يعرض 1 - 10 نتائج من 14 نتيجة بحث عن '"Melissa C. Piontek"', وقت الاستعلام: 0.92s تنقيح النتائج
  1. 1
    دورية أكاديمية

    المؤلفون: Melissa C. Piontek, Wouter H. Roos

    المصدر: Journal of Extracellular Biology, Vol 1, Iss 12, Pp n/a-n/a (2022)

    الوصف: Abstract Lipoproteins (LPs) are micelle‐like structures with a similar size to extracellular vesicles (EVs) and are therefore often co‐isolated, as intensively discussed within the EV community. LPs from human blood plasma are of particular interest as they are responsible for the deposition of cholesterol ester and other fats in the artery, causing lesions, and eventually atherosclerosis. Plasma lipoproteins can be divided according to their size, density and composition into chylomicrons (CM), very‐low‐density lipoproteins (VLDL), low‐density lipoproteins (LDL) and high‐density lipoproteins (HDL). Here, we use atomic force microscopy for mechanical characterization of LPs. We show that the nanoindentation approach used for EV analysis can also be used to characterize LPs, revealing specific differences between some of the particles. Comparing LPs with each other, LDL exhibit a higher bending modulus as compared to CM and VLDL, which is likely related to differences in cholesterol and apolipoproteins. Furthermore, CM typically collapse on the surface after indentation and HDL exhibit a very low height after surface adhesion both being indications for the presence of LPs in an EV sample. Our analysis provides new systematic insights into the mechanical characteristics of LPs.

    وصف الملف: electronic resource

  2. 2
    دورية أكاديمية

    المصدر: Nature Communications, Vol 9, Iss 1, Pp 1-9 (2018)

    مصطلحات موضوعية: Science

    الوصف: Red blood cell disorders are often accompanied by increased release of extracellular vesicles (EVs), but their structural and mechanical properties are not fully understood. Here, the authors show that red blood cell EVs show liposome-like mechanical features and are softened in blood disorder patients.

    وصف الملف: electronic resource

  3. 3
    دورية أكاديمية

    المصدر: Frontiers in Molecular Biosciences, Vol 7 (2020)

    الوصف: Both natural as well as artificial vesicles are of tremendous interest in biology and nanomedicine. Small vesicles (

    وصف الملف: electronic resource

  4. 4

    المساهمون: Physics of Living Systems, LaserLaB - Molecular Biophysics, Functional Genomics, Molecular Biophysics, Human genetics, Amsterdam Neuroscience - Cellular & Molecular Mechanisms

    المصدر: Sorkin, R, Marchetti, M, Logtenberg, E, Piontek, M C, Kerklingh, E, Brand, G, Voleti, R, Rizo, J, Roos, W H, Groffen, A J & Wuite, G J L 2020, ' Synaptotagmin-1 and Doc2b Exhibit Distinct Membrane-Remodeling Mechanisms ', Biophysical Journal, vol. 118, no. 3, pp. 643-656 . https://doi.org/10.1016/j.bpj.2019.12.021
    Biophysical Journal, 118(3), 643-656. Biophysical Society
    Biophysical Journal, 118(3), 643-656. CELL PRESS
    Biophys J

    الوصف: Synaptotagmin-1 (Syt1) is a calcium sensor protein that is critical for neurotransmission and is therefore extensively studied. Here, we use pairs of optically trapped beads coated with SNARE-free synthetic membranes to investigate Syt1-induced membrane remodeling. This activity is compared with that of Doc2b, which contains a conserved C2AB domain and induces membrane tethering and hemifusion in this cell-free model. We find that the soluble C2AB domain of Syt1 strongly affects the probability and strength of membrane-membrane interactions in a strictly Ca2+- and protein-dependent manner. Single-membrane loading of Syt1 yielded the highest probability and force of membrane interactions, whereas in contrast, Doc2b was more effective after loading both membranes. A lipid-mixing assay with confocal imaging reveals that both Syt1 and Doc2b are able to induce hemifusion; however, significantly higher Syt1 concentrations are required. Consistently, both C2AB fragments cause a reduction in the membrane-bending modulus, as measured by a method based on atomic force microscopy. This lowering of the energy required for membrane deformation may contribute to Ca2+-induced fusion.

    وصف الملف: application/pdf

  5. 5

    المساهمون: Molecular Biophysics

    المصدر: Biochimica et Biophysica Acta-General Subjects, 1865(4):129486. ELSEVIER SCIENCE BV

    الوصف: Background The interest in mechanics of synthetic and biological vesicles has been continuously growing during the last decades. Liposomes serve as model systems for investigating fundamental membrane processes and properties. More recently, extracellular vesicles (EVs) have been investigated mechanically as well. EVs are widely studied in fundamental and applied sciences, but their material properties remained elusive until recently. Elucidating the mechanical properties of vesicles is essential to unveil the mechanisms behind a variety of biological processes, e.g. budding, vesiculation and cellular uptake mechanisms. Scope of review The importance of mechanobiology for studies of vesicles and membranes is discussed, as well as the different available techniques to probe their mechanical properties. In particular, the mechanics of vesicles and membranes as obtained by nanoindentation, micropipette aspiration, optical tweezers, electrodeformation and electroporation experiments is addressed. Major conclusions EVs and liposomes possess an astonishing rich, diverse behavior. To better understand their properties, and for optimization of their applications in nanotechnology, an improved understanding of their mechanical properties is needed. Depending on the size of the vesicles and the specific scientific question, different techniques can be chosen for their mechanical characterization. General significance Understanding the mechanical properties of vesicles is necessary to gain deeper insight in the fundamental biological mechanisms involved in vesicle generation and cellular uptake. This furthermore facilitates technological applications such as using vesicles as targeted drug delivery vehicles. Liposome studies provide insight into fundamental membrane processes and properties, whereas the role and functioning of EVs in biology and medicine are increasingly elucidated.

    وصف الملف: application/pdf

  6. 6

    المساهمون: Molecular Biophysics, LaserLaB - Molecular Biophysics, Physics of Living Systems

    المصدر: Nature Communications, 9(1):4960. Nature Publishing Group
    Nature Communications, Vol 9, Iss 1, Pp 1-9 (2018)
    Nature Communications
    Nature Communications, 9(1). Nature Publishing Group
    Vorselen, D, van Dommelen, S M, Sorkin, R, Piontek, M C, Schiller, J, Döpp, S T, Kooijmans, S A A, van Oirschot, B A, Versluijs, B A, Bierings, M B, van Wijk, R, Schiffelers, R M, Wuite, G J L & Roos, W H 2018, ' The fluid membrane determines mechanics of erythrocyte extracellular vesicles and is softened in hereditary spherocytosis ', Nature Communications, vol. 9, 4960, pp. 1-9 . https://doi.org/10.1038/s41467-018-07445-x
    Nature Communications, 9:4960, 1-9. Nature Publishing Group

    الوصف: Extracellular vesicles (EVs) are widely studied regarding their role in cell-to-cell communication and disease, as well as for applications as biomarkers or drug delivery vehicles. EVs contain membrane and intraluminal proteins, affecting their structure and thereby likely their functioning. Here, we use atomic force microscopy for mechanical characterization of erythrocyte, or red blood cell (RBC), EVs from healthy individuals and from patients with hereditary spherocytosis (HS) due to ankyrin deficiency. While these EVs are packed with proteins, their response to indentation resembles that of fluid liposomes lacking proteins. The bending modulus of RBC EVs of healthy donors is ~15 kbT, similar to the RBC membrane. Surprisingly, whereas RBCs become more rigid in HS, patient EVs have a significantly (~40%) lower bending modulus than donor EVs. These results shed light on the mechanism and effects of EV budding and might explain the reported increase in vesiculation of RBCs in HS patients.
    Red blood cell disorders are often accompanied by increased release of extracellular vesicles (EVs), but their structural and mechanical properties are not fully understood. Here, the authors show that red blood cell EVs show liposome-like mechanical features and are softened in blood disorder patients.

    وصف الملف: application/pdf; image/pdf

  7. 7

    المساهمون: Physics of Living Systems, LaserLaB - Molecular Biophysics, Molecular Biophysics

    المصدر: Frontiers in Molecular Biosciences, 7(July):139, 1-14. Frontiers Media S.A.
    Frontiers in Molecular Biosciences, 7:139. Frontiers Media S.A.
    Frontiers in Molecular Biosciences, Vol 7 (2020)
    Frontiers in Molecular Biosciences
    Vorselen, D, Piontek, M C, Roos, W H & Wuite, G J L 2020, ' Mechanical Characterization of Liposomes and Extracellular Vesicles, a Protocol ', Frontiers in Molecular Biosciences, vol. 7, no. July, 139, pp. 1-14 . https://doi.org/10.3389/fmolb.2020.00139

    الوصف: Both natural as well as artificial vesicles are of tremendous interest in biology and nanomedicine. Small vesicles (

    وصف الملف: application/pdf

  8. 8
  9. 9

    الوصف: While the role of Synaptotagmin-1 in living cells has been described in detail, it remains a challenge to dissect the contribution of membrane remodelling by its two cytoplasmic C2 domains (C2AB) to the Ca2+-secretion coupling mechanism. Here, we study membrane remodeling using pairs of optically-trapped beads coated with SNARE-free synthetic membranes. We find that the soluble C2AB domain of Syt1 strongly affects the probability and strength of membrane-membrane interactions in a strictly Ca2+- and protein-dependent manner. A lipid mixing assay with confocal imaging reveals that at low Syt1 concentrations, no hemifusion is observed. Notably, for similar low concentrations of Doc2b hemifusion does occur. Consistently, both C2AB fragments cause a reduction in the membrane bending modulus, as measured by an AFM-based method. This lowering of the energy required for membrane deformation likely contributes to the overall Ca2+-secretion triggering mechanism by calcium sensor proteins. When comparing symmetrical (both sides) and asymmetrical (one side) presence of protein on the membranes, Syt1 favors an asymmetrical but Doc2b a symmetrical configuration, as inferred from higher tether probabilities and break forces. This provides support for the direct bridging hypothesis for Syt-1, while hinting to possible preference for protein-protein (and not protein-membrane) interactions for Doc2b. Overall, our study sheds new light on the mechanism of Ca2+ induced fusion triggering, which is essential for fundamental understanding of secretion of neurotransmitters and endocrine substances.

  10. 10

    المؤلفون: Melissa C, Piontek, Wouter H, Roos

    المصدر: Methods in molecular biology (Clifton, N.J.). 1665

    مصطلحات موضوعية: Nanotechnology, Proteins, Microscopy, Atomic Force

    الوصف: Imaging of nano-sized particles and sample features is crucial in a variety of research fields. For instance in biological sciences, where it is paramount to investigate structures at the single particle level. Often two-dimensional images are not sufficient and further information such as topography and mechanical properties are required. Furthermore, to increase the biological relevance, it is desired to perform the imaging in close to physiological environments. Atomic force microscopy (AFM) meets these demands in an all-in-one instrument. It provides high-resolution images including surface height information leading to three-dimensional information on sample morphology. AFM can be operated both in air and in buffer solutions. Moreover, it has the capacity to determine protein and membrane material properties via the force spectroscopy mode. Here we discuss the principles of AFM operation and provide examples of how biomolecules can be studied. By including new approaches such as high-speed AFM (HS-AFM) we show how AFM can be used to study a variety of static and dynamic single biomolecules and biomolecular assemblies.