A Comprehensive Model of Multiprotein Adsorption on Surfaces
Adsorption
It occurs when a solution containing dissolved proteins comes into contact with a solid surface
The mechanism suggested here for protein adsorption is an extension of the classic reaction-diffusion mechanism which is followed by a wide variety of physical phenomena. The vroman effect arises when this basic mechanism is coupled with the presence of multiple proteins, each diffusing at different rates to the surface and engaging in competitive adsorption here.
All proteins have uniform concentration everywhere before the surface comes into contact with blood or any other multiprotein solution. Experiments show that upon contact with surface proteins are adsorbed as a monolayer.
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The rate at which reversibly adsorbed protein changes to irreversibly adsorbed protein depends on rate constant of irreversible adsorption, and on the concentration of reversibly adsorbed protein.
The driving force for increasing the surface affinity are: hydrophobicity of a surface (directly proportional, dominating factor), Electrostatic forces, Van der Waal forces, and Steric repulsion (in case surface is coated with a polymer such as polyethlylene oxide)
This study deals with uncoated surfaces in which first three kind of forces are active. The hydrophobic and van der Waal forces act in similar fashion, although hydrophobic forces are much larger.
Hence, adsorption is primarily caused by hydrophobic and van der Waal forces, with some electrostatic contribution.
Desorption occurs because the proteins in the solution modify the electrochemical environment or the adsorbed protein to overcome its hydrophobic attraction of the surface. It supports the fact that desorption does not occur in a protein free
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Every time a protein is displaced by another, a fraction of the first protein will remain on the surface. The magnitude of this fraction will depend on how long the protein remained on the surface before displacement, that is, on the time of two successive protein peaks. Larger differences in diffusivity and smaller differences in surface affinity will increase the tie between peaks, and consequently the magnitude of non-elutable protein on the surface and final composition of the adsorbed layer.
Finally, the flow of solution will increase the diffusion or transport rates of the all proteins to the surface. This in effect decrease the differences in diffusion rates and will cause all the protein peaks to occur earlier and cause a crowding of these peaks. Higher fluid flow rates will increase the crowding, although this does not qualitatively change the adsorption process.
Mathematical Model
Consider a multiprotein solution in contact with a surface below it at the point z=0, where z is the vertical distance in the solution measured from the surface. In the absence of convection, assuming that there are no horizontal concentration variations, the domain equation for species mass conservation is
(∂x_i)/∂t=D_i (∂^2 x_i)/(∂z^2 ) x = mole
Cadet Eric Wiggins Date: 18 September 2014 Course Name: Chem 100 Instructor: Captain Zuniga Section: M3A Identification of a Copper Mineral Intro Minerals are elements or compounds that are created in the Earth by geological processes. The method of isolating metals in a compound mineral is normally conducted through two processes.
In this lab, the water molecules stick strongly together and
To be more precise, its aggregation is mediated by β-site APP-cleaving enzyme 1 (BACE1) of the β-secretase and presenilin, which is the active site of the γ- secretase (Blennow,
Depending on if the compound is immiscible in water or not, the dissolved substances will have more attraction to one of the layers over the other, therefore separating the two different
Summary In this lab our primary goal was to learn about the kidney and its filtration abilities as well as how the kidneys maintain blood composition by altering the urine composition. As well as to see the effects glucose, protein, salt, and water intake have on the urine composition and volume. To do this we will use multistix test strips to test the urine before the intake in fluids and then once again after the glucose, protein, salt, or water is consumed. The last objective is to understand the relationship between urine output and various conditions and diseases, this is done through the use of several multistix test strips and descriptions of several people's characteristics and their diseases.
Proteins are made up of peptide bonds holding amino acids together to perform biological functions like enzymes, antibodies, for transport and structure (Asmus, 2007). Lastly, nucleic acids
. SUPER HYDROPHOBICITY Soumya Ranjan Sahoo (711CH1025) NIT, Rourkela Abstract: Superhydrophobicity as a sensation has turned into an increasing focus of research and technological movement, where its key viewpoints span surface chemistry, chemical physics, and cellular biology. Hydrophobic particles have a tendency to be non-polar and, accordingly, incline toward other neutral molecule and non-polar solvents. Hydrophobic atoms in water frequently bunch together, shaping micelles.
By Jonas Wilson Types of Capillary Electrophoresis In the evolution of techniques used to separate molecules based on their electrophoretic mobility, capillary electrophoresis has been fine-tuned in order to obtain optimal results for varying experiments. For the purposes of this article, six main forms of capillary electrophoresis, branching from two main subsets, one of which is further subdivided into two subdivisions, will be discussed. Generally, the two main subsets of capillary electrophoresis are a continuous system capillary electrophoresis and a discontinuous system capillary electrophoresis.
The higher the surface tension, The more molecules can stay together --------------------------------------------------------------------------------------------------V Viscosity questions A substance that has high viscosity is honey A substance that has low viscosity is water The viscosity range is
The size of the pore matters as well. Diffusion is when the movement of molecules from an area of high concentration to an low area concentration. Osmosis is the movement of water
Bio Chem lab Report 04 Enzyme Biochemistry Group Member: Chan Man Jeun Duncan (16002621) Law Sze Man (16000478) Introduction Enzyme is a protein base structure substance in our body. It works at a biocatalyst that will catalyzing the chemical reaction, which helps to speed up the chemical reaction. Enzyme could only function in specific shape, and the shape of enzyme is depending on the environment, therefore it is hard for an enzyme to function well in an extreme environment. The aim of this experiment is to see can the enzyme functions normally in different environment(pH, temperature and salt concentration) via using starch solution, amylase from saliva, 0.5M HCl solution, 0.5M NaOH solution and NaCl solution, and using iodine solution
Centrioles are non-membranous organelles that are usually located near the Golgi apparatus and the nucleus [30]. Most cells have two centrioles, each made up of nine sets of three microtubules (described later on page #39). Centrioles are hollow and cylindrical and lay next to each other at 90 degree angles [31]. Vital to cellular division, the centrioles function to separate homologous chromosomes in meiosis 1 and sister chromatids during mitosis and meiosis 2. During these processes, the centrioles form fibers, called spindle and aster fibers, which attach to the centromeres and line up the chromosomes or homologous pairs of chromosomes on the metaphase plate.
The concentration rate hypothesis was supported by the results that the enzyme absorption does increase as the concentration increases.
There are many factors which affects the rate of an enzyme catalyzed reaction. The rate of an enzyme controlled reaction is measured by 1.The amount of substrate change per unit time 2.The amount of product formed per unit time 3. The time taken for the completion of the reaction In investigating the effect of one factor : All the factors should be kept constant They must be maintained at suitable levels Only the initial rate should be measured.
The Effect of the Molecular Weight of a Substance to its Rate of Diffusion Paulo E. Garcia Group 2 Sec U-7L October 16, 2014 ABSTRACT The rate of diffusion was tested by using a petri dish with agar-water gel and three drops of different solutions. These solutions were observed for thirty minutes and measured every three minutes. The different solutions used are Potassium permanganate with a molecular weight of 158 g/mole diffused the greatest distance among the three, Potassium dichromate with a molecular weight of 294 g/mole diffused the lesser than that of Potassium permanganate, and Methylene Blue with a molecular weight of 374 g/mole diffused the least distance.