PMID- 9370456 OWN - NLM STAT- MEDLINE DCOM- 19980116 LR - 20220317 IS - 0006-3495 (Print) IS - 1542-0086 (Electronic) IS - 0006-3495 (Linking) VI - 73 IP - 5 DP - 1997 Nov TI - Exchange of monooleoylphosphatidylcholine as monomer and micelle with membranes containing poly(ethylene glycol)-lipid. PG - 2615-29 AB - Surface-grafted polymers, such as poly(ethylene glycol) (PEG), provide an effective steric barrier against surface-surface and surface-macromolecule interactions. In the present work, we have studied the exchange of monooleoylphosphatidylcholine (MOPC) with vesicle membranes containing 750 mol wt surface-grafted PEG (incorporated as PEG-lipid) from 0 to 20 mol % and have analyzed the experimental results in terms of thermodynamic and stationary equilibrium models. Micropipette manipulation was used to expose a single lipid vesicle to a flow of MOPC solution (0.025 microM to 500 microM). MOPC uptake was measured by a direct measure of the vesicle area change. The presence of PEG(750) lipid in the vesicle membrane inhibited the partitioning of MOPC micelles (and to some extent microaggregates) into the membrane, while even up to 20 mol % PEG-lipid, it did not affect the exchange of MOPC monomers both into and out of the membrane. The experimental data and theoretical models show that grafted PEG acts as a very effective molecular scale "filter" and prevents micelle-membrane contact, substantially decreasing the apparent rate and amount of MOPC taken up by the membrane, thereby stabilizing the membrane in a solution of MOPC that would otherwise dissolve it. FAU - Needham, D AU - Needham D AD - Department of Mechanical Engineering and Materials Science, Duke University, Durham, North Carolina 27708-0300, USA. FAU - Stoicheva, N AU - Stoicheva N FAU - Zhelev, D V AU - Zhelev DV LA - eng GR - GM 40162/GM/NIGMS NIH HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - Biophys J JT - Biophysical journal JID - 0370626 RN - 0 (Lipid Bilayers) RN - 0 (Liposomes) RN - 0 (Lysophosphatidylcholines) RN - 0 (Micelles) RN - 0 (Phosphatidylcholines) RN - 0 (Phosphatidylethanolamines) RN - 0 (Phospholipids) RN - 133906-05-5 (dioleoyl-N-(monomethoxypolyethylene glycol succinyl)phosphatidylethanolamine) RN - 3WJQ0SDW1A (Polyethylene Glycols) RN - 6753-56-6 (1-stearoyl-2-oleoyl-sn-glycero-3-phosphocholine) SB - IM MH - Kinetics MH - Lipid Bilayers/*chemistry/metabolism MH - Liposomes/chemistry/metabolism MH - Lysophosphatidylcholines/*chemistry/metabolism MH - Membrane Fusion MH - Micelles MH - Microscopy, Video MH - Models, Biological MH - Phosphatidylcholines/metabolism MH - Phosphatidylethanolamines/*chemistry/metabolism MH - Phospholipids/chemistry/metabolism MH - Polyethylene Glycols/*chemistry/metabolism MH - Surface Properties MH - Thermodynamics PMC - PMC1181164 EDAT- 1997/11/25 00:00 MHDA- 1997/11/25 00:01 PMCR- 1998/11/01 CRDT- 1997/11/25 00:00 PHST- 1997/11/25 00:00 [pubmed] PHST- 1997/11/25 00:01 [medline] PHST- 1997/11/25 00:00 [entrez] PHST- 1998/11/01 00:00 [pmc-release] AID - S0006-3495(97)78291-2 [pii] AID - 10.1016/S0006-3495(97)78291-2 [doi] PST - ppublish SO - Biophys J. 1997 Nov;73(5):2615-29. doi: 10.1016/S0006-3495(97)78291-2.