removal of phosphatidic acid (approximately 10% of the total lipid) by Ba2+ precipitation reduces the efficiency of reconstitution of Na+-dependent amino acid transport by approximately 73% and decreases intravesicular volume of the proteoliposomes by approximately 43%. The loss of transport activity is not due to exclusion of specific proteins during reconstitution. The phosphatidic acid-free liposomes are less permeable and require more time to attain an equilibrium distribution of solute. Transport activity and intravesicular volume can be restored to Ba2+-precipitated asolectin proteoliposomes by addition of egg-phosphatidic acid during reconstitution. The extent of recovery of transport activity is proportional to the change in intravesicular volume and depends on the amount of phosphatidic acid present. Replacement of phosphatidic acid with 20% phosphatidylserine or phosphatidylglycerol leads to increases in intravesicular volume with little or no increase in amino acid transport. Generation of phosphatidic acid in situ by treatment of Ba2+-precipitated proteoliposomes with phospholipase D also restored transport. The observed increase in transport activity (9-fold) is accompanied by a 46% increase in intravesicular volume, presumably caused by vesicle fusion. Phosphatidic acid is also required for successful reconstitution of Na+-dependent amino acid transport from pure phosphatidylcholine:phosphatidylethanolamine (1:1) mixtures with only a small change (approximately 16%) in intravesicular volume. The results provide evidence for both indirect and direct effects of phosphatidic acid on reconstitution of Na+-dependent amino acid transport. The indirect effects occur through enlargement of intravesicular volume, large vesicles showing higher rates of transport. However, there is also evidence to indicate a specific effect of phosphatidic acid on the Na+-dependent amino acid transporter, since other acidic lipids may change intravesicular volume without a commensurate change in transport activity.
Similar articles
-
Role of specific acidic lipids on the reconstitution of Na(+)-dependent amino acid transport in proteoliposomes derived from Ehrlich cell plasma membranes.Biochemistry. 1990 May 15;29(19):4575-81. doi: 10.1021/bi00471a011. Biochemistry. 1990. PMID: 2372542
-
Effect of alkali cations on freeze-thaw-dependent reconstitution of amino acid transport from Ehrlich ascites cell plasma membrane.J Biol Chem. 1985 May 10;260(9):5706-14. J Biol Chem. 1985. PMID: 3988770
-
Asymmetric reconstitution of the glucose transporter from Ehrlich ascites cell plasma membrane: role of alkali cations.Arch Biochem Biophys. 1986 Jul;248(1):379-89. doi: 10.1016/0003-9861(86)90434-0. Arch Biochem Biophys. 1986. PMID: 3729423
-
The use of membrane vesicles in transport studies.CRC Crit Rev Biochem. 1980 Jan;7(3):187-246. doi: 10.3109/10409238009105462. CRC Crit Rev Biochem. 1980. PMID: 6243082 Review.
-
Proteoliposomes in nanobiotechnology.Biophys Rev. 2012 Mar;4(1):67-81. doi: 10.1007/s12551-011-0065-4. Epub 2012 Jan 18. Biophys Rev. 2012. PMID: 28510001 Free PMC article. Review.
Cited by
-
Identification of the integrin alpha 3 beta 1 as a component of a partially purified A-system amino acid transporter from Ehrlich cell plasma membranes.Biochem J. 1995 Nov 1;311 ( Pt 3)(Pt 3):743-51. doi: 10.1042/bj3110743. Biochem J. 1995. PMID: 7487928 Free PMC article.
-
Aggregatibacter actinomycetemcomitans leukotoxin cytotoxicity occurs through bilayer destabilization.Cell Microbiol. 2012 Jun;14(6):869-81. doi: 10.1111/j.1462-5822.2012.01762.x. Epub 2012 Mar 28. Cell Microbiol. 2012. PMID: 22309134 Free PMC article.
-
Competing Lipid-Protein and Protein-Protein Interactions Determine Clustering and Gating Patterns in the Potassium Channel from Streptomyces lividans (KcsA).J Biol Chem. 2015 Oct 16;290(42):25745-55. doi: 10.1074/jbc.M115.669598. Epub 2015 Sep 2. J Biol Chem. 2015. PMID: 26336105 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources