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1.
Indian J Biochem Biophys ; 2010 Apr; 47(2): 67-74
Article in English | IMSEAR | ID: sea-135246

ABSTRACT

The heme-regulated inhibitor (HRI), a member of the eIF-2 kinase family is crucial for regulating protein synthesis during stress. In addition to heme, stress proteins Hsp90 and Hsp70 are known to regulate HRI. The present study aims to determine the physical association of these Hsps in the regulation of HRI activation during oxidative stress using human K562 cells as a model. Extracts from the stress-induced cells were used for determining HRI kinase activity by measuring eIF-2 phosphorylation, and Hsp-HRI interaction by immunoprecipitation and immunoblot analyses. The results indicate a significant increase in both Hsp70 and Hsp90 expression during AAPH (2, 2’-azobis (2-amidinopropane) dihydrochloride)-induced oxidative stress. Further, their interaction with HRI, which correlates well with its increased HRI kinase activity leads to inhibition of protein synthesis. Thus, we demonstrate that Hsps play an important role in the regulation of initiation of protein synthesis during oxidative stress.


Subject(s)
Amidines/chemistry , Amidines/pharmacology , Animals , Enzyme Activation/drug effects , HSP70 Heat-Shock Proteins/metabolism , HSP90 Heat-Shock Proteins/metabolism , Hemin/pharmacology , Humans , Hydrophobic and Hydrophilic Interactions , Intracellular Space/drug effects , Intracellular Space/metabolism , K562 Cells , Oxidative Stress/drug effects , Phosphorylation/drug effects , Protein Biosynthesis/drug effects , Reactive Oxygen Species/metabolism
2.
Southeast Asian J Trop Med Public Health ; 2005 Sep; 36(5): 1139-44
Article in English | IMSEAR | ID: sea-30569

ABSTRACT

Two major factors, higher temperatures and the application of insecticides, can drastically alter the genetic structure of a vector mosquito population. Due to these two stresses, the majority of the population gets wiped out, but the ones that withstand the stress and survive are likely to pass on survivability, and have an altered physiology. Our study shows that exposures to higher temperatures and DDT during the larval stage affects their susceptibility as adult mosquitoes to the DEN-2 virus. The overall transcription and translation status of heat shock protein (Hsp70) in virus high- and low-susceptible was the same as that in other batches. In the case of a DDT-resistant (R-7) strain two bands were obtained during RT-PCRs after heat shock. These two alleles were obtained only with HY-1 in which R-7 males were used for the crosses, suggesting that the second allele is probably male sex linked. The higher expression of Hsp70 may provide DDT-resistant strains a better chance of survival high temperature environments, particularly in homozygotes and hybrids. It was also interesting to note that these strains have a significantly lower susceptibility to the virus. Wide-spread DDT-resistance and a rise in temperature above the average temperature during summer may result in a population with a low susceptibility to the virus. Several families of heat shock proteins are known to be expressed in mosquitoes, and may have a cumulative role in determining susceptibility to the virus, which itself is governed by several genes.


Subject(s)
Animals , Blotting, Western , Culicidae/genetics , DDT , Dengue Virus/genetics , Genetic Predisposition to Disease , India , Insecticide Resistance , Larva/drug effects , Male , Mosquito Control , Temperature
3.
J Biosci ; 2001 Jun; 26(2): 225-31
Article in English | IMSEAR | ID: sea-110866

ABSTRACT

Leishmania donovani requires an exogenous source of heme for growth and transformation. In in vitro culture of the free-living promastigotes, exogenously added hemin enhances cell proliferation. In this investigation, the question of the function of heme with particular reference to protein synthesis and cell proliferation has been addressed. The results of in vitro cell culture experiments demonstrated that hemin (10 microM) alone is suitable for supporting optimum level of protein synthesis, and thereby cell proliferation of promastigotes to an extent that it can replace fetal bovine serum. However, in situ labelling experiments along with Western blots revealed that high concentration of hemin (50 microM) reduced the level of protein synthesis in general and of beta-tubulin in particular with a concomitant induction of hsp90, and induced consequent morphological changes that are observed during in situ transformation of promastigotes in mammalian macrophages. These results therefore suggest that sudden exposure to high concentration of heme in mammalian macrophages may be one of the key factors that trigger promastigote to amastigote transformation in L. donovani. Furthermore, hemin with its dual characteristic could be used as a tool to understand molecular mechanism of cell proliferation and transformation in these parasites.


Subject(s)
Animals , Cell Division/drug effects , Dose-Response Relationship, Drug , HSP90 Heat-Shock Proteins/biosynthesis , Hemin/pharmacology , Immunoblotting , Leishmania donovani/cytology , Protein Biosynthesis/drug effects , Protozoan Proteins/biosynthesis , Tubulin/biosynthesis
4.
Indian J Exp Biol ; 2001 Jan; 39(1): 95-7
Article in English | IMSEAR | ID: sea-60278

ABSTRACT

A simple and one-step detergent-mediated destaining procedure for SDS Polyacrylamide gels for proteins is described. Suspension (5%, w/v) of a commercially available household detergent, Vim Ultra, has been found to be very efficient in destaining polyacrylamide gels without interfering with the resolution of proteins. As compared to the routinely used solvent (methanol-acetic acid-water)-mediated destaining procedure, the present method is economical and user-friendly.


Subject(s)
Detergents/chemistry , Electrophoresis, Polyacrylamide Gel/methods , Indicators and Reagents/chemistry , Rosaniline Dyes/chemistry
5.
J Biosci ; 1997 Jun; 22(3): 287-298
Article in English | IMSEAR | ID: sea-161117

ABSTRACT

The heme regulated eukaryotic initiation factor 2α (eIF 2α) kinase, also called the heme regulated inhibitor (HRI), is a key regulator of protein synthesis in mammalian reticulocyte. HRI is almost undetectable in blood samples of normal rabbits and it increases by 12 15 fold in the reticulocytes of anemic rabbits. In order to determine if such an increase in the quantity of HRI is gradual during anemia, and if it could be an indicator of anemia, we have carried out a detailed analysis on the expression of HRI and its eIF 2α kinase activity in rabbit reticulocyte lysates during various stages of acetylphenylhydrazine (APH) induced anemia. In a 9 day schedule of induction of anemia, using an anti HRI monoclonal antibody, HRI was detectable immediately after completion of fourth injection (day 5) and it increased gradually during the entire period reaching its maximum (24 fold) on day 9. Furthermore, when rabbits recovered from anemia due to individual response to the drug, quantity of HRI decreased significantly. Northern blot analysis results were similar to those of the Western blot. The other parameters that are generally used to monitor anemia in human patients, namely, reticulocyte count, haematocrit level and haemoglobin content although changed at the onset of anemia, did not change significantly during its progression. These results thus indicate that HRI could be a more appropriate and sensitive indicator of drug induced anemia.

6.
J Biosci ; 1996 Apr; 21(2): 191-205
Article in English | IMSEAR | ID: sea-161034

ABSTRACT

Among the various heat shock proteins (HSPs), members of the HSP70 and HSP90 families have drawn particular attention due to their heat shock-unrelated functions. HSP90, an ubiquitous and abundant member of the HSP90 family has been shown to be associated with a large array of protein factors. These proteins reside in the nucleus as well as in the cytoplasm and are involved in various physiological processes, such as, regulation of chromatin structure, cell cycle, cytoskelelal architecture, protein trafficking and protein synthesis. In this article, we focus our interest on the role of HSP90 in protein synthesis. Recent data obtained from a few laboratories strongly suggest that HSP90 interacts with the heme-regulated eukaryotic initiation factor 2α (elF-2α) kinase, also called the heme-regulated inhibitor, and causes its activation which leads to inhibition of protein synthesis. On the basis of data reported from various laboratories, including our own, we propose a possible model on the mechanism of HSP90- mediated activation of heme-regulated inhibitor and regulation of protein synthesis.

7.
Indian J Biochem Biophys ; 1995 Feb; 32(1): 21-31
Article in English | IMSEAR | ID: sea-28913

ABSTRACT

Antisera prepared against total water-soluble lens proteins of the shark, Scoliodon sorrakowah were reacted with homologous antigen and analysed reaction products by immunoelectrophoresis (IE) and two dimensional crossed antigen-antibody electrophoresis (2D-CE). On IE, shark antigens formed 5 precipitin lines including 1 alpha, 3 beta and 1 gamma crystallins and on 2D-CE 3 alpha, 6 beta and 6 gamma peaks accounting for 8%, 27% and 65% antigen in the respective group were obtained from the total crystallins. Using anti-shark antisera, the immunocrossreactivity of lens proteins from 6 Chondropterygii, 23 teleosts and 16 higher vertebrates was examined by IE. It is found that beta crystallins are the most conserved and crossreact with all vertebrate classes, whereas gamma crystallin crossreactivity is specific to the class Pisces and alpha crystallins are least conserved and their crossreactivity is confined to subclass Chondropterygii. Based on IE patterns, a phylogenetic tree is constructed which demonstrates the intrafamily closeness except in case of adaptive radiation.


Subject(s)
Animals , Antigen-Antibody Reactions , Cross Reactions , Crystallins/immunology , Phylogeny , Sharks/immunology , Vertebrates/immunology
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