Neutron Spin Echo Spectroscopy Research Articles

An Alternative Explanation of the Microscopic Dynamics of Cyclic Polymers

AbstractAccording to recent reviews and experiments, some key dynamic properties of cyclic polymers from neutron spin echo spectroscopy, molecular dynamics simulations, and rheological measurements are at variance with the predictions from theories based on motions restricted by fixed obstacles. These dynamic properties including non‐Gaussianity, heterogeneity, and subdiffusive center of mass mean square displacements turn out to be hallmarks of cooperative dynamics found in entangled linear polymers, and in other many‐units interacting systems that are not polymers. The current situation suggests new theory emphasizing cooperative many‐chain dynamics is needed to explain the properties. The Coupling Model is such a theory. Its predictions are applied to the dynamic properties of cyclic polymers in this paper to show consistency with experiments and simulations.This article is protected by copyright. All rights reserved

Activation energy and molecular weight dependence of cooperative tracer chains diffusion in highly entangled polymer melts

AbstractThe generalized Langevin equation for cooperative dynamics of Guenza predicts the dynamics of chains in entangled polymers is cooperative with anomalous properties, and at variance with the tube‐reptation model. The center‐of‐mass mean‐square displacements at shorter times are subdiffusive with with β < 1, contradicting the common assumption of reptation within the tube. At some longer time the subdiffusive dynamics exhibits the crossover to free diffusion with . Moreover the subdiffusive dynamics is heterogeneous, non‐Gaussian, and cooperative. These predictions have been confirmed by using neutron spin echo spectroscopy in entangled polyethylene melts [M. Zamponi, et al. J. Phys. Chem. B 2008, 112, 16220], and in tracer diffusion of short polyethylene chains in a highly entangled polyethylene melt [M. Zamponi et al. Phys. Rev. Lett. 2021, 126, 187801]. The latter was confirmed in poly(ethylene oxide) tracer diffusion in highly entangled poly(ethylene oxide) melt [M. Kruteva et al. Macromolecules 2021, 54, 11384]. Notwithstanding, there are other important data sets obtained in the NSE experiments but were left unexplained. One set consists of the activation energies of the Arrhenius temperature dependence of D for each tracer. Another is the molecular weight dependence of D of the tracers determined at the same temperature. In this article the predictions of the Coupling Model are applied to these two sets of data. Good quantitative agreements of the CM predictions with experimental data provide additional support to the cooperativity dynamics of entangled polymers as concluded by others. Additionally, all the properties of cooperative diffusion of entangled polymer chains are shown to be isomorphic to those found in cooperative diffusions in totally different systems. Diffusion in all are governed by interaction between the diffusing units, and from which the universal properties originate.

Antivesiculation and Complete Unbinding of Tail-Tethered Lipids.

We report the effect of tail-tethering on vesiculation and complete unbinding of bilayered membranes. Amphiphilic molecules of a bolalipid, resembling the tail-tethered molecular structure of archaeal lipids, with two identical zwitterionic phosphatidylcholine headgroups self-assemble into a large flat lamellar membrane, in contrast to the multilamellar vesicles (MLVs) observed in its counterpart, monopolar nontethered zwitterionic lipids. The antivesiculation is confirmed by small-angle X-ray scattering (SAXS) and cryogenic transmission electron microscopy (cyro-TEM). With the net charge of zero and higher bending rigidity of the membrane (confirmed by neutron spin echo (NSE) spectroscopy), the current membrane theory would predict that membranes should stack with each other (aka "bind") due to dominant van der Waals attraction, while the outcome of the nonstacking ("unbinding") membrane suggests that the theory needs to include entropic contribution for the nonvesicular structures. This report pioneers an understanding of how the tail-tethering of amphiphiles affects the structure, enabling better control over the final nanoscale morphology.

Introduction to neutron scattering

Neutron scattering is a very high-performance method for studying the structure and dynamics of condensed matter with similar approaches in wide ranges of space and time, matching dimensions in space from single atoms to macromolecules and in time from atomic vibrations over crystal phonons to low-lying transitions in the microwave range, and to motions of large molecular units. Concerning the number and depth of physical concepts, neutron scattering may be compared to modern nuclear magnetic resonance. Neutrons have contributed essential results to the understanding of atomic and molecular processes and are, in this respect, complementary to other materials science probes. Among others, three properties of thermal neutrons make them especially appropriate for such work: the neutron mass is similar to atomic masses, and both neutron energies and the wavelengths of the neutron material wave match typical values for condensed matter. A further important feature of neutron scattering, making it especially valuable in biochemistry and polymer sciences, is that hydrogen and deuterium atoms very significantly and specifically contribute to the signal in both diffraction and spectroscopy. Additionally, neutrons are scattered at the nuclei and directly reflect the nuclear structure and motions. Results from neutron scattering are of great general interest. This paper aims to provide an introduction for chemists on a level understandable also to students and researchers who are not going to become part of the neutron community and will not be involved in the experiments, but shall be able to understand the basic concepts of the method and its relevance to modern chemistry. The paper focuses on basic theory, typical experiments, and some examples demonstrating the applications. As for many modern experimental techniques, the interpretation of the results of neutron scattering is based on theoretical models and requires a significant mathematical overhead. Most results are only meaningful when compared with computer simulations. For understanding this, in this paper, the theory of scattering is developed, starting with intuitive models and presenting typical concepts such as the scattering triangle, energy and momentum transfer, and the relation of inelastic and elastic scattering to space- and time-dependent information. The interaction of neutrons with matter, scattering cross sections, beam attenuation, and coherent versus incoherent scattering are explained in detail. Two further typical concepts that are not generally familiar to scientists outside the community are the use of wave and particle equivalence, and of handling results as a scattering function that depends simultaneously on momentum and energy transfers. The possibility of obtaining neutron beams for scattering experiments at a few research centers around high-performance sources is explained, and experimentally relevant features of research reactors and spallation sources are mentioned. As neutron experiments always have to deal with small flux and extended beams and shielding, experimental conditions are very far away from laboratory methods where handling of samples and instruments is concerned. Experimental details are given for making experiments more understandable and familiarizing the reader with the method. Related to this are extended possibilities for handling samples in a large variety of different environments. In a further part of the manuscript, a variety of techniques and typical instruments are presented, together with some characteristic applications bringing alive the theory developed so far. This covers powder diffraction and structure of liquid water, triple-axis spectrometers and lattice phonons, backscattering spectrometry and rotational tunneling, time-of-flight spectrometry, and simultaneously probing the energy and shape of low lying vibrations and diffusion, filter spectrometer and vibrational spectroscopy without selection rules, small-angle neutron scattering and protein unfolding, as well as micelles, neutron spin echo spectroscopy, and polymer dynamics.

Interchain Hydrodynamic Interaction and Internal Friction of Polyelectrolytes.

Polyelectrolytes (PE) are polymeric macromolecules in aqueous solutions characterized by their chain topology and intrinsic charge in a neutralizing fluid. Structure and dynamics are related to several characteristic screening length scales determined by electrostatic, excluded volume, and hydrodynamic interactions. We examine PE dynamics in dilute to semidilute conditions using dynamic light scattering, neutron spinecho spectroscopy, and pulse field gradient NMR spectroscopy. We connect macroscopic diffusion to segmental chain dynamics, revealing a decoupling of local chain dynamics from interchain interactions. Collective diffusion is described within a colloidal picture, including electrostatic and hydrodynamic interactions. Chain dynamics is characterized by the classical Zimm model of a neutral chain retarded by internal friction. We observe that hydrodynamic interactions are not fully screened between chains and that the internal friction within the chain increases with an increase in ion condensation on the chain.

Persistent dynamic magnetic state in artificial honeycomb spin ice

Topological magnetic charges, arising due to the non-vanishing magnetic flux on spin ice vertices, serve as the origin of magnetic monopoles that traverse the underlying lattice effortlessly. Unlike spin ice materials of atomic origin, the dynamic state in artificial honeycomb spin ice is conventionally described in terms of finite size domain wall kinetics that require magnetic field or current application. Contrary to this common understanding, here we show that a thermally tunable artificial permalloy honeycomb lattice exhibits a perpetual dynamic state due to self-propelled magnetic charge defect relaxation in the absence of any external tuning agent. Quantitative investigation of magnetic charge defect dynamics using neutron spin echo spectroscopy reveals sub-ns relaxation times that are comparable to the relaxation of monopoles in bulk spin ices. Most importantly, the kinetic process remains unabated at low temperature where thermal fluctuation is negligible. This suggests that dynamic phenomena in honeycomb spin ice are mediated by quasi-particle type entities, also confirmed by dynamic Monte-Carlo simulations that replicate the kinetic behavior. Our research unveils a macroscopic magnetic particle that shares many known traits of quantum particles, namely magnetic monopole and magnon.

Neutron spin echo spectroscopy with a moving sample

Neutron spin echo spectroscopy is a high resolution inelastic neutron scattering method probing nanosecond dynamics. It is well suited to study the atomistic motion in polymer systems and contributes to our understanding of viscoelasticity. However, for samples under shear, or moving samples in general, Doppler scattering has to be considered. We compare the measured phase shift and depolarisation due to Doppler scattering from a rotating graphite disk to numerical and analytical calculations and find excellent agreement. This allows to take into account Doppler scattering during the data processing and makes longer Fourier times as well as higher shear rates and Q ranges possible with neutron spin echo spectroscopy, enabling for example the study of polymers under high shear.

Hindered segmental dynamics in associative protein hydrogels studied by neutron spin-echo spectroscopy

Hindered segmental dynamics in associative protein hydrogels studied by neutron spin-echo spectroscopy

End block dynamics in unentangled polymers by dielectric spectroscopy

Dielectric spectroscopy measures the dynamics of polymer melts over a broad frequency range. Developing a theory for the spectral shape can extend the analysis of dielectric spectra beyond determining relaxation times from the peak maxima and adds physical meaning to shape parameters determined with empirical fit functions. Toward this goal, we use the experimental results on unentangled poly(isoprene), and unentangled poly(butylene oxide), polymer melts, to test whether the concept of end blocks could be one reason for the Rouse model deviating from experimental data. These end blocks have been suggested by simulations and neutron spin echo spectroscopy and are a consequence of the monomeric friction coefficient depending on the position of the bead in the chain. The concept of an end block is an approximation which partitions the chain in a middle and two end blocks to avoid overparameterization by a continuous position dependent change of the friction parameter. Analysis of dielectric spectra shows that the deviations of the calculated from the experimental normal mode cannot be related to the end block relaxation. However, the results do not contradict an end block hiding below the segmental relaxation peak. It seems that the results are compatible with an end block being the specific part of the sub-Rouse chain interpretation close to the chain ends.

Integrative dynamic structural biology unveils conformers essential for the oligomerization of a large GTPase.

Guanylate binding proteins (GBPs) are soluble dynamin-like proteins that undergo a conformational transition for GTP-controlled oligomerization and disrupt membranes of intracellular parasites to exert their function as part of the innate immune system of mammalian cells. We apply neutron spin echo, X-ray scattering, fluorescence, and EPR spectroscopy as techniques for integrative dynamic structural biology to study the structural basis and mechanism of conformational transitions in the human GBP1 (hGBP1). We mapped hGBP1's essential dynamics from nanoseconds to milliseconds by motional spectra of sub-domains. We find a GTP-independent flexibility of the C-terminal effector domain in the µs-regime and resolve structures of two distinct conformers essential for an opening of hGBP1 like a pocket knife and for oligomerization. Our results on hGBP1's conformational heterogeneity and dynamics (intrinsic flexibility) deepen our molecular understanding relevant for its reversible oligomerization, GTP-triggered association of the GTPase-domains and assembly-dependent GTP-hydrolysis.

Impact of transmembrane peptides on individual lipid motions and collective dynamics of lipid bilayers

The fluid nature of lipid bilayers is indispensable for the dynamic regulation of protein function and membrane morphology in biological membranes. Membrane-spanning domains of proteins interact with surrounding lipids and alter the physical properties of lipid bilayers. However, there is no comprehensive view of the effects of transmembrane proteins on the membrane's physical properties. Here, we investigated the effects of transmembrane peptides with different flip-flop-promoting abilities on the dynamics of a lipid bilayer employing complemental fluorescence and neutron scattering techniques. The quasi-elastic neutron scattering and fluorescence experiments revealed that lateral diffusion of the lipid molecules and the acyl chain motions were inhibited by the inclusion of transmembrane peptides. The neutron spin-echo spectroscopy measurements indicated that the lipid bilayer became more rigid but more compressible and the membrane viscosity increased when the transmembrane peptides were incorporated into the membrane. These results suggest that the inclusion of rigid transmembrane structures hinders individual and collective lipid motions by slowing down lipid diffusion and increasing interleaflet coupling. The present study provides a clue for understanding how the local interactions between lipids and proteins change the collective dynamics of the lipid bilayers, and therefore, the function of biological membranes.

Distributing aminophospholipids asymmetrically across leaflets causes anomalous membrane stiffening

We studied the mechanical leaflet coupling of prototypic mammalian plasma membranes using neutron spin-echo spectroscopy. In particular, we examined a series of asymmetric phospholipid vesicles with phosphatidylcholine and sphingomyelin enriched in the outer leaflet and inner leaflets composed of phosphatidylethanolamine/phosphatidylserine mixtures. The bending rigidities of most asymmetric membranes were anomalously high, exceeding even those of symmetric membranes formed from their cognate leaflets. Only asymmetric vesicles with outer leaflets enriched in sphingolipid displayed bending rigidities in conformity with these symmetric controls. We performed complementary small-angle neutron and x-ray experiments on the same vesicles to examine possible links to structural coupling mechanisms, which would show up in corresponding changes in membrane thickness. In addition, we estimated differential stress between leaflets originating either from a mismatch of their lateral areas or spontaneous curvatures. However, no correlation with asymmetry-induced membrane stiffening was observed. To reconcile our findings, we speculate that an asymmetric distribution of charged or H-bond forming lipids may induce an intraleaflet coupling, which increases the weight of hard undulatory modes of membrane fluctuations and hence the overall membrane stiffness.

Experimental critical dynamics of 3-methyl pyridine/D2O mixtures without and with antagonistic salt

We observed criticality in the structure and dynamics of a three-dimensional (3D) and two-dimensional (2D) Ising system consisting of 3-methyl pyridine $\text{(3MP)}/{\mathrm{D}}_{2}\mathrm{O}$ without and with antagonistic salt. We could describe both dynamic criticalities by the Kawasaki crossover function. The dynamic critical exponent was $z=0.063\ifmmode\pm\else\textpm\fi{}0.020$ and $0.005\ifmmode\pm\else\textpm\fi{}0.019$ for three and two dimensions, which confirms earlier observations in the 3D case and confirms expectations in the 2D case. The amplitudes of the critical dynamics are governed by the bare viscosities experimentally, and by the coefficient $R$ theoretically [the latter is proportional to ${(4\ensuremath{-}d)}^{\ensuremath{-}1}$ with the dimensionality $d$]. This finding is in accordance with the lubrication effect [N. Gov, A. G. Zilman, and S. Safran, Phys. Rev. E 70, 011104 (2004)], which is also connected to lamellar systems of the Brazovskii criticality [M. Gvaramia et al., Colloid Polym. Sci. 297, 1507 (2019)]. This lubrication effect is tightly connected to a laminar flow enforced by the domain structure, and it also holds for our 2D Ising system. The experimental techniques employed were small-angle neutron and x-rays scattering for the static criticality, and dynamic light scattering and neutron spin echo spectroscopy for the critical dynamics. Furthermore, the criticality of the viscosities was measured.

Dynamics of the extended and intermediate range order in model polymer electrolyte poly(ethylene oxide) and lithium bis(trifluoromethanesulfonyl)imide

The dynamics of lithium ions and polymer chains were investigated at the molecular scale in the model polymer electrolyte Poly (ethylene oxide) (PEO)/Lithium bis(trifluoromethanesulfonyl)imide as a function of temperature. This system is known to present an intermediate range order from the arrangement of neighboring chain segments as well as an extended range order of cylindrically arranged chains. The collective dynamics of the systems at lengthscales matching these structural features was measured using Neutron Spin Echo spectroscopy, gaining insights into their lifetime. Moreover, using isotope substitution techniques the dynamics of the lithium ions with respect to the other atoms was probed. The obtained results are compared with the conductivity and the lithium self-diffusion coefficient measured by NMR to gain experimental insight on the molecular processes triggering lithium transport.

Investigation of the Impact of Lipid Acyl Chain Saturation on Fusion Peptide Interactions with Lipid Bilayers

The interaction of many peptides with lipid bilayer membranes strongly depends on the lipid composition. Here, a study of the impact of unsaturated lipid acyl chains on the interaction of a derivative of the HIV-1 fusion peptide with lipid bilayer vesicles is presented. Lipid bilayer vesicles composed of mixtures of lipids with two saturated acyl chains and lipids and one saturated and one unsaturated acyl chain, but identical head groups, were studied. The dependence of the peptide conformation on the unsaturated lipid content was probed by circular dichroism spectroscopy, while the impact of the peptide on the bilayer structure was determined by small-angle neutron scattering. The impact of the peptide on the lipid bilayer vesicle dynamics was investigated using neutron spin echo spectroscopy. Molecular dynamics simulations were used to characterize the behavior of the systems studied to determine if there were clear differences in their physical properties. The results reveal that the peptide–bilayer interaction is not a simple function of the unsaturated lipid acyl chain content of the bilayer. Instead, the peptide behavior is more consistent with that seen for the bilayer containing only unsaturated lipids, which is supported by lipid-specific interactions revealed by the simulations.

Asymmetric distribution of aminophospholipids stiffens fluid membranes.

Cellular envelopes contain a large number of lipid species that distribute asymmetrically between the two leaflets of the bilayer. For example, mammalian plasma membranes are composed of an outer leaflet enriched in cholinephospholipids, while the majority of the aminophospholipids are confined to the inner leaflet. Membrane asymmetry can theoretically lead to distinct effects regarding its elastic behavior, either due to lipid specific properties (e.g. size, shape), or simply lipid over/under-crowding of a given leaflet. Corresponding experimental data are scarce. This prompted us to determine the structure and bending rigidity of minimal mammalian plasma membrane mimics composed of milk sphingomyelin (MSM), palmitoyl oleoyl phosphatidylcholine (POPC), palmitoyl oleoyl phosphatidylethanolamine (POPE), and palmitoyl oleoyl phosphatidylserine (POPS) using small-angle neutron/X-ray scattering and neutron spin echo spectroscopy. Most strikingly, we observed an anomalous stiffening of freely-floating fluid vesicles (size ∼ 100 nm) in case of inner leaflets composed of POPE/POPS mixtures and outer leaflets enriched in POPC. That is, the bending rigidities of POPCout/(POPE/POPS)in vesicles did not only exceed those of their scrambled (symmetric) analogs, but also those of symmetric vesicles mimicking either their inner and outer leaflets. Addition MSM in the outer leaflet reduced but not abolished this effect, possibly due to hydrocarbon chain interdigitation. To reconcile our findings, we speculate that lipid shape and charge asymmetry may increase the weight of short-wavelength undulatory modes in membranes by inducing a coupling at distances smaller than the membrane thickness.

The interdependence of thermodynamic, mechanical, and structural properties in saturated phospholipid membranes.

Lipid membranes undergo conformational and structural changes when they transition from the gel phase to the fluid phase. These phase transitions are accompanied by changes in the lipid packing and the membrane mechanical properties, as previously reported in experimental studies and molecular dynamics simulations. Here, we report a simple direct approach for calculating the mechanical properties of single-component lipid membranes using size-dependent calorimetry measurements, performed on lipid vesicles with different mean diameters. Using differential scanning calorimetry (DSC), we find that the melting temperature, associated with the gel-to-fluid phase transition, increases with the vesicle diameter until it approaches an asymptotic value representative of uncurved membranes. More importantly, fits of the transition temperature as a function of vesicle size show a clear dependence on the structural and mechanical properties of the membranes, i.e., the area-per-lipid and the area compressibility modulus. Our method is validated by comparing the obtained parameters against results from small-angle X-ray scattering measurements and Langmuir monolayer compression studies. The findings indicate that the thermodynamic properties of vesicular lipid membranes depend on their nanoscale curvature and corresponding energetic contributions for membrane stretching and bending. When combined with measurements of the bending rigidity modulus by neutron spin-echo spectroscopy, our approach yields the interleaflet coupling constant, a sought-after quantity describing the extent of interactions between the two membrane leaflets. The application of this approach to saturated phospholipid membranes with molecular additives (e.g., cholesterol) provides a platform to assess the resultant effects on interleaflet interactions.

Domain-induced dynamics in phase-separating lipid membranes.

Lipid membranes have a significant role in cells, not only defining the boundaries of cells and cell organelles but also playing an active role in cell functions, including the partitioning of proteins and the spatiotemporal regulation of signaling clusters. This is facilitated by the rich lipid diversity in cell membranes, which often results in unideal mixing and subsequent lipid phase-separation into lateral compositional heterogeneities or domains. Over the past few decades, structural measurements on such membranes have shed important light on the molecular mechanisms underlying domain formation. However, major information gaps still exist in our understanding of how domain formation affects the dynamics of lipid membranes, whether in the form of collective fluctuations or molecular motions. To address this outstanding question, we use neutron spectroscopy and molecular dynamics (MD) simulations that can selectively investigate the matrix dynamics in domain-forming membranes. Specifically, our studies are performed on binary mixtures of 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) and deuterated 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC). Experimental results, obtained by neutron spin-echo spectroscopy and neutron backscattering spectroscopy, show that the formation and growth of rigid DSPC domains causes an effective slowdown in the bending fluctuations and diffusional dynamics of the otherwise fluid DMPC matrix. MD simulations on cognate bilayers suggest that the measured changes in the matrix dynamics are mediated by interfacial DMPC lipids that experience constrained diffusional jumps and longer residence times at the domain boundaries. Our findings present striking evidence of dynamic coupling between lipid domains and their surrounding lipid environment. More importantly, this interplay occurs on the nanosecond time scales of protein conformational changes and signaling events. Put together, the results suggest an intriguing mechanism by which domain formation can play a regulatory role in functional membrane processes.

Investigating structure-property relations in cholesterol-rich lipid membranes.

Cholesterol is a key molecule in eukaryotic cell membranes. It mediates essential membrane processes, including viral budding and the mechanical resistance of membranes against pathogens. Hence, understanding the influence of cholesterol on the mechanics of functional membranes is crucial. Cholesterol is known to cause lipids to pack more tightly, manifesting in a decrease in the average area per lipid, AL, at the aqueous interface. Yet, how variations in packing density influence the elastic properties of lipid membranes with varying degrees of chain unsaturation remains largely unexplored. Theories based on mean field calculations have predicted various forms of the interdependence between the bending rigidity modulus, κ, and lipid packing density. However, direct assessments of these predictions have been limited, due to the difficulty in accessing the membrane's mechanical properties on the nanoscale. To address this, we performed studies using neutron spin-echo spectroscopy, solid-state 2H NMR relaxometry, and molecular dynamics simulations on lipid membranes with different degrees of chain unsaturation. We find that cholesterol has a stiffening effect on all studied membranes over the accessible length and time scales. Our findings show that κ has an inverse dependence on AL, indicating that cholesterol controls membrane elastic properties by modifying lipid packing density. As AL decreases, the number of conformations accessible to the lipid chains also decreases and the membrane becomes more rigid. Yet, different expressions of κ vs. AL are obtained when we consider reduced variables. Establishing well-defined structure-property relationships will open up new possibilities for predicting the behavior of more complex biological membranes and will inform design rules for engineered membranes and artificial cells with real-world functionalities.

Nanoscale membrane dynamics in chain asymmetric lipid bilayers.

Lipids that have two tails of different lengths are found throughout biomembranes in nature, yet the effects of this asymmetry on the membrane properties are not well understood, especially the membrane dynamics. Accommodating such a difference in tail length could significantly impact the membrane dynamics and elastic properties depending on how the longer tail is situated within the bilayer. To probe these effects, here we study the nanoscale bending fluctuations in model chain-asymmetric 14:0-18:0 PC (MSPC) and 18:0-14:0 PC (SMPC) lipid bilayers using neutron spin echo (NSE) spectroscopy. We find that despite the partial interdigitation that is known to persist in the fluid phase of these membranes, the collective fluctuations are enhanced on timescales of tens of nanoseconds, and the chain-asymmetric lipid bilayers are softer than an analogous chain-symmetric lipid with the same average number of carbons in the acyl tails, di-16:0 PC (DPPC). Quantitative comparison of the NSE results suggests that the enhanced bending fluctuations at the nanosecond timescales are consistent with experimental and computational studies that showed the compressibility moduli of chain-asymmetric lipid membranes are 20 % to 40% lower than chain-symmetric lipid membranes. These studies add to growing evidence that the partial interdigitation in chain-asymmetric lipid membranes in the fluid phase is highly dynamic and influences membrane dynamic processes from the molecular to mesoscopic length scales without significantly changing the bilayer thickness or area per lipid.