| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | John Sanderson | Q42873492 |
| P2860 | cites work | The Protein Data Bank | Q24515306 |
| MSI-78, an Analogue of the Magainin Antimicrobial Peptides, Disrupts Lipid Bilayer Structure via Positive Curvature Strain | Q24537642 | ||
| Specific roles of protein-phospholipid interactions in the yeast cytochrome bc1 complex structure | Q27636481 | ||
| The X-ray crystal structures of wild-type and EQ(I-286) mutant cytochrome c oxidases from Rhodobacter sphaeroides | Q27639427 | ||
| Interactions between lipids and bacterial reaction centers determined by protein crystallography | Q27639471 | ||
| Structure of the yeast cytochrome bc1 complex with a hydroxyquinone anion Qo site inhibitor bound | Q27641377 | ||
| BAR domains as sensors of membrane curvature: the amphiphysin BAR structure | Q27642663 | ||
| A voltage-gated ion channel model inferred from the crystal structure of alamethicin at 1.5-Å resolution | Q27729134 | ||
| Macromolecular structural elucidation with solid-state NMR-derived orientational constraints | Q27733428 | ||
| Structure of staphylococcal alpha-hemolysin, a heptameric transmembrane pore | Q27734044 | ||
| Antimicrobial peptides of multicellular organisms | Q28131811 | ||
| The fluid mosaic model of the structure of cell membranes | Q28239890 | ||
| Structure, location, and lipid perturbations of melittin at the membrane interface | Q28346294 | ||
| C2 domains from different Ca2+ signaling pathways display functional and mechanistic diversity | Q28360864 | ||
| Folding of beta-sheets in membranes: specificity and promiscuity in peptide model systems | Q30168121 | ||
| Amino acid distributions in integral membrane protein structures | Q30168203 | ||
| Folding of beta-sheet membrane proteins: a hydrophobic hexapeptide model | Q30176192 | ||
| Membrane fusion: a structural perspective on the interplay of lipids and proteins | Q30311181 | ||
| How membranes shape protein structure. | Q30328356 | ||
| The progress of membrane protein structure determination | Q30342003 | ||
| Staphylococcal alpha-hemolysin can form hexamers in phospholipid bilayers | Q30471871 | ||
| Phase equilibria of cholesterol/dipalmitoylphosphatidylcholine mixtures: 2H nuclear magnetic resonance and differential scanning calorimetry | Q30571359 | ||
| Orientation and dynamics of an antimicrobial peptide in the lipid bilayer by solid-state NMR spectroscopy | Q30660992 | ||
| Importance of hydration for gramicidin-induced hexagonal HII phase formation in dioleoylphosphatidylcholine model membranes | Q30688581 | ||
| Observing structure, function and assembly of single proteins by AFM. | Q30847493 | ||
| Observing single biomolecules at work with the atomic force microscope. | Q30913966 | ||
| The preference of tryptophan for membrane interfaces. | Q31997161 | ||
| Atomic force bio-analytics | Q33194255 | ||
| A review of enabling technologies based on scanning probe microscopy relevant to bioanalysis | Q33201846 | ||
| Lipid translocation across the plasma membrane of mammalian cells | Q33710622 | ||
| Common structural features in gramicidin and other ion channels | Q33843435 | ||
| Analysis of the PilQ secretin from Neisseria meningitidis by transmission electron microscopy reveals a dodecameric quaternary structure. | Q33996354 | ||
| Virulence functions of autotransporter proteins | Q34006158 | ||
| Customizing model membranes and samples for NMR spectroscopic studies of complex membrane proteins | Q34088688 | ||
| Regulation of transbilayer plasma membrane phospholipid asymmetry | Q34176163 | ||
| Mechanisms of antimicrobial peptide action and resistance | Q34181099 | ||
| Lipid-Gramicidin Interactions: Dynamic Structure of the Boundary Lipid by 2D-ELDOR | Q34181198 | ||
| Orientation and lipid-peptide interactions of gramicidin A in lipid membranes: polarized attenuated total reflection infrared spectroscopy and spin-label electron spin resonance | Q34184982 | ||
| Lipid distribution and transport across cellular membranes. | Q34211801 | ||
| Molecular modeling of the membrane targeting of phospholipase C pleckstrin homology domains | Q34224362 | ||
| Synthetic peptides that exert antimicrobial activities in whole blood and blood-derived matrices | Q34252687 | ||
| The role of caveolae and caveolin in vesicle-dependent and vesicle-independent trafficking | Q34365121 | ||
| beta-Peptides: from structure to function | Q34440559 | ||
| Non-haemolytic beta-amino-acid oligomers | Q34508218 | ||
| Advances in membrane receptor screening and analysis. | Q34649652 | ||
| Surface plasmon resonance spectroscopy: an emerging tool for the study of peptide-membrane interactions | Q34850080 | ||
| Lipid rafts: bringing order to chaos | Q35058353 | ||
| Attenuated total reflection IR spectroscopy as a tool to investigate the orientation and tertiary structure changes in fusion proteins | Q35182236 | ||
| Fusion peptides and the mechanism of viral fusion | Q35182242 | ||
| Lipid-peptide interaction in oriented bilayers probed by interface-sensitive scattering methods. | Q35209266 | ||
| Synthetic peptides as models for intrinsic membrane proteins | Q35590020 | ||
| New insights into water-phospholipid model membrane interactions | Q35780860 | ||
| Organization of G proteins and adenylyl cyclase at the plasma membrane | Q36945617 | ||
| Structure-activity analysis of buforin II, a histone H2A-derived antimicrobial peptide: the proline hinge is responsible for the cell-penetrating ability of buforin II. | Q37219123 | ||
| Lipid rafts, caveolae, caveolin-1, and entry by Chlamydiae into host cells | Q37869242 | ||
| Effect of trehalose and sucrose on the hydration and dipole potential of lipid bilayers | Q38313012 | ||
| Effects of the eukaryotic pore-forming cytolysin Equinatoxin II on lipid membranes and the role of sphingomyelin | Q40233583 | ||
| Effect of sodium chloride on a lipid bilayer | Q40251852 | ||
| The effects of gramicidin on the structure of phospholipid assemblies | Q40252072 | ||
| Tryptophan spectroscopy studies and black lipid bilayer analysis indicate that the oligomeric structure of Cry1Ab toxin from Bacillus thuringiensis is the membrane-insertion intermediate | Q42616566 | ||
| Analyses of circular dichroism spectra of membrane proteins. | Q43152633 | ||
| Light- and guanosine 5'-3-O-(thio)triphosphate-sensitive localization of a G protein and its effector on detergent-resistant membrane rafts in rod photoreceptor outer segments | Q43586300 | ||
| Protein chemistry at membrane interfaces: non-additivity of electrostatic and hydrophobic interactions | Q43633074 | ||
| Facilitated phosphatidylcholine flip-flop across erythrocyte membranes using low molecular weight synthetic translocases | Q43654032 | ||
| De novo design, synthesis, and characterization of antimicrobial beta-peptides | Q43692803 | ||
| Self-association of model transmembrane alpha-helices is modulated by lipid structure | Q43759608 | ||
| Kinetics and thermodynamics of annexin A1 binding to solid-supported membranes: a QCM study | Q44082130 | ||
| Exploring peptide membrane interaction using surface plasmon resonance: differentiation between pore formation versus membrane disruption by lytic peptides | Q44276478 | ||
| Interfacial anchor properties of tryptophan residues in transmembrane peptides can dominate over hydrophobic matching effects in peptide-lipid interactions | Q44430419 | ||
| Position-dependence of stabilizing polar interactions of asparagine in transmembrane helical bundles | Q44454162 | ||
| Exposure of Phosphatidylinositol Transfer Proteins to Sphingomyelin−Cholesterol Membranes Suggests Transient but Productive Interactions with Raft-Like, Liquid-Ordered Domains | Q44649933 | ||
| Optical-trapping Raman microscopy detection of single unilamellar lipid vesicles | Q44670438 | ||
| Lipid packing sensed by ArfGAP1 couples COPI coat disassembly to membrane bilayer curvature | Q44679419 | ||
| 'Boomerang'-like insertion of a fusogenic peptide in a lipid membrane revealed by solid-state 19F NMR. | Q44744029 | ||
| Roles of curvature and hydrophobic interstice energy in fusion: studies of lipid perturbant effects | Q44808522 | ||
| Energetics of pore formation induced by membrane active peptides | Q44808534 | ||
| Analysis of liposomal membrane composition using Raman tweezers. | Q44873145 | ||
| Interfacial folding and membrane insertion of a designed helical peptide | Q44889250 | ||
| Domain formation in phosphatidylcholine bilayers containing transmembrane peptides: specific effects of flanking residues | Q45711199 | ||
| Perturbation of the hydrophobic core of lipid bilayers by the human antimicrobial peptide LL-37. | Q47275919 | ||
| Characterization of diphtheria toxin's catalytic domain interaction with lipid membranes | Q47992961 | ||
| Phases and phase transitions of the phosphatidylcholines. | Q50162208 | ||
| Antimicrobial 14-helical beta-peptides: potent bilayer disrupting agents. | Q52558984 | ||
| The C-terminal domain of the Pseudomonas secretin XcpQ forms oligomeric rings with pore activity. | Q54068546 | ||
| Three-dimensional model of purple membrane obtained by electron microscopy | Q56672667 | ||
| The Peptide Antibiotic Clavanin A Interacts Strongly and Specifically with Lipid Bilayers | Q57188169 | ||
| Membranolytic selectivity of cystine-stabilized cyclic protegrins | Q57236398 | ||
| Cholesterol–phospholipid interactions, the liquid-ordered phase and lipid rafts in model and biological membranes | Q57360230 | ||
| Visualization of Highly Ordered Striated Domains Induced by Transmembrane Peptides in Supported Phosphatidylcholine Bilayers† | Q57364906 | ||
| Kinetics and Mechanism of the Lamellar to Gyroid Inverse Bicontinuous Cubic Phase Transition | Q57904391 | ||
| A Designed Non-Peptidic Receptor that Mimics the Phosphocholine Binding Site of the McPC603 Antibody | Q57962712 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 201-212 | |
| P577 | publication date | 2004-11-26 | |
| P1433 | published in | Organic and Biomolecular Chemistry | Q3355939 |
| P1476 | title | Peptide-lipid interactions: insights and perspectives | |
| P478 | volume | 3 |
| Q27014021 | Antimicrobial peptides: their role as infection-selective tracers for molecular imaging |
| Q43034707 | Antiplasmodial activity study of angiotensin II via Ala scan analogs |
| Q35063550 | Applications of biological pores in nanomedicine, sensing, and nanoelectronics |
| Q62042504 | Conformation and Interaction of ad,l-Alternating Peptide with a Bilayer Membrane: X-ray Reflectivity, CD, and FTIR Spectroscopy |
| Q24645921 | Connexin channels and phospholipids: association and modulation |
| Q37007318 | Contribution of the Tyr-1 in Plantaricin149a to disrupt phospholipid model membranes |
| Q40013760 | Evidences for the action mechanism of angiotensin II and its analogs on Plasmodium sporozoite membranes |
| Q57370506 | Flexible macromolecules attached to lipid bilayers: impact on fluidity, curvature, permeability and stability of the membranes |
| Q92928668 | Fluorescence Imaging of Disrupted Interfaces between Liquid-Ordered and Liquid-Disordered Domains by a Flavin-Labeled PNA Duplex |
| Q40813580 | Fusion peptide P15-CSP shows antibiofilm activity and pro-osteogenic activity when deposited as a coating on hydrophilic but not hydrophobic surfaces |
| Q42216458 | Highly potential antiplasmodial restricted peptides |
| Q41411203 | Improved model systems for bacterial membranes from differing species: the importance of varying composition in PE/PG/cardiolipin ternary mixtures. |
| Q40631310 | Isoeugenol has a non-disruptive detergent-like mechanism of action |
| Q43233890 | LyeTx I, a potent antimicrobial peptide from the venom of the spider Lycosa erythrognatha |
| Q48158599 | Membrane binding and perturbation studies of the antimicrobial peptides caerin, citropin, and maculatin |
| Q40119866 | Noncovalent keystone interactions controlling biomembrane structure |
| Q50897095 | Novel antimicrobial peptide dendrimers with amphiphilic surface and their interactions with phospholipids--insights from mass spectrometry. |
| Q41847532 | Peptide adsorption to lipid bilayers: slow processes revealed by linear dichroism spectroscopy |
| Q28382825 | Peptide-Like Molecules (PLMs): A Journey from Peptide Bond Isosteres to Gramicidin S Mimetics and Mitochondrial Targeting Agents |
| Q44257735 | Permeabilization of baker's yeast with N-lauroyl sarcosine |
| Q24656426 | Surface features of a Mononegavirales matrix protein indicate sites of membrane interaction |
| Q57903111 | Synthetic pores with sticky π-clamps |
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