Assays for Light Chain Amyloidosis Formation and Cytotoxicity.
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Luis M Blancas-Mejia | Pinaki Misra | Christopher J Dick | Marta Marin-Argany | Keely R Redhage | Shawna A Cooper | Marina Ramirez-Alvarado | M. Ramirez-Alvarado | L. Blancas-Mejia | Shawna A. Cooper | C. Dick | S. A. Cooper | Marta Marin-Argany | Pinaki Misra | Keely R. Redhage | L. Blancas-Mejía
[1] M. Hosokawa,et al. Fluorometric determination of amyloid fibrils in vitro using the fluorescent dye, thioflavin T1. , 1989, Analytical biochemistry.
[2] P. Hari,et al. Human microvascular dysfunction and apoptotic injury induced by AL amyloidosis light chain proteins. , 2011, American journal of physiology. Heart and circulatory physiology.
[3] M. Wright. Nanoparticle tracking analysis for the multiparameter characterization and counting of nanoparticle suspensions. , 2012, Methods in molecular biology.
[4] C. Murphy,et al. In vitro immunoglobulin light chain fibrillogenesis. , 1999, Methods in enzymology.
[5] R. Falk,et al. Human amyloidogenic light chain proteins result in cardiac dysfunction, cell death, and early mortality in zebrafish. , 2013, American journal of physiology. Heart and circulatory physiology.
[6] R. Wetzel,et al. Kinetics and thermodynamics of amyloid assembly using a high-performance liquid chromatography-based sedimentation assay. , 2006, Methods in enzymology.
[7] R. Falk,et al. Amyloidogenic light chains induce cardiomyocyte contractile dysfunction and apoptosis via a non-canonical p38α MAPK pathway , 2010, Proceedings of the National Academy of Sciences.
[8] H. Levine,et al. Thioflavine T interaction with synthetic Alzheimer's disease β‐amyloid peptides: Detection of amyloid aggregation in solution , 1993, Protein science : a publication of the Protein Society.
[9] F. Ferrone,et al. Analysis of protein aggregation kinetics. , 1999, Methods in enzymology.
[10] L. Serpell,et al. The protofilament substructure of amyloid fibrils. , 2000, Journal of molecular biology.
[11] V. Manganelli,et al. Analyzing morphological and ultrastructural features in cell death. , 2008, Methods in enzymology.
[12] Michele Vendruscolo,et al. Molecular mechanisms of protein aggregation from global fitting of kinetic models , 2016, Nature Protocols.
[13] J. Gross,et al. Nanoparticle tracking analysis of particle size and concentration detection in suspensions of polymer and protein samples: Influence of experimental and data evaluation parameters. , 2016, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[14] S. Kain,et al. Fluorometric and colorimetric detection of caspase activity associated with apoptosis. , 1997, Analytical biochemistry.
[15] Vassar Ps,et al. Fluorescent stains, with special reference to amyloid and connective tissues. , 1959 .
[16] M. Biancalana,et al. Molecular mechanism of Thioflavin-T binding to amyloid fibrils. , 2010, Biochimica et biophysica acta.
[17] M. Ramirez-Alvarado,et al. Recruitment of Light Chains by Homologous and Heterologous Fibrils Shows Distinctive Kinetic and Conformational Specificity. , 2016, Biochemistry.
[18] D. Otzen,et al. ThT 101: a primer on the use of thioflavin T to investigate amyloid formation , 2017, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.
[19] Michele Vendruscolo,et al. Kinetic analysis reveals the diversity of microscopic mechanisms through which molecular chaperones suppress amyloid formation , 2016, Nature Communications.
[20] B. Volkman,et al. Tyrosine Residues Mediate Fibril Formation in a Dynamic Light Chain Dimer Interface , 2012, The Journal of Biological Chemistry.
[21] C. Sigurdson,et al. A Palette of Fluorescent Thiophene-Based Ligands for the Identification of Protein Aggregates , 2015, Chemistry.
[22] S. Latt,et al. Spectral studies on 33258 Hoechst and related bisbenzimidazole dyes useful for fluorescent detection of deoxyribonucleic acid synthesis. , 1976, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[23] I. Johnson,et al. The molecular probes handbook : a guide to fluorescent probes and labeling technologies , 2010 .
[24] D. Teplow,et al. Monitoring protein assembly using quasielastic light scattering spectroscopy. , 1999, Methods in enzymology.
[25] M. Ramirez-Alvarado,et al. Salts enhance both protein stability and amyloid formation of an immunoglobulin light chain. , 2008, Biophysical chemistry.
[26] M. Ramirez-Alvarado,et al. Structural alterations within native amyloidogenic immunoglobulin light chains. , 2009, Journal of molecular biology.
[27] M. Ramirez-Alvarado,et al. Differential Effects on Light Chain Amyloid Formation Depend on Mutations and Type of Glycosaminoglycans* , 2014, Journal of Biological Chemistry.
[28] I. Ermolina,et al. Effect of acidic and basic pH on Thioflavin T absorbance and fluorescence , 2015, European Biophysics Journal.
[29] M. Ramirez-Alvarado,et al. Kinetic control in protein folding for light chain amyloidosis and the differential effects of somatic mutations. , 2014, Journal of molecular biology.
[30] M. Groenning,et al. Binding mode of Thioflavin T and other molecular probes in the context of amyloid fibrils—current status , 2010, Journal of chemical biology.
[31] Y. S. Lubbersen,et al. Thioflavin T fluorescence assay for beta-lactoglobulin fibrils hindered by DAPH. , 2009, Journal of structural biology.
[32] Tuomas P. J. Knowles,et al. The amyloid state and its association with protein misfolding diseases , 2014, Nature Reviews Molecular Cell Biology.
[33] C. Ionescu-Zanetti,et al. Mechanism of thioflavin T binding to amyloid fibrils. , 2005, Journal of structural biology.
[34] M. Kumbhakar,et al. Ultrafast bond twisting dynamics in amyloid fibril sensor. , 2010, The journal of physical chemistry. B.
[35] D. Agrawal,et al. Morphological and biochemical characterization and analysis of apoptosis. , 1997, Journal of pharmacological and toxicological methods.
[36] A. Wyllie,et al. Apoptosis: A Basic Biological Phenomenon with Wide-ranging Implications in Tissue Kinetics , 1972, British Journal of Cancer.
[37] H. Levine. Quantification of beta-sheet amyloid fibril structures with thioflavin T. , 1999, Methods in enzymology.
[38] J. Enghild,et al. How Glycosaminoglycans Promote Fibrillation of Salmon Calcitonin* , 2016, The Journal of Biological Chemistry.
[39] A. Wyllie,et al. Cell death: the significance of apoptosis. , 1980, International review of cytology.
[40] N. Davidson,et al. Specific proteolytic cleavage of poly(ADP-ribose) polymerase: an early marker of chemotherapy-induced apoptosis. , 1993, Cancer research.
[41] M. Ramirez-Alvarado,et al. Cell Damage in Light Chain Amyloidosis , 2016, The Journal of Biological Chemistry.
[42] S. Ben‐Sasson,et al. Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation , 1992, The Journal of cell biology.
[43] B. Volkman,et al. Altered Dimer Interface Decreases Stability in an Amyloidogenic Protein* , 2008, Journal of Biological Chemistry.
[44] M. Leone,et al. Thioflavin T hydroxylation at basic pH and its effect on amyloid fibril detection. , 2008, The journal of physical chemistry. B.
[45] C. Reutelingsperger,et al. Expression on B Cells Undergoing Apoptosis Annexin V for Flow Cytometric Detection of Phosphatidylserine , 2022 .
[46] L. Sikkink,et al. Cytotoxicity of amyloidogenic immunoglobulin light chains in cell culture , 2010, Cell Death and Disease.
[47] Mathias Jucker,et al. The Amyloid State of Proteins in Human Diseases , 2012, Cell.
[48] M. Fändrich. On the structural definition of amyloid fibrils and other polypeptide aggregates , 2007, Cellular and Molecular Life Sciences.