نتایج جستجو برای: melittin

تعداد نتایج: 867  

Journal: :Molecular cancer therapeutics 2009
Aaron M LeBeau W Nathaniel Brennen Saurabh Aggarwal Samuel R Denmeade

Fibroblast-Activation Protein-α (FAP) is a membrane-bound serine protease that is expressed on the surface of reactive stromal fibroblasts present within the majority of human epithelial tumors but is not expressed by normal tissues. FAP is a postprolyl peptidase that differs from other dipeptidyl prolyl peptidases such as diprolylpeptidase 4 in that it also has gelatinase and collagenase endop...

Journal: :The journal of physical chemistry. B 2013
Sheeba J Irudayam Tobias Pobandt Max L Berkowitz

An important step in a phospholipid membrane pore formation by melittin antimicrobial peptide is a reorientation of the peptide from a surface into a transmembrane conformation. Experiments measure the fraction of peptides in the surface state and the transmembrane state, but no computational study exists that quantifies the free energy curve for the reorientation. In this work we perform umbre...

The current research aimed to quantify melittin (MEL) in Iranian honey bee (Apis mellifera meda) venom. To this end, a liquid chromatography-electrospray ionization-ion trap tandem mass spectrometry (LC-ESI-IT-MS/MS) approach was employed. Melittin is the main toxic peptide of honey bee venom with various biological and pharmacological activities. It was extracted with...

Journal: :General physiology and biophysics 1987
T F Aripov I A Rozenshtein B A Salakhutdinov A A Lev V A Gotlib

The interaction of cytotoxin Vc1 and Vc5 from Central Asian cobra and melittin from the bee venom with multilayer liposomes prepared from dimiristoylphosphatidylcholine with an addition of phosphatidic acid have been studied by the method of differential scanning calorimetry. Incorporation of Vc1, Vc5 and melittin into the lipid resulted in pronounced changes in the thermodynamic properties of ...

2015
Belinda Pastrana-Rios Liliana del Valle Sosa Jorge Santiago

Trifluoroacetic acid (TFA) may be the cause of the bottleneck in high resolution structure determination for protein-peptide complexes. Fragment based drug design often involves the use of synthetic peptides which contain TFA (excipient). Our goal was to explore the effects of this excipient on a model complex: centrin-melittin-TFA. We performed Fourier transform infrared, two-dimensional infra...

Journal: :Journal of Student Research 2023

In today’s society, there are more people dying from breast cancer than ever. fact, it has been projected that 1 in 39 women will die cancer. Over the years, scientists have developed many forms of treatment to help alleviate some symptoms and keep at bay, such as chemotherapy immunotherapy. Recently, however, a discovery made could most efficacy effectiveness against Melittin, cationic peptide...

Journal: :Cancer Nanotechnology 2023

Abstract Background Hepatoma is a serious public health concern. New attempts are urgently needed to solve this problem. Melittin, host defense peptide derived from the venom of honeybees, has noteworthy hemolysis and non-specific cytotoxicity in clinical applications. Here, self-assembly melittin vitamin E-succinic acid-(glutamate) 12 (VG) was fabricated via noncovalent ?-stacking hydrogen bon...

Journal: :Biophysical journal 2000
M Bachar O M Becker

A molecular dynamics simulation of melittin in a hydrated dipalmitoylphosphatidylcholine (DPPC) bilayer was performed. The 19, 000-atom system included a 72-DPPC phospholipid bilayer, a 26-amino acid peptide, and more than 3000 water molecules. The N-terminus of the peptide was protonated and embedded in the membrane in a transbilayer orientation perpendicular to the surface. The simulation res...

Journal: :The Journal of biological chemistry 1993
Z He A K Dunker C R Wesson W R Trumble

Calsequestrin is an intermediate affinity, high capacity Ca(2+)-binding protein found in the lumen of the sarcoplasmic reticulum of both skeletal and cardiac muscle cells. Previous sequence analysis suggested that calsequestrin may contain a hydrophobic binding site for the drug trifluoperazine, a site shared by the calmodulin family and shown to play a role in calmodulin/calmodulin receptor in...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید