Thermal shift assays of marine-derived fungal metabolites from Aspergillus fischeri MMERU 23 against Leishmania major pteridine reductase 1 and molecular dynamics studies

Author(s):  
Harol R. Arias Cardona ◽  
Thamires Q. Froes ◽  
Bruno C. De Souza ◽  
Franco H. A. Leite ◽  
Hugo Neves Brandão ◽  
...  
2016 ◽  
Vol 110 (3) ◽  
pp. 42a
Author(s):  
Scott A. Hollingsworth ◽  
James B. Fields ◽  
Georges Chreifi ◽  
Matthias Heyden ◽  
Anton P. Arce ◽  
...  

Biochemistry ◽  
2015 ◽  
Vol 54 (49) ◽  
pp. 7272-7282 ◽  
Author(s):  
James B. Fields ◽  
Scott A. Hollingsworth ◽  
Georges Chreifi ◽  
Matthias Heyden ◽  
Anton P. Arce ◽  
...  

2018 ◽  
Vol 24 (11) ◽  
Author(s):  
Larissa de Mattos Oliveira ◽  
Janay Stefany Carneiro Araújo ◽  
David Bacelar Costa Junior ◽  
Isis Bugia Santana ◽  
Angelo Amâncio Duarte ◽  
...  

2020 ◽  
Vol 117 (46) ◽  
pp. 28971-28979
Author(s):  
Sakshi Gera ◽  
Damini Sant ◽  
Shozeb Haider ◽  
Funda Korkmaz ◽  
Tan-Chun Kuo ◽  
...  

Blocking the action of FSH genetically or pharmacologically in mice reduces body fat, lowers serum cholesterol, and increases bone mass, making an anti-FSH agent a potential therapeutic for three global epidemics: obesity, osteoporosis, and hypercholesterolemia. Here, we report the generation, structure, and function of a first-in-class, fully humanized, epitope-specific FSH blocking antibody with aKDof 7 nM. Protein thermal shift, molecular dynamics, and fine mapping of the FSH–FSH receptor interface confirm stable binding of the Fab domain to two of five receptor-interacting residues of the FSHβ subunit, which is sufficient to block its interaction with the FSH receptor. In doing so, the humanized antibody profoundly inhibited FSH action in cell-based assays, a prelude to further preclinical and clinical testing.


2006 ◽  
Vol 64 (2) ◽  
pp. 385-390 ◽  
Author(s):  
Gianluca Bianchini ◽  
Alessio Bocedi ◽  
Paolo Ascenzi ◽  
Enrico Gavuzzo ◽  
Fernando Mazza ◽  
...  

Author(s):  
Ann LeFurgey ◽  
Peter Ingram ◽  
J.J. Blum ◽  
M.C. Carney ◽  
L.A. Hawkey ◽  
...  

Subcellular compartments commonly identified and analyzed by high resolution electron probe x-ray microanalysis (EPXMA) include mitochondria, cytoplasm and endoplasmic or sarcoplasmic reticulum. These organelles and cell regions are of primary importance in regulation of cell ionic homeostasis. Correlative structural-functional studies, based on the static probe method of EPXMA combined with biochemical and electrophysiological techniques, have focused on the role of these organelles, for example, in maintaining cell calcium homeostasis or in control of excitation-contraction coupling. New methods of real time quantitative x-ray imaging permit simultaneous examination of multiple cell compartments, especially those areas for which both membrane transport properties and element content are less well defined, e.g. nuclei including euchromatin and heterochromatin, lysosomes, mucous granules, storage vacuoles, microvilli. Investigations currently in progress have examined the role of Zn-containing polyphosphate vacuoles in the metabolism of Leishmania major, the distribution of Na, K, S and other elements during anoxia in kidney cell nuclel and lysosomes; the content and distribution of S and Ca in mucous granules of cystic fibrosis (CF) nasal epithelia; the uptake of cationic probes by mltochondria in cultured heart ceils; and the junctional sarcoplasmic retlculum (JSR) in frog skeletal muscle.


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