about
Phosphatidylinositol 4,5-bisphosphate clusters act as molecular beacons for vesicle recruitmentInteraction of calmodulin with Sec61α limits Ca2+ leakage from the endoplasmic reticulum.Multi-protein assemblies underlie the mesoscale organization of the plasma membrane.STED microscopy detects and quantifies liquid phase separation in lipid membranes using a new far-red emitting fluorescent phosphoglycerolipid analogue.Hydrophobic mismatch sorts SNARE proteins into distinct membrane domains.STED-FLCS: An Advanced Tool to Reveal Spatiotemporal Heterogeneity of Molecular Membrane DynamicsCalcium Promotes the Formation of Syntaxin 1 Mesoscale Domains through Phosphatidylinositol 4,5-Bisphosphate.A lipid bound actin meshwork organizes liquid phase separation in model membranesReorganization of Lipid Diffusion by Myelin Basic Protein as Revealed by STED Nanoscopy.Closing the gap: The approach of optical and computational microscopy to uncover biomembrane organization.GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane.Scanning STED-FCS reveals spatiotemporal heterogeneity of lipid interaction in the plasma membrane of living cells.Compartmentalization of the Cell Membrane.A near-infrared fluorophore for live-cell super-resolution microscopy of cellular proteins.Characterization of horizontal lipid bilayers as a model system to study lipid phase separation.A comparative study on fluorescent cholesterol analogs as versatile cellular reportersMembrane orientation and lateral diffusion of BODIPY-cholesterol as a function of probe structure.Coaligned dual-channel STED nanoscopy and molecular diffusion analysis at 20 nm resolution.Partitioning, diffusion, and ligand binding of raft lipid analogs in model and cellular plasma membranes.A high resolution electro-optical approach for investigating transition of soluble proteins to integral membrane proteins probed by colicin A.The 2015 super-resolution microscopy roadmapProtein conducting nanoporesPartitioning, Diffusion, and Ligand Binding of Raft Lipid Analogs in Model and Cellular Plasma MembranesFCS in STED MicroscopygSTED Microscopy with an OPSL: Cutting Edge Super-ResolutionExploring single-molecule dynamics with fluorescence nanoscopyA pathway for protons in nitric oxide reductase from Paracoccus denitrificansPhase separation provides a mechanism to reduce noise in cells
P50
Q27678096-DC52996B-7CCE-489C-A4E7-FA44BE99B77CQ28577802-9FA40EC1-A2F2-4FE0-ABB9-A169296646D9Q34014673-3E7CCE12-CC1F-4942-9FB4-CED203A98586Q34785818-6C66FA05-C0E2-4989-8BD4-2542314267CDQ35037311-C2488155-3DF5-4936-974C-618C9739DD3EQ35733868-2C450E1A-71EA-4E3F-BBBE-F1CC26EA2B38Q36778750-F82BB3FD-0B34-4543-9A9B-270498DC99B8Q37643178-6CCC33D2-29C2-43A7-A88A-311F6EA41D59Q38765892-DE233925-E650-4F47-8D39-4E1982679660Q38796634-7FD10ED1-B280-44D7-80C1-2C41C03943A3Q38883965-12A21D54-8EA8-444C-95A4-B0BBB5721740Q38939182-0624542B-4313-4242-9BE5-0C605BF175FEQ38976512-7314940F-B51A-4C41-93D9-AE7B7F450007Q39205820-4D7F9A28-1B79-4F18-9B88-22C3191CED9AQ41005471-BE5B824F-8A32-498C-B8CC-04CD527F1F40Q42013607-BF4A6FDF-567F-4D9E-B681-144EE4D9FD12Q42108783-6478E3BF-011C-47AD-AAF7-B06DF92EED0EQ43108066-1A2CB2A3-D9F3-47CE-859C-5247A92078FFQ52623579-93121D71-7D78-4DD9-8FB3-5EAF0021C6DCQ54327324-DC317BD2-767F-44B7-94AF-18ACD5C2F308Q56806459-A045547D-7F13-482C-BB91-1911115D0DBBQ57786538-F2C94764-8FC2-4D27-99AC-D8BE6B8EEE0AQ59286059-B8150F1F-0337-4FEA-9EFC-7E7C3EC69140Q63546513-97FA183D-DA98-4AAE-B4A3-8643B51B1588Q63546514-B8EB0D8F-12D8-497E-BF94-C9A857A93C77Q63546515-8E05B86E-8F85-41C2-AA54-FD292BEF0E67Q63546516-EAA9BB5E-C83E-4809-BA82-EB4EA697BA6CQ92889325-16D41BBF-437C-42CF-BF66-CE07CE5F3FD7
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Alf Honigmann
@ast
Alf Honigmann
@en
Alf Honigmann
@es
type
label
Alf Honigmann
@ast
Alf Honigmann
@en
Alf Honigmann
@es
prefLabel
Alf Honigmann
@ast
Alf Honigmann
@en
Alf Honigmann
@es
P1053
C-4832-2017
P106
P108
P21
P31
P3829
P496
0000-0003-0475-3790