Skip to main content

Quantification of Soluble or Insoluble Fractions of Leishmania Parasite Proteins in Microvolume Applications: A Simplification to Standard Lowry Assay.

Protein quantification is often an important step in the field of research involving protein. Although the standard Lowry assay and the most abundant modifications used in quantifying protein, the method that is rigid or often exhibit non-linear between protein concentration and color intensity.

 A fast and accurate method for qualitative Porcine Recombinant Proteins and / or quantitative determination of the amount of protein that is soluble / insoluble or micro-well plate immobilized protein isolated from the parasite Leishmania in microvolumes described in this study. Improvements in cost-effective techniques necessary to enhance the research output in resource-limited settings. 

This method is a modification to the Lowry assay was established for quantification of the protein. The concentration of unknown samples is calculated using a standard curve prepared using a standard series of bovine serum albumin (BSA). optimized reagent is 2 N NaOH (sodium hydroxide), 2% Na2CO3 (sodium carbonate), 1% CuSO4 (copper sulfate), 2% KNaC4H4O6 (potassium sodium tartrate), and 2 N Folin and Ciocalteu's phenol. 

These modified proteins sensitive test to measure the Leishmania protein in the crude extract totally or partially dissolve in the estimated range of 10-500 mg / ml (1-50 mg / test) and showed linearity between the color intensity and the protein concentration. It is easier, faster method, and accurate way to measure proteins with microvolumes with cost-effective way for routine use in research laboratories in resource-limited settings.
Quantification of Soluble or Insoluble Fractions of Leishmania Parasite Proteins in Microvolume Applications: A Simplification to Standard Lowry Assay.

ISP-RAAC: identification of secretory proteins of the malaria parasite uses reduced amino acid composition.


As the malaria pathogen, parasite malaria secrete a variety of proteins for growth and reproduction.The identification of secretory proteins of the malaria parasite has important reference significance for anti-malaria vaccine development and medicine.In this study, computational classification method developed to identify proteins secreted from Plasmodium. 

Amino acid composition, the composition of the dipeptide and tripeptide composition and reduce amino acid alphabet proposed to illuminate protein sequences, we are more used SVM to train and predict each and optimized features.74 type Rabbit Recombinant Proteins of amino acid decreases the alphabet are used to predict the secretory proteins, the research results indicates that the enhanced accuracy of 91.67% with a correlation coefficient of 0.84 this Mathew (PKS) with a dipeptide composition, and the highest reaching 92.26% prediction accuracy of selection feature, which shows that our method is reputable and reliable in the field of malaria parasite proteins prediction secreted

Comments

Popular posts from this blog

CCL3/Macrophage Inflammatory Protein-1α Is Dually Involved in Parasite Persistence and Induction of a TNF- and IFNγ-Enriched Inflammatory Milieu in Trypanosoma cruzi-Induced Chronic Cardiomyopathy.

CCL3, member of the CC-chemokine family, has been linked to heart tissue macrophage recruitment and parasite control in mouse acute infection with Trypanosoma cruzi, the causative agent of Chagas disease. Here, we approached CCL3 participation in chronic chagasic cardiomyopathy (CCC), the main clinical forms of Chagas disease . We CCC Rat Recombinant Proteins  induced in C57BL / 6 (ccl3 + / +) and CCL3-deficiency (ccl3 - / -) mice by infection with Colombia Type I strain.  In ccl3 + / + mice, high levels CCL3 mRNA and protein were detected in heart tissue during acute and chronic infections. Survival is not affected by the shortage CCL3. Compared with ccl3 + / +, ccl3 chronically infected - / - mice presented decreased cardiac parasitism and inflammation caused by CD8 + cells and macrophages.  Leukocytosis decreased in infected ccl3 - / - mice, in line with the accumulation of CD8 + T cells with no CCR5 + activated LFA-1 + cells in the spleen. Furthermore, T. cruzi-infect...

Vaccine development against the Taenia solium parasite: the role of recombinant protein expression in Escherichia coli.

Taenia solium is a parasitic zoonosis that causes cysticercosis. This parasite is a major cause of human illness in poor communities where transmitted to humans from pigs which act as intermediate hosts. Vaccination of pigs to prevent the transmission of T. solium to humans is an approach that has been investigated for c ontrolling this disease . General Recombinant Proteins A recombinant vaccine antigens, TSOL18, has been very successful in reducing infection with T. solium pigs in tests of experimental challenges. The vaccine has been proven to remove the natural transmission of T. solium obtained in field trials conducted in Africa. We recently reported that the vaccine was also effective in field trials conducted in Peru.  The TSOL18 recombinant antigen for each of these trials have been produced by expression in Escherichia coli. Here we discuss the research that has been done on TSOL18 antigens and antigens associated with a focus on the preparation of the recombinant TSOL18 ...