Genomic Structure of Two Kv1.3 Channel Blockers from Scorpion Mesobuthus eupeus and Sea Anemone Stichodactyla haddoni and Construction of their Chimeric Peptide as a Novel Blocker

Author(s):  
Maryam Asadi ◽  
Hoda Ayat ◽  
Ali Mohammad Ahadi ◽  
Mohammad Sharif Ranjbar
1979 ◽  
Vol 83 (1) ◽  
pp. 283-292
Author(s):  
ROGER LUBBOCK

The response of nematocytes in the anemone Stichodactyla haddoni to contact with complex organic compounds varies according to the 9ubstance concerned and in most cases according to the level of accompanying mechanical stimulation. Compounds with a proteinaceous moiety differ in their capacity to excite nematocytes, but usually tend to induce a stronger response than polysaccharides or lipids. Nematocyst discharge against foreign animals appears to be the result of a sophisticated cellular recognition process in which the nematocytes, and/or cells closely associated with them, respond to physical contact with a surface of appropriate chemical composition.


Peptides ◽  
2008 ◽  
Vol 29 (4) ◽  
pp. 536-544 ◽  
Author(s):  
Tomohiro Honma ◽  
Shino Kawahata ◽  
Masami Ishida ◽  
Hiroshi Nagai ◽  
Yuji Nagashima ◽  
...  

Author(s):  
Neda Fazeli ◽  
Akram Sadat Naeemi ◽  
Seyed Amir Hossein Jalali ◽  
Hojjatollah Zamani

Background: Staphylococcus aureus and Pseudomonas aeruginosa are important human bacterial pathogens, which are resistant to several antibiotics. One of the main causes of their resistance is the ability of biofilm formation. Objectives: The present study aimed to evaluate the antibacterial and antibiofilm activity of the extracts of Vibrio parahaemolyticus, V. alginolyticus, Pseudoalteromonas gelatinilytica, and Pseudoalteromonas piscicida isolated from sea anemone (Stichodactyla haddoni) against S. aureus and P. aeruginosa. Methods: Four isolated bacteria were identified using biochemical and molecular identification methods, and their extracts were obtained by mixing the cell-free supernatants from their old broth culture using ethyl acetate and methanol as the solvents. The agar well-diffusion and micro-dilution methods were also applied to determine the antibacterial activity, minimum bactericidal concentration (MBC), and minimum inhibitory concentration (MIC) of the extracts. The ability of the extracts to inhibit biofilm formation and disrupt the preformed biofilm of the pathogens was attained through crystal violet staining in 96-well microtiter plates. To determine the nature of the extracts, they were exposed to protease enzyme, and the antibiofilm activity was compared with the untreated extracts. Results: The extracts of the four isolated bacteria inhibited bacterial growth and biofilm formation and disrupted the preformed biofilm of S. aureus (MIC = BIC = 600 µg/mL) and P. aeruginosa (MIC = BIC = 300 µg/mL). In addition, the active compounds of the extracts with antibiofilm activities were mainly proteases. Conclusions: According to the results, V. parahaemolyticus, V. alginolyticus, P. gelatinilytica, and P. piscicida had antibacterial and antibiofilm potential against S. aureus and P. aeruginosa, and their extract could also be further analyzed as an alternative to antibiotics.


2014 ◽  
Vol 8 ◽  
pp. BBI.S13403 ◽  
Author(s):  
Angélica Sabogal-Arango ◽  
George E. Barreto ◽  
David Ramírez-Sánchez ◽  
Juan González-Mendoza ◽  
Viviana Barreto ◽  
...  

Sea anemone neurotoxins are peptides that interact with Na+ and K+ channels, resulting in specific alterations on their functions. Some of these neurotoxins (1ROO, 1BGK, 2K9E, 1BEI) are important for the treatment of about 80 autoimmune disorders because of their specificity for Kv1.3 channel. The aim of this study was to identify the common residues among these neurotoxins by computational methods, and establish whether there is a pattern useful for the future generation of a treatment for autoimmune diseases. Our results showed eight new key common residues between the studied neurotoxins interacting with a histidine ring and the selectivity filter of the receptor, thus showing a possible pattern of interaction. This knowledge may serve as an input for the design of more promising drugs for autoimmune treatments.


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