Facilitated Diffusion
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Osmosis, Diffusion, and Membrane Transport Bio 219 Napa Valley College Dr
Osmosis, Diffusion, and Membrane Transport Bio 219 Napa Valley College Dr. Adam Ross Overview In order to understand how cells regulate themselves, we must first understand how things move into and out of cells Diffusion • Diffusion is the movement of particles from an area of high charge or concentration to an area of lower charge or concentration • Referred to as moving “down” a charge or concentration gradient • Ex. H+ ions in mitochondria moving through ATP synthase • Result of random molecular motion • Fick’s Law of Diffusion gives rate of diffusion: • Rate = P A (Cout – Cin) / (x) • Rate is proportional to permeability (P), surface area (A), concentration gradient (Cout – Cin); inversely proportional to diffusion distance or membrane thickness (x) Gradients • Concentration • Caused by unequal distribution of a substance on either side of the membrane • If the inside of a cell is negative, it will attract positively charged things • Electrical (charge) • Caused by unequal distribution of charge on either side of the membrane Diffusion Osmosis • Osmosis is the movement of solvent through a semi permeable membrane in order to balance the solute concentration on either side of the membrane. • In cells the solvent is water • Water can cross membranes Osmosis Osmolarity • Total concentration of all solutes in a solution • 1 Osm = 1 mole solute/ L • Have to account for both atoms in salts • 1M NaCl +1 L H2O → 1M Na+ + 1M Cl ≈ 2 Osm • Plasma = 290 mOsm Osmotic pressure • This is the actual driving force for net water movement • Depends on -
Membrane Transport, Absorption and Distribution of Drugs
Chapter 2 1 Pharmacokinetics: Membrane Transport, Absorption and Distribution of Drugs Pharmacokinetics is the quantitative study of drug movement in, through and out of the body. The overall scheme of pharmacokinetic processes is depicted in Fig. 2.1. The intensity of response is related to concentration of the drug at the site of action, which in turn is dependent on its pharmacokinetic properties. Pharmacokinetic considerations, therefore, determine the route(s) of administration, dose, and latency of onset, time of peak action, duration of action and frequency of administration of a drug. Fig. 2.1: Schematic depiction of pharmacokinetic processes All pharmacokinetic processes involve transport of the drug across biological membranes. Biological membrane This is a bilayer (about 100 Å thick) of phospholipid and cholesterol molecules, the polar groups (glyceryl phosphate attached to ethanolamine/choline or hydroxyl group of cholesterol) of these are oriented at the two surfaces and the nonpolar hydrocarbon chains are embedded in the matrix to form a continuous sheet. This imparts high electrical resistance and relative impermeability to the membrane. Extrinsic and intrinsic protein molecules are adsorbed on the lipid bilayer (Fig. 2.2). Glyco- proteins or glycolipids are formed on the surface by attachment to polymeric sugars, 2 aminosugars or sialic acids. The specific lipid and protein composition of different membranes differs according to the cell or the organelle type. The proteins are able to freely float through the membrane: associate and organize or vice versa. Some of the intrinsic ones, which extend through the full thickness of the membrane, surround fine aqueous pores. CHAPTER2 Fig. -
Cellular Transport Notes About Cell Membranes
Cellular Transport Notes @ 2011 Center for Pre-College Programs, New Jersey Institute of Technology, Newark, New Jersey About Cell Membranes • All cells have a cell membrane • Functions: – Controls what enters and exits the cell to maintain an internal balance called homeostasis TEM picture of a – Provides protection and real cell membrane. support for the cell @ 2011 Center for Pre-College Programs, New Jersey Institute of Technology, Newark, New Jersey 1 About Cell Membranes (continued) 1.Structure of cell membrane Lipid Bilayer -2 layers of phospholipids • Phosphate head is polar (water loving) Phospholipid • Fatty acid tails non-polar (water fearing) • Proteins embedded in membrane Lipid Bilayer @ 2011 Center for Pre-College Programs, New Jersey Institute of Technology, Newark, New Jersey Polar heads Fluid Mosaic love water Model of the & dissolve. cell membrane Non-polar tails hide from water. Carbohydrate cell markers Proteins @ 2011 Center for Pre-College Programs, New Jersey Institute of Technology, Newark, New Jersey 2 About Cell Membranes (continued) • 4. Cell membranes have pores (holes) in it • Selectively permeable: Allows some molecules in and keeps other molecules out • The structure helps it be selective! Pores @ 2011 Center for Pre-College Programs, New Jersey Institute of Technology, Newark, New Jersey Structure of the Cell Membrane Outside of cell Carbohydrate Proteins chains Lipid Bilayer Transport Protein Phospholipids Inside of cell (cytoplasm) @ 2011 Center for Pre-College Programs, New Jersey Institute of Technology, Newark, New Jersey 3 Types of Cellular Transport • Passive Transport celldoesn’tuseenergy 1. Diffusion 2. Facilitated Diffusion 3. Osmosis • Active Transport cell does use energy 1. -
CO2 Permeability of Biological Membranes and Role of CO2 Channels
membranes Review CO2 Permeability of Biological Membranes and Role of CO2 Channels Volker Endeward, Mariela Arias-Hidalgo, Samer Al-Samir and Gerolf Gros * Molekular-und Zellphysiologie, AG Vegetative Physiologie–4220–Medizinische Hochschule Hannover, 30625 Hannover, Germany; [email protected] (V.E.); [email protected] (M.A.-H.); [email protected] (S.A.-S.) * Correspondence: [email protected]; Fax: +49-511-5322938 Received: 17 September 2017; Accepted: 18 October 2017; Published: 24 October 2017 Abstract: We summarize here, mainly for mammalian systems, the present knowledge of (a) the membrane CO2 permeabilities in various tissues; (b) the physiological significance of the value of the CO2 permeability; (c) the mechanisms by which membrane CO2 permeability is modulated; (d) the role of the intracellular diffusivity of CO2 for the quantitative significance of cell membrane CO2 permeability; (e) the available evidence for the existence of CO2 channels in mammalian and artificial systems, with a brief view on CO2 channels in fishes and plants; and, (f) the possible significance of CO2 channels in mammalian systems. Keywords: CO2 permeability; membrane cholesterol; protein CO2 channels; aquaporins; Rhesus proteins; aquaporin-1-deficient mice 1. Introduction This review intends to update the state of this field as it has been given by Endeward et al. [1] in 2014. In addition, we attempt to give a compilation of all of the lines of evidence that have so far been published demonstrating the existence of protein CO2 channels and their contributions to membrane CO2 permeability. We also give a compilation of the recently described remarkable variability of the CO2 permeability in mammalian cell membranes. -
Hollow Fiber Membrane Contactors for Post-Combustion Carbon Capture: a Review of Modeling Approaches
membranes Review Hollow Fiber Membrane Contactors for Post-Combustion Carbon Capture: A Review of Modeling Approaches Joanna R. Rivero 1 , Grigorios Panagakos 2,∗ , Austin Lieber 1 and Katherine Hornbostel 1 1 Department of Mechanical Engineering and Material Science, University of Pittsburgh, 3700 O’Hara St, Pittsburgh, PA 15213, USA; [email protected] (J.R.R.); [email protected] (A.L.); [email protected] (K.H.) 2 Department of Chemical Engineering, Carnegie Mellon University, 5000 Forbes Ave, Pittsburgh, PA 15213, USA * Correspondence: [email protected] Received: 30 October 2020; Accepted: 25 November 2020; Published: 30 November 2020 Abstract: Hollow fiber membrane contactors (HFMCs) can effectively separate CO2 from post-combustion flue gas by providing a high contact surface area between the flue gas and a liquid solvent. Accurate models of carbon capture HFMCs are necessary to understand the underlying transport processes and optimize HFMC designs. There are various methods for modeling HFMCs in 1D, 2D, or 3D. These methods include (but are not limited to): resistance-in-series, solution-diffusion, pore flow, Happel’s free surface model, and porous media modeling. This review paper discusses the state-of-the-art methods for modeling carbon capture HFMCs in 1D, 2D, and 3D. State-of-the-art 1D, 2D, and 3D carbon capture HFMC models are then compared in depth, based on their underlying assumptions. Numerical methods are also discussed, along with modeling to scale up HFMCs from the lab scale to the commercial scale. Keywords: hollow fiber membrane contactor modeling; post-combustion carbon capture; carbon capture membrane modeling 1. Introduction In 2018, the Intergovernmental Panel on Climate Change issued a report detailing the irreversible impact of a global temperature rise of 1.5 ◦C[1]. -
Polymers and Solvents Used in Membrane Fabrication: a Review Focusing on Sustainable Membrane Development
University of Kentucky UKnowledge Chemical and Materials Engineering Faculty Publications Chemical and Materials Engineering 4-23-2021 Polymers and Solvents Used in Membrane Fabrication: A Review Focusing on Sustainable Membrane Development Xiaobo Dong University of Kentucky, [email protected] David Lu University of Kentucky, [email protected] Tequila A. L. Harris Georgia Institute of Technology Isabel C. Escobar University of Kentucky, [email protected] Follow this and additional works at: https://uknowledge.uky.edu/cme_facpub Part of the Chemical Engineering Commons, and the Materials Science and Engineering Commons Right click to open a feedback form in a new tab to let us know how this document benefits ou.y Repository Citation Dong, Xiaobo; Lu, David; Harris, Tequila A. L.; and Escobar, Isabel C., "Polymers and Solvents Used in Membrane Fabrication: A Review Focusing on Sustainable Membrane Development" (2021). Chemical and Materials Engineering Faculty Publications. 80. https://uknowledge.uky.edu/cme_facpub/80 This Review is brought to you for free and open access by the Chemical and Materials Engineering at UKnowledge. It has been accepted for inclusion in Chemical and Materials Engineering Faculty Publications by an authorized administrator of UKnowledge. For more information, please contact [email protected]. Polymers and Solvents Used in Membrane Fabrication: A Review Focusing on Sustainable Membrane Development Digital Object Identifier (DOI) https://doi.org/10.3390/membranes11050309 Notes/Citation Information Published in Membranes, v. 11, issue 5, 309. © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). -
Cell Transport
Cells and their Environment Transport occurs across the cell membrane and helps a cell to maintain homeostasis. Cell part responsible: 5/16/14 1 1. Movement of materials across the membrane is called transport. A. Passive Transport - WITHOUT the use of energy • Driven by Kinetic energy/Brownian motion B. Active Transport - WITH the use of energy- against a concentration gradient 5/16/14 2 2. Concentration Gradient- difference in concentration from one area to another Visual Concept 5/16/14 3 3. Diffusion is passive/no energy. a) Diffusion- high to low concentration. b) Quicker at higher temps c) Occurs until an equilibrium is reached 5/16/14 4 4. Osmosis is the diffusion of water molecules directly through the cell's membrane. 5/16/14 5 5. If a cell is in a solution that is….. a) Hypertonic it shrinks (higher concentration of dissolved particles outside than inside of the cell) b) Hypotonic it expands (lower concentration of dissolved particles outside compared with inside of the cell) c) Isotonic no change (same concentration of dissolved particles outside as inside of the cell. 5/16/14 6 Graphic Organizer Hypertonic Hypotonic Isotonic DRAWINGS: For each category, draw a cell in solution. For each picture, show solute particles in your solution and also in your cell. Label solvent line and solute particles. Show if water is entering or leaving the cell using arrows. WRITE ABOUT IT: For each category, answer the following in complete sentences. 1) Is water moving into or out of the cell, or neither? 2) Is the cell shrinking, expanding or staying the same? 3) Are there more solute particles inside 5/16/14the cell or in solution, or neither? 7 Question: What would happen to an animal cell placed into a HYPERtonic solution? 5/16/14 8 (It would shrink- plasmolysis) 6. -
Atypical Solute Carriers
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine 1346 Atypical Solute Carriers Identification, evolutionary conservation, structure and histology of novel membrane-bound transporters EMELIE PERLAND ACTA UNIVERSITATIS UPSALIENSIS ISSN 1651-6206 ISBN 978-91-513-0015-3 UPPSALA urn:nbn:se:uu:diva-324206 2017 Dissertation presented at Uppsala University to be publicly examined in B22, BMC, Husargatan 3, Uppsala, Friday, 22 September 2017 at 10:15 for the degree of Doctor of Philosophy (Faculty of Medicine). The examination will be conducted in English. Faculty examiner: Professor Carsten Uhd Nielsen (Syddanskt universitet, Department of Physics, Chemistry and Pharmacy). Abstract Perland, E. 2017. Atypical Solute Carriers. Identification, evolutionary conservation, structure and histology of novel membrane-bound transporters. Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine 1346. 49 pp. Uppsala: Acta Universitatis Upsaliensis. ISBN 978-91-513-0015-3. Solute carriers (SLCs) constitute the largest family of membrane-bound transporter proteins in humans, and they convey transport of nutrients, ions, drugs and waste over cellular membranes via facilitative diffusion, co-transport or exchange. Several SLCs are associated with diseases and their location in membranes and specific substrate transport makes them excellent as drug targets. However, as 30 % of the 430 identified SLCs are still orphans, there are yet numerous opportunities to explain diseases and discover potential drug targets. Among the novel proteins are 29 atypical SLCs of major facilitator superfamily (MFS) type. These share evolutionary history with the remaining SLCs, but are orphans regarding expression, structure and/or function. They are not classified into any of the existing 52 SLC families. -
Comparison of Human Solute Carriers
Comparison of human solute carriers Avner Schlessinger,1,2,3* Pa¨ r Matsson,1,2,3 James E. Shima,1,2,3,4 Ursula Pieper,1,2,3 Sook Wah Yee,1,2,3 Libusha Kelly,1,2,3,5 Leonard Apeltsin,1,2,3,5 Robert M. Stroud,6 Thomas E. Ferrin,1,2,3 Kathleen M. Giacomini,1,2,3 and Andrej Sali1,2,3* 1Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, California 2Department of Pharmaceutical Chemistry, University of California, San Francisco, California 3California Institute for Quantitative Biosciences, University of California, San Francisco, California 4Graduate Program in Pharmaceutical Sciences and Pharmacogenomics, University of California, San Francisco, California 5Graduate Program in Biological and Medical Informatics, University of California, San Francisco, California 6Department of Biochemistry and Biophysics, University of California, San Francisco, California Received 14 August 2009; Revised 10 December 2009; Accepted 14 December 2009 DOI: 10.1002/pro.320 Published online 5 January 2010 proteinscience.org Abstract: Solute carriers are eukaryotic membrane proteins that control the uptake and efflux of solutes, including essential cellular compounds, environmental toxins, and therapeutic drugs. Solute carriers can share similar structural features despite weak sequence similarities. Identification of sequence relationships among solute carriers is needed to enhance our ability to model individual carriers and to elucidate the molecular mechanisms of their substrate specificity and transport. Here, we describe a comprehensive comparison of solute carriers. We link the proteins using sensitive profile–profile alignments and two classification approaches, including similarity networks. The clusters are analyzed in view of substrate type, transport mode, organism conservation, and tissue specificity. -
And Space-Saving Hollow Fiber Membrane Module Unit for Water Treatment
FEATURED TOPIC Energy- and Space-Saving Hollow Fiber Membrane Module Unit for Water Treatment Keiichi IKEDA*, Tomoyuki YONEDA, Shinsuke KAWABE, Hiroko MIKI, and Toru MORITA ---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- We have developed and marketed a new POREFLON membrane module unit for water treatment. It has a smaller footprint and is more energy saving than conventional products. In addition to the features of the conventional POREFLON hollow fiber membrane such as fouling resistance, high strength, and bending resistance, the module unit features the cassette type module structure, increased effective membrane length, enhanced packing density, and newly developed air diffusers that generate large air bubbles to prevent fouling. In a pilot test for municipal wastewater treatment jointly conducted with Japan Sewage Works Agency and others, we achieved a power consumption per unit of 0.4 kWh/m3 or lower, which was the target point for the popularization of membrane treatment. The module unit passed another several field trials and was currently commercialized. This report introduces the development process, product specifications, and case studies regarding the new membrane module unit. ---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- -
Chapter 7: Membranes
BIOL 1020 – CHAPTER 7 LECTURE NOTES Chapter 7: Membranes 1. What are the major roles of biological membranes? 2. What about phospholipids makes a bilayer when mixed with water? Use the term amphipathic, and contrast with what detergents do. 3. Describe the fluid mosaic model: what does it mean to have a 2-dimensional fluid and not a 3-dimensional one, and what does the “mosaic” term mean here? 4. Discuss membrane fluidity: why it is important and the ways it can be adjusted. 5. Contrast integral and peripheral membrane proteins. 6. Define and discuss these terms related to transport/transfer across cell membranes: selectively permeable diffusion concentration gradient osmosis tonics isotonic hypertonic hypotonic turgor pressure 7. What is carrier-mediated transport? Differentiate between facilitated diffusion and active transport. 8. Describe how the sodium-potassium pump works. 9. Explain linked cotransport. 10. Define the processes of exocytosis and endocytosis (include different forms of endocytosis). 11. Summarize processes for transport of materials across membranes; include information about which ones are active (energy-requiring). 12. Discuss information transfer across a membrane (signal transduction); why is it needed, what are some concepts that you should associate with it? 13. Differentiate between the following in terms of structure and function: anchoring junctions (such as desmosomes) tight junctions gap juntions plasmodesmata 1 of 7 BIOL 1020 – CHAPTER 7 LECTURE NOTES Chapter 7: Membranes I. Roles of biological membranes A. membranes separate aqueous environments, so that differences can be maintained 1. the plasma membrane surrounds the cell and separates the interior of the cell from the external environment 2. -
PINOCYTOSIS in FIBROBLASTS Quantitative Studies in Vitro
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by PubMed Central PINOCYTOSIS IN FIBROBLASTS Quantitative Studies In Vitro RALPH M. STEINMAN, JONATHAN M. SILVER, and ZANVIL A. COHN From The Rockefeller University, New York 10021 ABSTRACT Horseradish peroxidase (HRP) was used as a marker to determine the rate of ongoing pinocytosis in several fibroblast cell lines. The enzyme was interiorized in the fluid phase without evidence of adsorption to the cell surface. Cytochemical reaction product was not found on the cell surface and was visualized only within intracellular vesicles and granules. Uptake was directly proportional to the ad- ministered concentration of HRP and to the duration of exposure, The rate of HRP uptake was 0.0032-0.0035% of the administered load per 106 cells per hour for all ceils studied with one exception: L cells, after reaching confluence, pro- gressively increased their pinocytic activity two- to fourfold. After uptake of HRP, L cells inactivated HRP with a half-life of 6-8 h. Certain metabolic re- quirements of pinocytosis were then studied in detail in L cells. Raising the en- vironmental temperature increased pinocytosis over a range of 2-38°C. The Qlo was 2.7 and the activation energy, 17.6,kcal/mol. Studies on the levels of cellular ATP in the presence of various metabolic inhibitors (fluoride, 2-desoxyglycose, azide, and cyanide) showed that L cells synthesized ATP by both glycolytic and respiratory pathways. A combination of a glycolytic and a respiratory inhibitor was needed to depress cellular ATP levels as well as pinocytic activity to 10-20% of control values, whereas drugs administered individually had only partial ef- fects.