Non-fluorinated cosolvents: A potent amorphous aggregate inducer of metalloproteinase-conalbumin (ovotransferrin).

Here we have used five non-fluorinated cosolvents (acetonitrile, ethanol, methanol, sec-butanol and ter-butanol) at increasing concentrations and analyzed their aggregation inducing behavior on interaction with conalbumin (CA). The aggregates were identified as amorphous by performing spectroscopic experiments like circular dichroism and dye binding assay. The amorphous aggregate contains rich β-sheet content, show insignificant increment in Thioflavin-T (ThT) fluorescence intensity but strong 1-anilino-8-napthalene sulfonate (ANS) binding with enhanced fluorescence intensity. We also performed transmission electron microscope (TEM) and scanning electron microscope (SEM) imaging of the aggregates which made the result more informative. The morphology appeared on TEM imaging shows aggregates but there is no exhibition of fibril formation, as was observed in amyloid induced by 2,2,2-trifuoroethanol (TFE) and 1,1,1,3,3,3-hexafluoro-propan-2-ol (HFIP). SEM imaging also gives the similar results indicating the formation of amorphous aggregates. Web based tools (Waltz and AGGRESCAN) predicted aggregation prone regions in CA which are accountable for the aggregation.

[1]  Gabriel Keliényi ON THE HISTOCHEMISTRY OF AZO GROUP-FREE THIAZOLE DYES , 1967 .

[2]  R. Kuboi,et al.  Clustering of Fluorine-Substituted Alcohols as a Factor Responsible for Their Marked Effects on Proteins and Peptides , 1999 .

[3]  R. Truscott Age-related nuclear cataract-oxidation is the key. , 2005, Experimental eye research.

[4]  W. Huff,et al.  Identification of ovotransferrin as an acute phase protein in chickens. , 2002, Poultry science.

[5]  S. Aks,et al.  A visual schematic for clarifying the temporal relationship between the anion and osmol gaps in toxic alcohol poisoning. , 2003, The American journal of emergency medicine.

[6]  Wim Jiskoot,et al.  Extrinsic Fluorescent Dyes as Tools for Protein Characterization , 2008, Pharmaceutical Research.

[7]  S. Chakrabarti,et al.  Understanding the Genetics of Age-Related Macular Degeneration: Some Insights into the Disease Pathogenesis , 2008 .

[8]  R. Woodworth,et al.  Conalbumin: a rapid, high-yield preparation from egg white. , 1959, Archives of biochemistry and biophysics.

[9]  S. Ventura,et al.  Trifluoroethanol Modulates Amyloid Formation by the All α-Helical URN1 FF Domain , 2013, International journal of molecular sciences.

[10]  A. Donald,et al.  The binding of thioflavin-T to amyloid fibrils: localisation and implications. , 2005, Journal of structural biology.

[11]  C. Ionescu-Zanetti,et al.  Partially folded intermediates as critical precursors of light chain amyloid fibrils and amorphous aggregates. , 2001, Biochemistry.

[12]  T. Kiyono,et al.  Novel anticancer activity of the autocleaved ovotransferrin against human colon and breast cancer cells. , 2009, Journal of agricultural and food chemistry.

[13]  Non-native States of Bovine Beta-Lactoglobulin Induced by Acetonitrile: pH-Dependent Unfolding of the Two Genetic Variants A and B , 2013, Cell Biochemistry and Biophysics.

[14]  A. Soper,et al.  Structural Investigation of Solute−Solute Interactions in Aqueous Solutions of Tertiary Butanol , 1998 .

[15]  L. Stryer,et al.  Fluorescence spectroscopy of proteins. , 1968, Science.

[16]  G. Erf,et al.  Serum ovotransferrin as a biomarker of inflammatory diseases in chickens. , 2009, Poultry science.

[17]  Francesc X. Avilés,et al.  AGGRESCAN: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptides , 2007, BMC Bioinform..

[18]  R. Warner,et al.  The preparation of crystalline conalbumin. , 1951, The Journal of biological chemistry.

[19]  I. Laczkó,et al.  The formation of amyloid-like fibrils of α-chymotrypsin in different aqueous organic solvents. , 2012, Protein and peptide letters.

[20]  A. C. Eissens,et al.  Solid dispersions based on inulin for the stabilisation and formulation of delta 9-tetrahydrocannabinol. , 2004, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[21]  R. Ellis,et al.  Medicine: Danger — misfolding proteins , 2002, Nature.

[22]  I. Wakabayashi,et al.  Sensitivity of thrombin-induced platelet aggregation to inhibition by ethanol. , 2009, Clinica chimica acta; international journal of clinical chemistry.

[23]  N. Inestrosa,et al.  Thioflavin T Is a Fluorescent Probe of the Acetylcholinesterase Peripheral Site That Reveals Conformational Interactions between the Peripheral and Acylation Sites* , 2001, The Journal of Biological Chemistry.

[24]  I. Kuznetsova,et al.  Computational study of thioflavin T torsional relaxation in the excited state. , 2007, The journal of physical chemistry. A.

[25]  A. Naeem,et al.  Acetonitrile can promote formation of different structural intermediate states on aggregation pathway of immunoglobulin G from human and bovine. , 2011, International journal of biological macromolecules.

[26]  R. H. Khan,et al.  Cosolvents Induced Unfolding and Aggregation of Keyhole Limpet Hemocyanin , 2013, Cell Biochemistry and Biophysics.

[27]  Molten globule-like state of bovine carbonic anhydrase in the presence of acetonitrile. , 2006, Journal of biochemistry.

[28]  K. Onuma,et al.  Denaturation and aggregation of hen egg lysozyme in aqueous ethanol solution studied by dynamic light scattering. , 2001, Biopolymers.

[29]  M. Picken,et al.  The spectrum of monoclonal immunoglobulin deposition disease associated with immunocytic dyscrasias. , 1989, Seminars in hematology.

[30]  L. Lai,et al.  Formation of amyloid fibrils from fully reduced hen egg white lysozyme , 2004, Protein science : a publication of the Protein Society.

[31]  A. Fink,et al.  Spectral Properties of Thioflavin T and Its Complexes with Amyloid Fibrils , 2003 .

[32]  K. Gekko,et al.  Acetonitrile-protein interactions: amino acid solubility and preferential solvation. , 1998, Biochimica et biophysica acta.

[33]  D. J. Harrington,et al.  The high resolution crystal structure of deoxyhemoglobin S. , 1997, Journal of molecular biology.

[34]  Yongkang Luo,et al.  Conjugation of ovotransferrin with catechin shows improved antioxidant activity. , 2014, Journal of agricultural and food chemistry.

[35]  Stavros J. Hamodrakas,et al.  A Consensus Method for the Prediction of ‘Aggregation-Prone’ Peptides in Globular Proteins , 2013, PloS one.

[36]  C. Dobson The structural basis of protein folding and its links with human disease. , 2001, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[37]  H W Frijlink,et al.  Incorporation of lipophilic drugs in sugar glasses by lyophilization using a mixture of water and tertiary butyl alcohol as solvent. , 2004, Journal of pharmaceutical sciences.

[38]  C. Sánchez-Moreno,et al.  Protective effect of vitamin C against the ethanol mediated toxic effects on human brain glial cells. , 2003, The Journal of nutritional biochemistry.

[39]  J. King,et al.  Contributions of hydrophobic domain interface interactions to the folding and stability of human γD‐crystallin , 2005, Protein science : a publication of the Protein Society.

[40]  Marie-Hélène Dufresne,et al.  A Novel One-Step Drug-Loading Procedure for Water-Soluble Amphiphilic Nanocarriers , 2004, Pharmaceutical Research.

[41]  D. Droz,et al.  Light-chain deposition disease: its relation with AL-type amyloidosis. , 1984, Kidney international.

[42]  Ejaz Ahmad,et al.  Fluoroalcohols-induced modulation and amyloid formation in conalbumin. , 2014, International journal of biological macromolecules.

[43]  A. Vicente,et al.  Thermodynamic studies of partitioning behavior of lysozyme and conalbumin in aqueous two-phase systems. , 2009, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[44]  R. Hodges,et al.  The two‐stranded α‐helical coiled‐coil is an ideal model for studying protein stability and subunit interactions , 1992, Biopolymers.

[45]  R. H. Khan,et al.  Different molten globule-like folding intermediates of hen egg white lysozyme induced by high pH and tertiary butanol. , 2007, Journal of biochemistry.

[46]  V. Uversky,et al.  Conformational transitions provoked by organic solvents in beta-lactoglobulin: can a molten globule like intermediate be induced by the decrease in dielectric constant? , 1997, Folding & design.

[47]  Guifeng Zhang,et al.  PEGylation of proteins in organic solution: a case study for interferon beta-1b. , 2012, Bioconjugate chemistry.

[48]  C. Zeng,et al.  Tea catechins induce the conversion of preformed lysozyme amyloid fibrils to amorphous aggregates. , 2009, Journal of agricultural and food chemistry.

[49]  Christopher G. Adda,et al.  Interaction of the Molecular Chaperone αB-Crystallin with α-Synuclein: Effects on Amyloid Fibril Formation and Chaperone Activity , 2004 .

[50]  R. H. Khan,et al.  2,2,2-Trifluroethanol induces simultaneous increase in alpha-helicity and aggregation in alkaline unfolded state of bovine serum albumin. , 2010, International journal of biological macromolecules.

[51]  S. N. Timasheff,et al.  Interaction of ribonuclease A with aqueous 2-methyl-2,4-pentanediol at pH 5.8. , 1978, Biochemistry.

[52]  H W Frijlink,et al.  Anomalous dissolution behaviour of tablets prepared from sugar glass-based solid dispersions. , 2004, Journal of controlled release : official journal of the Controlled Release Society.

[53]  E. Rimm,et al.  Roles of drinking pattern and type of alcohol consumed in coronary heart disease in men. , 2003, The New England journal of medicine.

[54]  D. Ahn,et al.  An economic and simple purification procedure for the large-scale production of ovotransferrin from egg white. , 2008, Poultry science.

[55]  S. Fatima,et al.  Interactions of thioflavin T with serum albumins: spectroscopic analyses. , 2009, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

[56]  V. Uversky,et al.  Conformational behavior and aggregation of alpha-synuclein in organic solvents: modeling the effects of membranes. , 2003, Biochemistry.

[57]  W. Huff,et al.  Changes in Serum Ovotransferrin Levels in Chickens with Experimentally Induced Inflammation and Diseases , 2002, Avian diseases.

[58]  R. Khodarahmi,et al.  Study of Cosolvent-Induced α-Chymotrypsin Fibrillogenesis: Does Protein Surface Hydrophobicity Trigger Early Stages of Aggregation Reaction? , 2009, The protein journal.

[59]  N. C. Price,et al.  Acetonitrile-induced unfolding of porcine pepsin A: A proposal for a critical role of hydration structures in conformational stability. , 2009, International journal of biological macromolecules.

[60]  Ejaz Ahmad,et al.  pH-Dependent Conformational Transitions in Conalbumin (Ovotransferrin), a Metalloproteinase from Hen Egg White , 2011, Cell Biochemistry and Biophysics.

[61]  K. Namba,et al.  Amyloid protofilament formation of hen egg lysozyme in highly concentrated ethanol solution , 2008, Protein science : a publication of the Protein Society.

[62]  D. V. Vanden Bout,et al.  Near-field scanning optical microscopy measurements of fluorescent molecular probes binding to insulin amyloid fibrils. , 2009, The journal of physical chemistry. B.

[63]  Kyle A. Zingaro,et al.  GroESL overexpression imparts Escherichia coli tolerance to i-, n-, and 2-butanol, 1,2,4-butanetriol and ethanol with complex and unpredictable patterns. , 2013, Metabolic engineering.

[64]  D. Ahn,et al.  Influence of zinc, sodium bicarbonate, and citric acid on the antibacterial activity of ovotransferrin against Escherichia coli O157:H7 and Listeria monocytogenes in model systems and ham. , 2008, Poultry science.

[65]  V. Uversky,et al.  Fluorescence Quantum Yield of Thioflavin T in Rigid Isotropic Solution and Incorporated into the Amyloid Fibrils , 2010, PloS one.

[66]  J. Holger,et al.  Methanol ingestion: prevention of toxic sequelae after massive ingestion. , 2003, The Journal of emergency medicine.

[67]  V. Uversky,et al.  Spectral properties of thioflavin T in solvents with different dielectric properties and in a fibril-incorporated form. , 2007, Journal of proteome research.

[68]  J. Manning,et al.  Properties of a recombinant human hemoglobin double mutant: Sickle hemoglobin with Leu‐88 (β) at the primary aggregation site substituted by Ala , 1994, Protein science : a publication of the Protein Society.