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    Increase in the β-sheet character of an amyloidogenic peptide upon adsorption onto gold and silver surfaces

    , Article ChemPhysChem ; Volume 18, Issue 5 , 2017 , Pages 526-536 ; 14394235 (ISSN) Soltani, N ; Gholami, M. R ; Sharif University of Technology
    Wiley-VCH Verlag  2017
    Abstract
    Fibrillation of amyloid beta (Aβ) peptide is the hallmark of Alzheimer's disease. Given that interactions at the bio–nano interface affect the fibrillation tendency of this peptide, an understanding of the interactions at Aβ peptide–inorganic surfaces on the microscopic level can help to determine the possible neurotoxicity of nanoparticles. Here, the interactions between a fibril-forming peptide, Aβ25–35, and (111) and (100) facets of gold and silver surfaces have been studied by conducting atomistic molecular dynamics simulations. The obtained results indicate that the adsorption onto gold and silver surfaces force the peptide into the β-sheet-rich conformations, which is prone to... 

    Three-body interactions improve the prediction of rate and mechanism in protein folding models

    , Article Proceedings of the National Academy of Sciences of the United States of America ; Volume 101, Issue 42 , 2004 , Pages 15088-15093 ; 00278424 (ISSN) Ejtehadi, M. R ; Avall, S. P ; Plotkin, S. S ; Sharif University of Technology
    2004
    Abstract
    Here we study the effects of many-body interactions on rate and mechanism in protein folding by using the results of molecular dynamics simulations on numerous coarse-grained Cα-model single-domain proteins. After adding three-body interactions explicitly as a perturbation to a Gō-like Hamiltonian with native pairwise interactions only, we have found (i) a significantly increased correlation with experimental φ values and folding rates, (ii) a stronger correlation of folding rate with contact order, matching the experimental range in rates when the fraction of three-body energy in the native state is ≈20%, and (iii) a considerably larger amount of three-body energy present in chymotripsin... 

    Comparing EC and GO Model in Protein Folding Simulation

    , M.Sc. Thesis Sharif University of Technology Mohseni Kabir, Arman (Author) ; Ejtehadi, Mohammad Reza (Supervisor)
    Abstract
    Proteins are one of the most important bio-molecules. they play an important role in every aspect of living organisms. The information for synthesizing these important molecules is coded in the DNA of that organism. After the coded data is read and transcribed by some other bio-molecules that are proteins themselves, the protein is made and starts it's biological function in different organs. For this reason, investigating properties of proteins helps us to better understand how life works. Understanding the dynamics of proteins, which are some polymers with special energy landscape properties, has attracted the attention of physicists in the 20th century. Proteins are chains of amino... 

    Feature Extraction for Protein Sequences Based on NMR Spectra and Its Application in the Protein Interaction Prediction

    , M.Sc. Thesis Sharif University of Technology Teimoori, Bahareh (Author) ; Hajsadeghy, Khosro (Supervisor) ; Kavousi, Kaveh (Supervisor)
    Abstract
    Nuclear magnetic resonance is a spectroscopic method which is used to investigate characteristics of molecules with hydrogen and carbon chains. In this thesis we used, NMR spectrum extracted from 19 types of amino acids for investigating on feature generation for protein sequences. We processed NMR spectra based on Hydrogen and Carbon atoms in structure of the amino acids and after preprocessing we extracted features for each amino acid from the spectra. After that, we tried to cluster the amino acids with Fuzzy Clustering Method (FCM) then we generated feature vectors by extracting special descriptor for amino acids in sequence of proteins. In addition to NMR, we used the features of... 

    Molecular simulation of protein dynamics in nanopores. I. Stability and folding

    , Article Journal of Chemical Physics ; Volume 128, Issue 11 , 2008 ; 00219606 (ISSN) Javidpour, L ; Rahimi Tabar, M. R ; Sahimi, M ; Sharif University of Technology
    2008
    Abstract
    Discontinuous molecular dynamics simulations, together with the protein intermediate resolution model, an intermediate-resolution model of proteins, are used to carry out several microsecond-long simulations and study folding transition and stability of α -de novo-designed proteins in slit nanopores. Both attractive and repulsive interaction potentials between the proteins and the pore walls are considered. Near the folding temperature Tf and in the presence of the attractive potential, the proteins undergo a repeating sequence of folding/partially folding/unfolding transitions, with Tf decreasing with decreasing pore sizes. The unfolded states may even be completely adsorbed on the pore's... 

    A simple 2-step purification process of α-amylase from bacillus subtilis: optimization by response surface methodology

    , Article International Journal of Biological Macromolecules ; Volume 192 , 2021 , Pages 64-71 ; 01418130 (ISSN) Ataallahi, E ; Naderi-Manesh, H ; Roostaazad, R ; Yeganeh, S ; Sharif University of Technology
    Elsevier B.V  2021
    Abstract
    Purification of extracellular α-amylase from Bacillus subtilis was carried out via fractional precipitation by acetone and ion exchange chromatography. These steps provide fast precipitation as well as purification of α-amylase to improve enzyme purity, activity and stability. Compared with two-phase methods in which the yield was less than 1, this method resulted in a yield of more than 3. Moreover, 95% of acetone was recovered that enhanced the economy of the downstream process. Using the data provided by 2D electrophoresis, purification was done by a single step ion exchange chromatography. The enzyme exhibited a molecular mass (SDS-PAGE) of 50KD and the pI of 5. Maximum “yield” and... 

    Chaperones promote remarkable solubilization of salmonella enterica serovar enteritidis flagellin expressed in escherichia coli

    , Article Protein and Peptide Letters ; Volume 27, Issue 3 , 2020 , Pages 210-218 Bakhtiarvand, B ; Sadeghi, Z ; Tarahomjoo, S ; Yaghmaie, S ; Sharif University of Technology
    Bentham Science Publishers  2020
    Abstract
    Background: Flagellin of Salmonella enterica serovar Enteritidis (SEF) stimulates immune responses to both itself and coapplied antigens. It is therefore used in vaccine development and immunotherapy. Removal of pathogenic S. enterica ser. Enteritidis from SEF production process is advantageous due to the process safety improvement. The protein solubility analysis using SDS-PAGE indicated that 53.49% of SEF expressed in Escherichia coli formed inclusion bodies. However, the protein recovery from inclusion bodies requires a complex process with a low yield. Objective: We thus aim to study possibility of enhancing SEF expression in E. coli in soluble form using chemical and molecular... 

    Two-compartment processing as a tool to boost recombinant protein production

    , Article Engineering in Life Sciences ; Vol. 14, issue. 2 , March , 2014 , p. 118-128 Jazini, M ; Herwig, C ; Sharif University of Technology
    Abstract
    Pichia pastoris is used extensively as a production platform for many recombinant proteins. The dissolved oxygen (DO) is one of the most important factors influencing protein production. The influence of the DO on productivity has not been studied independent from the feed rate. In this work, various DO levels were investigated independent from the feed rate. The model system was recombinant P. pastoris under the control of methanol-induced alcohol oxidase promoter, which expressed HRP as the target protein. No significant effect was observed in terms of titer and specific productivity, which is a confirmation of the fact that the DO in a one-compartment system cannot boost productivity for... 

    Power of a remote hydrogen bond donor: Anion recognition and structural consequences revealed by IR spectroscopy

    , Article Journal of Organic Chemistry ; Volume 80, Issue 2 , December , 2015 , Pages 1130-1135 ; 00223263 (ISSN) Samet, M ; Danesh Yazdi, M ; Fattahi, A ; Kass, S. R ; Sharif University of Technology
    American Chemical Society  2015
    Abstract
    Natural and synthetic anion receptors are extensively employed, but the structures of their bound complexes are difficult to determine in the liquid phase. Infrared spectroscopy is used in this work to characterize the solution structures of bound anion receptors for the first time, and surprisingly only two of three hydroxyl groups of the neutral aliphatic triols are found to directly interact with Cl-. The binding constants of these triols with zero to three CF3 groups were measured in a polar environment, and KCD3CN(Cl-) = 1.1 × 106 M-1 for the tris(trifluoromethyl) derivative. This is a remarkably large value, and high selectivity with respect to interfering anions such as, Br-, NO3 -... 

    Identification of an aspidospermine derivative from borage extract as an anti-amyloid compound: A possible link between protein aggregation and antimalarial drugs

    , Article Phytochemistry ; Volume 140 , 2017 , Pages 134-140 ; 00319422 (ISSN) Kalhor, H. R ; Ashrafian, H ; Sharif University of Technology
    Elsevier Ltd  2017
    Abstract
    A number of human diseases, including Alzheimer's and Parkinson's have been linked to amyloid formation. To search for an anti-amyloidogenic product, alkaloid enriched extract from borage leaves was examined for anti-amyloidogenic activity using Hen Egg White Lysozyme (HEWL) as a model protein. After isolation of the plant extract using rHPLC, only one fraction indicated a significant bioactivity. TEM analysis confirmed a remarkable reduction of amyloid fibrils in the presence of the bioactive fraction. To identify the effective substance in the fraction, mass spectrometry, FTIR, and NMR were performed. Our analyses determined that the bioactive compound as... 

    Amyloid fibril reduction through covalently modified lysine in HEWL and insulin

    , Article Archives of Biochemistry and Biophysics ; Volume 727 , 2022 ; 00039861 (ISSN) Rezaei, M ; Kalhor, H. R ; Sharif University of Technology
    Academic Press Inc  2022
    Abstract
    Proteins possess a variety of nucleophiles, which can carry out different reactions in the functioning cells. Proteins endogenously and synthetically can be modified through their nucleophilic sites. The roles of these chemical modifications have not been completely revealed. These modifications can alter the protein folding process. Protein folding directly affects the function of proteins. If an error in protein folding occurs, it may cause protein malfunction leading to several neurodegenerative disorders such as Alzheimer's and Parkinson's. In this study, Hen Egg White Lysozyme (HEWL) and bovine insulin, as model proteins for studying the amyloid formation, were covalently attached with... 

    Review on alzheimer's disease: inhibition of amyloid beta and tau tangle formation

    , Article International Journal of Biological Macromolecules ; Volume 167 , 2021 , Pages 382-394 ; 01418130 (ISSN) Ashrafian, H ; Hadi Zadeh, E ; Hasan Khan, R ; Sharif University of Technology
    Elsevier B.V  2021
    Abstract
    It is reported that approximately 40 million people are suffering from dementia, globally. Dementia is a group of symptoms that affect neurons and cause some mental disorders, such as losing memory. Alzheimer's disease (AD) which is known as the most common cause of dementia, is one of the top medical care concerns across the world. Although the exact sources of the disease are not understood, is it believed that aggregation of amyloid-beta (Aβ) outside of neuron cells and tau aggregation or neurofibrillary tangles (NFTs) formation inside the cell may play crucial roles. In this paper, we are going to review studies that targeted inhibition of amyloid plaque and tau protein tangle formation,...