Application Of Electron Paramagnetic Resonance Research Articles

Exploring the dynamics and structure of PpiB in living Escherichiacoli cells using electron paramagnetic resonance spectroscopy.

The combined effects of the cellular environment on proteins led to the definition of a fifth level of protein structural organization termed quinary structure. To explore the implication of potential quinary structure for globular proteins, we studied the dynamics and conformations of Escherichia coli (E. coli) peptidyl-prolyl cis/trans isomerase B (PpiB) in E. coli cells. PpiB plays a major role in maturation and regulation of folded proteins by catalyzing the cis/trans isomerization of the proline imidic peptide bond. We applied electron paramagnetic resonance (EPR) techniques, utilizing both Gadolinium (Gd(III)) and nitroxide spin labels. In addition to using standard spin labeling approaches with genetically engineered cysteines, we incorporated an unnatural amino acid to achieve Gd(III)-nitroxide orthogonal labeling. We probed PpiB's residue-specific dynamics by X-band continuous wave EPR at ambient temperatures and its structure by double electron-electron resonance (DEER) on frozen samples. PpiB was delivered to E. coli cells by electroporation. We report a significant decrease in the dynamics induced by the cellular environment for two chosen labeling positions. These changes could not be reproduced by adding crowding agents and cell extracts. Concomitantly, we report a broadening of the distance distribution in E. coli, determined by Gd(III)-Gd(III) DEER measurements, as compared with solution and human HeLa cells. This suggests an increase in the number of PpiB conformations present in E. coli cells, possibly due to interactions with other cell components, which also contributes to the reduction in mobility and suggests the presence of a quinary structure.

Magnetic Resonance-Based Analytical Tools to Study Polyvinylpyrrolidone-Hydroxyapatite Composites.

The synthesis of biocompatible and bioresorbable composite materials, such as a "polymer matrix-mineral constituent," stimulating the natural growth of living tissues and the restoration of damaged parts of the body, is one of the challenging problems in regenerative medicine and materials science. Composite films of bioresorbable polymer of polyvinylpyrrolidone (PVP) and hydroxyapatite (HA) were obtained. HA was synthesized in situ in the polymer solution. We applied electron paramagnetic resonance (EPR) and nuclear magnetic resonance (NMR) approaches to study the composite films' properties. The application of EPR in two frequency ranges allowed us to derive spectroscopic parameters of the nitrogen-based light and radiation-induced paramagnetic centers in HA, PVP and PVP-HA with high accuracy. It was shown that PVP did not significantly affect the EPR spectral and relaxation parameters of the radiation-induced paramagnetic centers in HA, while light-induced centers were detected only in PVP. Magic angle spinning (MAS) 1H NMR showed the presence of two signals at 4.7 ppm and -2.15 ppm, attributed to "free" water and hydroxyl groups, while the single line was attributed to 31P. NMR relaxation measurements for 1H and 31P showed that the relaxation decays were multicomponent processes that can be described by three components of the transverse relaxation times. The obtained results demonstrated that the applied magnetic resonance methods can be used for the quality control of PVP-HA composites and, potentially, for the development of analytical tools to follow the processes of sample treatment, resorption, and degradation.

Revealing the DNA Binding Modes of CsoR by EPR Spectroscopy.

In pathogens, a unique class of metalloregulator proteins, called gene regulatory proteins, sense specific metal ions that initiate gene transcription of proteins that export metal ions from the cell, thereby preventing toxicity and cell death. CsoR is a metalloregulator protein found in various bacterial systems that "sense" Cu(I) ions with high affinity. Upon copper binding, CsoR dissociates from the DNA promoter region, resulting in initiation of gene transcription. Crystal structures of CsoR in the presence and absence of Cu(I) from various bacterial systems have been reported, suggesting either a dimeric or tetrameric structure of these helical proteins. However, structural information about the CsoR-DNA complex is missing. Here, we applied electron paramagnetic resonance (EPR) spectroscopy to follow the conformational and dynamical changes that Mycobacterium tuberculosis CsoR undergoes upon DNA binding in solution. We showed that the quaternary structure is predominantly dimeric in solution, and only minor conformational and dynamical changes occur in the DNA bound state. Also, labeling of the unresolved C- terminus revealed no significant change in dynamics upon DNA binding. These observations are unique, since for other bacterial copper metalloregulators, such as the MerR and CopY families, major conformational changes were observed upon DNA binding, indicating a different mode of action for this protein family.

Electron paramagnetic resonance

We have studied literature from investigation of the impact of Mechanothermal effects in the creation of defect structures in dispersed systems after prolonged mechanical treatment of ZnO powders. This work illustrates some potential applications of electron paramagnetic resonance. EPR application beginning of a variety of paramagnetic processes is based on the knowledge that this centre happens when some materials are mechanically treated. These facilities can act as EPR sondes of various thermal processes that appear when systems are being mechanically treated consisting of ZnO.Zn was evaporated in air, dry and humid argon flow, and dry and humid nitrogen flow to create Zno tetrapod nanostructures. SEM, X-ray diffraction, photoluminescence, photoluminescence excitation (PLE) spectroscopy (at various temperatures), and electron paramagnetic resonance (EPR) spectroscopy at −160 ℃ and room temperature have all been used to explore the characteristics. It is discovered that the fabrication conditions have a considerable impact on the acquired EPR and PL spectra. while some of the samples exhibit a g = 1.96 EPR signal. We used microwave processing to create and mix ZnO nanoparticles (ZnO-NPs) with various amounts of graphene oxide (GO) (10 %, 20 %, and 30 %).The process delivered evenly distributed ZnO-NPs onto and between the rGO layers.(GZCs). The UV–vis absorption, PL emission, defect states of the ZnO, EPR signals, photo-electrochemical reaction, and charge transfer properties were all influenced by the annealing temperature and graphene oxide content. The GZCs' HRTEM microscopy pictures revealed interpenetrating structures and vacancy flaws that were easily seen. The findings showed that following hybridization with GO, the defect sites (Zn interstitials, oxygen vacancy, ionised oxygen vacancy, and oxygen interstitials) greatly decreased. The GZC-10photo-conversion 10 %'s efficiency(ŋ= 13.1 × 10-3%) We have studied literature from Ref.[1]which show that.

Application of Electron Paramagnetic Resonance in an Electrochemical Energy Storage System

The improvement of our living standards puts forward higher requirements for energy storage systems, especially rechargeable batteries. Unfortunately, phenomena such as capacity failure, etc. have been major difficulties in the field of energy storage. Therefore, we need some advanced means to explore the reaction process and mechanisms of the cell. Electron paramagnetic resonance (EPR) has the advantages of a high sensitivity to electrons, lack of damage to samples, quantitative analysis, etc., which can make for a more in-depth exploration of most paramagnetic electrode materials and metal electrode materials. After a brief description of the principle of EPR, this review briefly summarizes the application of EPR to the characterization of transition metal oxide cathode and lithium metal anode electrode materials in recent years, such as showing how to study electrode materials by using EPR in situ and operando .

X-Band Parallel-Mode and Multifrequency Electron Paramagnetic Resonance Spectroscopy of S = 1/2 Bismuth Centers.

The recent successes in the isolation and characterization of several bismuth radicals inspire the development of new spectroscopic approaches for the in-depth analysis of their electronic structure. Electron paramagnetic resonance (EPR) spectroscopy is a powerful tool for the characterization of main group radicals. However, the large electron–nuclear hyperfine interactions of Bi (209Bi, I = 9/2) have presented difficult challenges to fully interpret the spectral properties for some of these radicals. Parallel-mode EPR (B1∥B0) is almost exclusively employed for the study of S > 1/2 systems but becomes feasible for S = 1/2 systems with large hyperfine couplings, offering a distinct EPR spectroscopic approach. Herein, we demonstrate the application of conventional X-band parallel-mode EPR for S = 1/2, I = 9/2 spin systems: Bi-doped crystalline silicon (Si:Bi) and the molecular Bi radicals [L(X)Ga]2Bi• (X = Cl or I) and [L(Cl)GaBi(MecAAC)]•+ (L = HC[MeCN(2,6-iPr2C6H3)]2). In combination with multifrequency perpendicular-mode EPR (X-, Q-, and W-band frequencies), we were able to fully refine both the anisotropic g- and A-tensors of these molecular radicals. The parallel-mode EPR experiments demonstrated and discussed here have the potential to enable the characterization of other S = 1/2 systems with large hyperfine couplings, which is often challenging by conventional perpendicular-mode EPR techniques. Considerations pertaining to the choice of microwave frequency are discussed for relevant spin-systems.

Characterization of radicals in polysorbate 80 using electron paramagnetic resonance (EPR) spectroscopy and spin trapping

Polysorbates are an important class of nonionic surfactants that are widely used to stabilize biopharmaceuticals. The degradation of polysorbate 20 and 80 and the related particle formation in biologics are heavily discussed in the pharmaceutical community. Although a lot of experimental effort was spent in the detailed study of potential degradation pathways, the underlying mechanisms are only sparsely understood. Besides enzymatic hydrolysis, another proposed mechanism is associated with radical-induced (auto)oxidation of polysorbates. To characterize the types and the origin of the involved radicals and their propagation in bulk material as well as in diluted polysorbate 80 solutions, we applied electron paramagnetic resonance (EPR) spectroscopy using a spin trapping approach. The prerequisite for a meaningful experiment using spin traps is an understanding of the trapping rate, which is an interplay of (i) the presence of the spin trap at the scene of action, (ii) the specific reactivity of the selected spin trap with a certain radical as well as (iii) the stability of the formed spin adducts (a slow decay rate). We discuss whether and to which extent these criteria are fulfilled regarding the identification of different radical classes that might be involved in polysorbate oxidative degradation processes. The ratio of different radicals for different scenarios was determined for various polysorbate 80 quality grades in bulk material and in aqueous solution, showing differences in the ratio of present radicals. Possible correlations between the radical content and product parameters such as the quality grade, the manufacturing date, the manufacturer, the initial peroxide content according to the certificate of analysis of polysorbate 80 are discussed.

Maximizing the applicability of continuous wave (CW) Electron Paramagnetic Resonance (EPR): what more can we do after a century?

Electron Paramagnetic Resonance/Electron Spin Resonance (EPR/ESR) spectroscopy is a powerful experimental approach solving challenging problems that are inaccessible to other experimental techniques. While pulsed EPR techniques and their applications have been the central focus of the field nowadays, methodology development and application of continuous wave (CW) EPR have never been undervalued. Although the importance of EPR in research has been recognized in many areas as indicated by the increasing number of EPR research articles published every year, the growth in the number of EPR research teams seems to not match the former, likely caused by the relatively high cost of modern pulsed EPR spectrometers. In this perspective, we aim to discuss the new areas and new directions of the application of CW EPR in combination with spin labeling that are slightly different from the classic/traditional applications of the CW EPR technique. Based on our experience, we show example applications of CW EPR on the interfaces of protein-confinement materials, protein-inorganic crystal lattices, protein-nanoparticles, and protein-polymers. Various structure and dynamics information can be resolved from the data analysis of CW EPR, leading to enhanced understanding of protein biophysics upon interaction with the synthetic nanostructures as well as possible guidance of hybrid materials development based on the combination of proteins and nanostructures. We also discussed the possibilities of even broadening the application spectrum of EPR spectroscopy. The relatively high affordability of CW EPR spectrometers (as compared to the pulsed ones) also facilitates the growth in EPR research groups worldwide.

Probing Small-Angle Molecular Motions with EPR Spectroscopy: Dynamical Transition and Molecular Packing in Disordered Solids

Disordered molecular solids present a rather broad class of substances of different origin—amorphous polymers, materials for photonics and optoelectronics, amorphous pharmaceutics, simple molecular glass formers, and others. Frozen biological media in many respects also may be referred to this class. Theoretical description of dynamics and structure of disordered solids still does not exist, and only some phenomenological models can be developed to explain results of particular experiments. Among different experimental approaches, electron paramagnetic resonance (EPR) applied to spin probes and labels also can deliver useful information. EPR allows probing small-angle orientational molecular motions (molecular librations), which intrinsically are inherent to all molecular solids. EPR is employed in its conventional continuous wave (CW) and pulsed—electron spin echo (ESE)—versions. CW EPR spectra are sensitive to dynamical librations of molecules while ESE probes stochastic molecular librations. In this review, different manifestations of small-angle motions in EPR of spin probes and labels are discussed. It is shown that CW-EPR-detected dynamical librations provide information on dynamical transition in these media, similar to that explored with neutron scattering, and ESE-detected stochastic librations allow elucidating some features of nanoscale molecular packing. The possible EPR applications are analyzed for gel-phase lipid bilayers, for biological membranes interacting with proteins, peptides and cryoprotectants, for supercooled ionic liquids (ILs) and supercooled deep eutectic solvents (DESs), for globular proteins and intrinsically disordered proteins (IDPs), and for some other molecular solids.

Accurate measurement of atomic magnetic moments by minimizing the tip magnetic field in STM-based electron paramagnetic resonance

Electron paramagnetic resonance (EPR) performed with a scanning tunneling microscope (STM) allows for probing the spin excitation of single atomic species with MHz energy resolution. One of the basic applications of conventional EPR is the precise determination of magnetic moments. However, in an STM, the local magnetic fields of the spin-polarized tip can introduce systematic errors in the measurement of the magnetic moments by EPR. We propose to solve this issue by finding tip-sample distances at which the EPR resonance shift caused by the magnetic field of the tip is minimized. To this end, we measure the dependence of the resonance field on the tip-sample distance at different radiofrequencies and identify specific distances for which the true magnetic moment is found. Additionally, we show that the tip's influence can be averaged out by using magnetically bistable tips, which provides a complementary method to accurately measure the magnetic moment of surface atoms using EPR STM.

Application of EPR Spectroscopy in TiO2 and Nb2O5 Photocatalysis

The interaction of light with semiconducting materials becomes the center of a wide range of technologies, such as photocatalysis. This technology has recently attracted increasing attention due to its prospective uses in green energy and environmental remediation. The characterization of the electronic structure of the semiconductors is essential to a deep understanding of the photocatalytic process since they influence and govern the photocatalytic activity by the formation of reactive radical species. Electron paramagnetic resonance (EPR) spectroscopy is a unique analytical tool that can be employed to monitor the photoinduced phenomena occurring in the solid and liquid phases and provides precise insights into the dynamic and reactivity of the photocatalyst under different experimental conditions. This review focus on the application of EPR in the observation of paramagnetic centers formed upon irradiation of titanium dioxide and niobium oxide photocatalysts. TiO2 and Nb2O5 are very well-known semiconductors that have been widely used for photocatalytic applications. A large number of experimental results on both materials offer a reliable platform to illustrate the contribution of the EPR studies on heterogeneous photocatalysis, particularly in monitoring the photogenerated charge carriers, trap states, and surface charge transfer steps. A detailed overview of EPR-spin trapping techniques in mechanistic studies to follow the nature of the photogenerated species in suspension during the photocatalytic process is presented. The role of the electron donors or the electron acceptors and their effect on the photocatalytic process in the solid or the liquid phase are highlighted.

Rapid Scan EPR Oxygen Imaging in Photoactivated Resin Used for Stereolithographic 3D Printing.

Oxygen plays a critical role in the photopolymerization process resulting in the formation of solid structures from liquid resins during three-dimensional (3D) printing: it acts as a polymerization inhibitor. Upon exposure to light, oxygen is depleted. As a result, the polymerization process becomes activated. Electron paramagnetic resonance (EPR) imaging is described as a tool to visualize changes in oxygen distribution caused by light exposure. This nondestructive method uses radio waves and, therefore, is not constrained by optical opacity offering greater penetrating depth. Three proof-of-principle imaging experiments were demonstrated: (1) spatial propagation of the photopolymerization process; (2) oxygen depletion as a result of postcuring; and (3) oxygen visualization in a 3D printed spiral model. Commercial stereolithography (SLA) resin was used in these experiments. Lithium octa-n-butoxynaphthalocyanine (LiNc-BuO) probe was mixed with the resin to permit oxygen imaging. Li-naphthalocyanine probes are routinely used in various EPR applications because of their long-term stability and high functional sensitivity to oxygen. In this study, we demonstrate that EPR imaging has the potential to become a powerful visualization tool in the development of 3D printing technology, including bioprinting and tissue engineering.

A general model to optimise CuII labelling efficiency of double-histidine motifs for pulse dipolar EPR applications.

Electron paramagnetic resonance (EPR) distance measurements are making increasingly important contributions to studies of biomolecules underpinning health and disease by providing highly accurate and precise geometric constraints. Combining double-histidine (dH) motifs with CuII spin labels shows promise for further increasing the precision of distance measurements, and for investigating subtle conformational changes. However, non-covalent coordination-based spin labelling is vulnerable to low binding affinity. Dissociation constants of dH motifs for CuII-nitrilotriacetic acid were previously investigated via relaxation induced dipolar modulation enhancement (RIDME), and demonstrated the feasibility of exploiting the dH motif for EPR applications at sub-μM protein concentrations. Herein, the feasibility of using modulation depth quantitation in CuII-CuII RIDME to simultaneously estimate a pair of non-identical independent KD values in such a tetra-histidine model protein is addressed. Furthermore, we develop a general speciation model to optimise CuII labelling efficiency, depending upon pairs of identical or disparate KD values and total CuII label concentration. We find the dissociation constant estimates are in excellent agreement with previously determined values, and empirical modulation depths support the proposed model.

Electron paramagnetic resonance (EPR) spectroscopy: Food, biomedical and pharmaceutical analysis

Electron paramagnetic resonance (EPR) spectroscopy can be applied as an effective and non-invasive spectroscopic method for analyzing samples with unpaired electrons. EPR is suitable for the quantification of radical species, assessment of redox chemical reaction mechanisms in foods, evaluation of the antioxidant capacity of food, as well as for the analysis of food quality, stability, and shelf life. It can be employed for evaluating and monitoring the drug release processes, in vitro and in vivo. EPR can be employed for the direct detection of free radical metabolites, and the evaluation of drug release mechanisms from biodegradable polymers; it can be employed for analyzing the drug antioxidant effects. Additionally, spatial resolution can be achieved through EPR-imaging. EPR spectroscopy and imaging have shown diverse applications in food, biomedical and pharmaceutical fields, and also more applications are predictable to emerge in the future. This review highlights recent advances and important challenges related to the application of EPR in food, biomedical and pharmaceutical analysis and assessment.

ESR Method in Monitoring of Nanoparticle Endocytosis in Cancer Cells.

Magnetic nanoparticles are extensively studied for their use in diagnostics and medical therapy. The behavior of nanoparticles after adding them to cell culture is an essential factor (i.e., whether they attach to a cell membrane or penetrate the membrane and enter into the cell). The present studies aimed to demonstrate the application of electron spin resonance (ESR) as a suitable technique for monitoring of nanoparticles entering into cells during the endocytosis process. The model nanoparticles were composed of magnetite iron (II, III) oxide core functionalized with organic unit containing nitroxide radical 4-hydroxy-TEMPO (TEMPOL). The research studies included breast cancer cells, as well as model yeast and human microvascular endothelial cells. The results confirmed that the ESR method is suitable for studying the endocytosis process of nanoparticles in the selected cells. It also allows for direct monitoring of radical cellular processes.

Aqueous-Phase Decomposition of Isoprene Hydroxy Hydroperoxide and Hydroxyl Radical Formation by Fenton-like Reactions with Iron Ions.

Isoprene hydroxy hydroperoxides (ISOPOOH) formed by the photooxidation of isoprene under low-NO conditions play an important role in the formation and evolution of secondary organic aerosols, yet multiphase processes of ISOPOOH are poorly understood. By applying electron paramagnetic resonance spectroscopy, we observe that ISOPOOH undergoes aqueous-phase decomposition upon interacting with Fe(II) ions to form OH and organic radicals at room temperature. To reproduce the measured dependence of OH formation on the Fe concentrations by kinetic modeling, we postulate that Fe(II) ions react with ISOPOOH via Fenton-like reactions to form OH radicals with a rate constant of 7.3 × 10-18 cm3 s-1. At low concentrations, oxalate forms monocomplexes with Fe(II) ions, which can promote OH formation by ISOPOOH. However, at high concentrations, oxalate scavenges OH radicals, thereby lowering aqueous OH concentrations. These findings provide new insight for the atmospheric fate of ISOPOOH and reactive oxygen species generation in the aqueous phase.

Synthesis and coherent properties of 13C-enriched sub-micron diamond particles with nitrogen vacancy color centers

Here we report the synthesis of 13C-enriched diamond powder with sub-micron particle sizes via High Pressure High Temperature (HPHT) growth. Diamond powder with a tailored isotopic enrichment is particularly interesting for implementation of Dynamic Nuclear spin Polarization (DNP) and 13C enrichment plays an important role for increasing the signal to noise ratio in Nuclear Magnetic Resonance (NMR) and Magnetic Resonance Imaging. We applied Electron Paramagnetic Resonance (EPR) and NMR spectroscopy to the sub-micron diamond material as well as Optically Detected Magnetic Resonance (ODMR) and atomic force microscopy to investigate preselected nano-sized particles. The 13C spin concentrations were evaluated with NMR for the initial particle ensemble and with ODMR for the nanodiamond fraction, showing the homogeneous distribution of 13C density in particles with different sizes. The 13C nuclear spin-lattice relaxation decay (T1) shows a multiexponential behavior, where the fast relaxing component is attributed to relaxation from surface defects. Additionally, an optical method for estimating the NV− concentration in nanodiamonds is presented. The obtained powder is promising as a base material for the production of 13C-enriched nanodiamonds for DNP applications.

An investigation on geometry and metal interactions in multi metallic porphyrin complexes – EPR studies [microwave power saturation and degree of covalency

Innovative stylish materials can be synthesized and designed at the molecular level by attaching well characterized and tailored functionalities that have various applications. A series of meso-tetracuperated porphyrin-Schiff base complexes has been prepared from metallo-5,10,15,20-tetrakis(4-hydroxyphenyl) porphyrins (M = Cu(II), VO(II) and Ni(II)) and salicylideneamino-2-(N,N-dimethylamino)ethane copper(II) perchlorate under a nitrogen atmosphere and their electron paramagnetic resonance (EPR) spectra have been studied. The steric hindrance and electronic effects of the substituted groups and the characteristics of the different metal ions are the major patrons in inducing the properties of the compounds. From detailed spectral analysis and complete simulation, the results reveal a dipolar interaction between the central copper metal ion of the porphyrin and the meso-copper ions, but no interaction between the vanadyl group and the meso-copper ions. Through studying the EPR properties of these compounds, it is clear that novel EPR oximetry materials can be found and this will help to extend the applications of EPR in vivo.

EPR imaging of magnetic field effects on radiation dose distributions around millimeter-size air cavities

New hybrid radiotherapy treatment systems combining an MRI scanner with a source of ionizing radiation are being introduced in the clinic. The strong magnetic fields of MRI considerably affect radiation dose distributions, especially at tissue-air interfaces due to the electron return effect (ERE). Experimental investigation of the ERE within a sub-millimeter thick surface layer is still highly challenging.In the present work, we examine and quantify the magnetic field induced perturbations of dose distributions within a 0.5 mm layer surrounding millimeter-size air cavities by applying electron paramagnetic resonance imaging (EPRI).Air-filled fused quartz tubes (inner diameter 3 or 4 mm) mimic small air cavities and serve as model systems. The tubes were irradiated inside a PMMA phantom by a 6 MV photon beam. The irradiations were performed in the presence or absence of a transverse, magnetic field providing a magnetic field strength of 1.0 Tesla. The spatial distributions of radiation induced paramagnetic defects in the quartz tubes were subsequently determined by applying field-swept echo-detected EPRI and were then converted to relative dose distributions.The transverse magnetic field leads to considerable local dose enhancements and reductions (up to 35%) with respect to the mean dose within the quartz tubes. The experimentally determined dose distributions are in good quantitative agreement with Monte Carlo radiation transport simulations.The results of this work demonstrate the feasibility of field-swept echo-detected EPRI to measure magnetic field induced perturbations of dose distributions within a sub-millimeter thick surface layer at the dosimeter-air interface.

Precise Measurement and Controlled Tuning of Effective Window Sizes in ZIF-8 Framework for Efficient Separation of Xylenes.

Metal-organic frameworks (MOFs) are the promising nanomaterials for separation of molecules with close dimensions and structures, such as various types of isomers. The efficiency of separation can be greatly enhanced if the apertures of the nanosized windows, controlling the diffusion of a particular molecule inside the cavities, are fine-tuned by external stimuli. We report the new approach for precise measurement of window sizes in ZIF-8 MOF and employ it in efficient separation of xylenes, which is of high practical importance. For this sake, we synthesized ZIF-8 with embedded stable nitroxides in the pores and applied electron paramagnetic resonance spectroscopy for in situ kinetic measurement of the diffusion of various guest molecules through the material. Slight variation of temperature within 298-333 K allowed tuning of the windows and reaching optimum conditions for separation of p-, m-, and o-xylenes with the efficiency up to 92-95%. The developed methodology provides deeper understanding of steric and kinetic aspects of molecular diffusion in ZIF-8 and paves the way to rational optimization of other MOF-based separation applications.