Identification of natural peptides as a new class of antimalarial drugs by in silico approaches

Malaria is one of the most widespread and serious parasitic diseases worldwide. Currently available antimalarial drugs have side effects, and many strains of Plasmodia have developed resistance to such drugs. The present review examines the use of annexins and of natural peptides from snake venom as...

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Main Authors: Samy, R., Foo, S., Franco, O., Stiles, B., Kumar, Alan Prem, Sethi, Gautam, Lim, L.
Format: Journal Article
Published: 2017
Online Access:http://hdl.handle.net/20.500.11937/52001
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author Samy, R.
Foo, S.
Franco, O.
Stiles, B.
Kumar, Alan Prem
Sethi, Gautam
Lim, L.
author_facet Samy, R.
Foo, S.
Franco, O.
Stiles, B.
Kumar, Alan Prem
Sethi, Gautam
Lim, L.
author_sort Samy, R.
building Curtin Institutional Repository
collection Online Access
description Malaria is one of the most widespread and serious parasitic diseases worldwide. Currently available antimalarial drugs have side effects, and many strains of Plasmodia have developed resistance to such drugs. The present review examines the use of annexins and of natural peptides from snake venom as a new class of anti-malarial agents, with the key property of reducing inflammation. Severe cases of malaria manifest elevated serum levels of liver enzymes, inflammation, fibrin deposition, apoptosis, and reduction in peripheral CD8+ T cells. The annexin-A1/5 proteins trigger inflammation via increased expression of diverse cytokines (tumor necrosis factor alpha, interleukin-1beta, interleukin-10), however, by shielding microbial phospholipids they prevent injury via damage-associated molecular patterns (DAMPs). Here, we also review an in silico-based bioengineering approach that may allow for a better design, synthesis and characterization of novel peptides from snake venom as a more effective approach to treatment due to their improved antimalarial activity.
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spelling curtin-20.500.11937-520012017-10-05T05:28:29Z Identification of natural peptides as a new class of antimalarial drugs by in silico approaches Samy, R. Foo, S. Franco, O. Stiles, B. Kumar, Alan Prem Sethi, Gautam Lim, L. Malaria is one of the most widespread and serious parasitic diseases worldwide. Currently available antimalarial drugs have side effects, and many strains of Plasmodia have developed resistance to such drugs. The present review examines the use of annexins and of natural peptides from snake venom as a new class of anti-malarial agents, with the key property of reducing inflammation. Severe cases of malaria manifest elevated serum levels of liver enzymes, inflammation, fibrin deposition, apoptosis, and reduction in peripheral CD8+ T cells. The annexin-A1/5 proteins trigger inflammation via increased expression of diverse cytokines (tumor necrosis factor alpha, interleukin-1beta, interleukin-10), however, by shielding microbial phospholipids they prevent injury via damage-associated molecular patterns (DAMPs). Here, we also review an in silico-based bioengineering approach that may allow for a better design, synthesis and characterization of novel peptides from snake venom as a more effective approach to treatment due to their improved antimalarial activity. 2017 Journal Article http://hdl.handle.net/20.500.11937/52001 10.2741/S475 restricted
spellingShingle Samy, R.
Foo, S.
Franco, O.
Stiles, B.
Kumar, Alan Prem
Sethi, Gautam
Lim, L.
Identification of natural peptides as a new class of antimalarial drugs by in silico approaches
title Identification of natural peptides as a new class of antimalarial drugs by in silico approaches
title_full Identification of natural peptides as a new class of antimalarial drugs by in silico approaches
title_fullStr Identification of natural peptides as a new class of antimalarial drugs by in silico approaches
title_full_unstemmed Identification of natural peptides as a new class of antimalarial drugs by in silico approaches
title_short Identification of natural peptides as a new class of antimalarial drugs by in silico approaches
title_sort identification of natural peptides as a new class of antimalarial drugs by in silico approaches
url http://hdl.handle.net/20.500.11937/52001