Peptides 51 (2014) 35–45
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Peptides
jo ur nal homep age: www.elsevier.com/locate/peptides
Review
Scorpion venom peptides with no disulfide bridges: A review
Ammar Almaaytah
a,∗
, Qosay Albalas
b
a
Department of Pharmaceutical Technology, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid, Jordan
b
Department of Medicinal Chemistry and Pharmacognosy, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid, Jordan
a r t i c l e i n f o
Article history:
Received 5 September 2013
Received in revised form 15 October 2013
Accepted 15 October 2013
Available online 31 October 2013
Keywords:
Scorpion
Venom
Non-disulfide-bridged peptides
NDBPs
Antimicrobial
Anticancer
Structural properties
Classification
a b s t r a c t
Scorpion venoms are rich sources of biologically active peptides that are classified into disulfide-bridged
peptides (DBPs) and non-disulfide-bridged peptides (NDBPs). DBPs are the main scorpion venom com-
ponents responsible for the neurotoxic effects observed during scorpion envenomation as they usually
target membrane bound ion channels of excitable and non-excitable cells. Several hundred DBPs have
been identified and functionally characterized in the past two decades. The NDBPs represent a novel
group of molecules that have gained great interest only recently due to their high diversity both in their
primary structures and bioactivities. This review provides an overview of scorpion NDBPs focusing on
their therapeutic applications, modes of discovery, mechanisms of NDBPs genetic diversity and structural
properties. It also provides a simple classification for NDBPs that could be adopted and applied to other
NDBPs identified in future studies.
© 2013 Elsevier Inc. All rights reserved.
Contents
1. Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
2. General methods of scorpion NDBPs discovery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
3. Structural properties of scorpion NDBPs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
4. Therapeutic applications of NDBPs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
4.1. Bradykinin potentiating activities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
4.2. Antibacterial, antifungal and cytolytic activities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
4.3. NDBPs with antimicrobial activity against antibiotic resistant strains of microorganisms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
4.4. Antiviral activity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
4.5. Antimalarial activity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
4.6. Anticancer activity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
4.7. Immune-modulatory activity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
5. Molecular mechanisms for NDBPs diversity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
6. Classification of NDBPs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
1. Introduction
Scorpions are considered to be one of the oldest animals liv-
ing on the planet and their existence dates back to more than
400 million years ago [32]. Scorpions are represented by around
1500 species and they are distributed geographically all over
the world [46]. Scorpions have acquired the ability to defend
∗
Corresponding author. Tel.: +962 795550234; fax: +962 2 7201075.
E-mail address: amalmaaytah@just.edu.jo (A. Almaaytah).
themselves against predators and capture prey through the produc-
tion of toxin loaded venoms that are secreted through specialized
venom glands found at the end of the scorpion telson [57]. During
their long evolutionary existence on this planet accompanied by the
selective pressure applied on these organisms, scorpions managed
to develop series of venom peptides that display diverse biological
activities and pharmacological functions [52]. The scorpion venom
peptides are generally classified into two main groups: the
disulfide-bridged peptides (DBPs) which usually target membrane
bound ion channels [9,10,54] and the non-disulfide-bridged pep-
tides (NDBPs), a smaller group within the scorpion venom peptide
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