In silico prediction of B cell epitopes of the extracellular domain of insulin-like growth factor-1 receptor
Vahid
Bayrami
Department of Biotechnology, Faculty of Advanced Sciences and Technologies, University of Isfahan, Isfahan, Iran
author
Mehrnaz
Keyhanfar
Department of Biotechnology, Faculty of Advanced Sciences and Technologies, University of Isfahan, Isfahan, Iran
author
Hassan
Mohabatkar
Department of Biotechnology, Faculty of Advanced Sciences and Technologies, University of Isfahan, Isfahan, Iran
author
Manijeh
Mahdavi
Department of Pharmaceutical Biotechnology, Faculty of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran
author
Violaine
Moreau
Centre de Biochimie Structurale, CNRS UMR 5048, UM 1 & 2- INSERM U 1054, 29 rue de Navacelles, 34090, Montpellier, France
author
text
article
2016
eng
The insulin-like growth factor-1 receptor (IGF-1R) is a transmembrane receptor with tyrosine kinase activity. The receptor plays a critical role in cancer. Using monoclonal antibodies (MAbs) against the IGF-1R, typically blocks ligand binding and enhances down-regulation of the cell-surface IGF-1R. Some MAbs such as cixutumumab are under clinical trial investigation. Targeting multiple distinct epitopes on IGF-1R, might be an effective strategy to inhibit IGF-1R pathway in cancer. In this study, new linear B cell epitopes for the extracellular domains of IGF-1R were predicted by in silico methods using a combination of linear B cell epitope prediction web servers such as ABCpred, Bepired, BCPREDs, Bcepred and Elliprro. Moreover, Discotope, B-pred and PEPOP web server tools were employed to predict new conformational B cell epitopes. In contrast to previously reported epitopes from extracellular region of the IGF-1R, we predicted new linear P8: (RQPQDGYLYRHNYCSK) and conformational Pc4: (HYYYAGVCVPACPPNTYRFE), Ppc6: (KMCPSTGKRENNESAPDNDT) and Ppc20: (ANILSAESSDSEFMQEPSGFI) epitopes. These epitopes are useful for further study as peptide antigens to actively immune host animals to develop new MAbs. Furthermore, the epitopes can be used in peptide-based cancer vaccines design.
Molecular Biology Research Communications
Shiraz University Press
2322-181X
5
v.
4
no.
2016
201
214
https://mbrc.shirazu.ac.ir/article_3832_83706b8a3fd0efa02ea5715d2357366e.pdf
dx.doi.org/10.22099/mbrc.2016.3832
Isolation and identification of Legionella spp. from different aquatic sources in south-west of Iran by molecular &culture methods
Mohammad
Tabatabaei
Department of Pathobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran
author
zahra
Hemmati
Department of Pathobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran
author
Maryam-o-sadat
Moezzi
Department of Pathobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran
author
Negar
azimzade
Department of Pathobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran
author
text
article
2016
eng
Legionella pneumophila, the causative agent of Legionnaires’ diseases (LD) is usually transmitted to humans via inhalation of aerosols from contaminated natural and manmade water sources. These organisms may become fatal especially in immunocompromised patients and LD is the one of the important disease from a public health perspective. This survey investigated the frequency of Legionella spp. including L. pneumophila, in some cold and warm water systems in South-West of Iran by culture and PCR methods. Thirty four water samples were collected from diverse water supply systems. After acid and heat treatments of samples, inoculated onto buffered charcoal yeast extract agar. Isolated colonies were confirmed by morphological and biochemical tests. Then the isolates were examined for icmO, sidA and lidA genes by PCR assay. This study showed that frequency of L. pneumophila was 4 by culture and 14 by PCR. PCR method to be efficient and sensitive test for rapid detection of these organisms in environmental water sources. This study emphasizes the need for effective infection control and prevention strategies to minimize the risk from exposure to potential pathogens such as Legionella spp. and to create a safe working environment.
Molecular Biology Research Communications
Shiraz University Press
2322-181X
5
v.
4
no.
2016
215
223
https://mbrc.shirazu.ac.ir/article_3858_b47a7cfffbcd772d816690d39e69035a.pdf
dx.doi.org/10.22099/mbrc.2016.3858
Influence of heparin molecular size on the induction of C-terminal unfolding in β2-microglobulin
Kanon
Fukasawa
Department of Chemistry, Kurume University School of Medicine, Kurume, Fukuoka, Japan
author
Yuichiro
Higashimoto
Department of Chemistry, Kurume University School of Medicine, Kurume, Fukuoka, Japan
author
Yoshihiro
Motomiya
Suiyukai Clinic, Kashihara, Nara, Japan
author
Yoshinori
Uji
Department of Medical Technology and Sciences, School of Health Sciences at Fukuoka, International University of Health and Welfare, Okawa, Fukuoka, Japan
author
Yukio
Ando
Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Honjo, Kumamoto, Japan
author
text
article
2016
eng
Dialysis-related amyloidosis (DRA) is characterized by accumulation of amyloid β2-microglobulin (β2m) in the interstitial matrix. Matrix substances such as heparin have reportedly been strongly implicated in the pathogenesis of dialysis-related amyloidosis. In clinical setting of hemodialysis, two types of heparin, i.e., high and low molecular heparin (H.M.H. and L.M.H.) have been routinely used. Still commonly used is H.M.H., followed by L.M.H. preparations with distinct advantages. Here, we studied that the interaction of native and two amyloidogenic β2m variants: ΔN6β2m and D76N β2m with H.M.H. and L.M.H. We also investigated whether heparin could induce β2m to have an amyloidogenic conformation.Biolayer interferometry revealed that ΔN6β2m had a strong reaction and D76N β2m had a moderate reaction with H.M.H.. Furthermore, H.M.H. induced the C-terminal unfolding in a native β2m. By contrast, L.M.H. showed no reaction even with ΔN6β2m.This study showed firstly a direct binding of β2m with H.M.H.. H.M.H. would provoked a C-terminal unfolding of β2m, which indicated production of an amyloidogenic intermediate, i.e., β2m92-99. In addition, our findings also suggest that L.M.H. may provide beneficial effects against the development of the DRA.
Molecular Biology Research Communications
Shiraz University Press
2322-181X
5
v.
4
no.
2016
225
232
https://mbrc.shirazu.ac.ir/article_3866_e3deb7382c93556b2b8e5e1c43d317e1.pdf
dx.doi.org/10.22099/mbrc.2016.3866
In silico identification of miRNAs and their target genes and analysis of gene co-expression network in saffron (Crocus sativus L.) stigma
Zahra
Zinati
Agroecology Department, College of Agriculture and Natural Resources of Darab, Shiraz University, Iran
author
Roohollah
Shamloo-Dashtpagerdi
Crop Production and Plant Breeding Department, College of Agriculture, Shiraz University, Iran
author
Ali
Behpouri
Agroecology Department, College of Agriculture and Natural Resources of Darab, Shiraz University, Iran
author
text
article
2016
eng
As an aromatic and colorful plant of substantive taste, saffron (Crocus sativus L.) owes such properties of matter to growing class of the secondary metabolites derived from the carotenoids, apocarotenoids. Regarding the critical role of microRNAs in secondary metabolic synthesis and the limited number of identified miRNAs in C. sativus, on the other hand, one may see the point how the characterization of miRNAs along with the corresponding target genes in C. sativus might expand our perspectives on the roles of miRNAs in carotenoid/apocarotenoid biosynthetic pathway. A computational analysis was used to identify miRNAs and their targets using EST (Expressed Sequence Tag) library from mature saffron stigmas. Then, a gene co-expression network was constructed to identify genes which are potentially involved in carotenoid/apocarotenoid biosynthetic pathways. EST analysis led to the identification of two putative miRNAs (miR414 and miR837-5p) along with the corresponding stem-looped precursors. To our knowledge, this is the first report on miR414 and miR837-5p in C. sativus. Co-expression network analysis indicated that miR414 and miR837-5p may play roles in C. sativus metabolic pathways and led to identification of candidate genes including six transcription factors and one protein kinase probably involved in carotenoid/apocarotenoid biosynthetic pathway. Presence of transcription factors, miRNAs and protein kinase in the network indicated multiple layers of regulation in saffron stigma. The candidate genes from this study may help unraveling regulatory networks underlying the carotenoid/apocarotenoid biosynthesis in saffron and designing metabolic engineering for enhanced secondary metabolites.
Molecular Biology Research Communications
Shiraz University Press
2322-181X
5
v.
4
no.
2016
233
246
https://mbrc.shirazu.ac.ir/article_3875_87c248ee1eac36fe4cfcafdd87e2e48d.pdf
dx.doi.org/10.22099/mbrc.2016.3875
Partial and complete microdeletions of Y chromosome in infertile males from South of Iran
Raheleh
Masoudi
Biology Department, College of Sciences, Shiraz University, Shiraz, Iran
author
Liusa
Mazaheri Asadi
Biology Department, College of Sciences, Shiraz University, Shiraz, Iran
author
Shahryar
Khorasani
Biology Department, College of Sciences, Shiraz University, Shiraz, Iran
author
text
article
2016
eng
Y chromosome microdeletions are the second genetic cause of male infertility. The incidence of Y chromosome microdeletions can vary considerably depending on several factors, including patient selection criteria, population composition, and diagnostic protocols. They are associated with spermatogenic failure and lead to azoospermia or oligozoospermia. The advance in assisted reproductive technology and intracytoplasmic sperm injection, and the possibility of genetic defect transmission to the next generation make it necessary to improve our knowledge about the various factors leading to spermatogenic impairment. This study was designed to determine the frequency of microdeletions of Y chromosome in a population from South of Iran. 81 infertile males with non-obstructive azoospermia or oligozoospermia were selected. Multiplex PCR using several STS markers was carried out to detect the complete or partial microdeletions. The frequency of both complete and partial microdeletions in men with azoospermia or severe oligozoospermia was 7.4%. All microdeletions were observed in AZFc region. There was 1.25% complete microdeletions and after excluding complete microdeletions, we detected 5% gr/gr and 1.25% b2/b3 microdeletions. In our control group of fertile males, 4% gr/gr microdeletions was detected while there was no b2/b3 microdeletions. We concluded that there is a low frequency of Y chromosome microdeletions in a population of infertile males from South of Iran. b2/b3 microdeletions was detected only in infertile males and not in the control group. Screening a population with larger sample size is necessary to determine the involvement of this partial microdeletion in infertility of this population.
Molecular Biology Research Communications
Shiraz University Press
2322-181X
5
v.
4
no.
2016
247
255
https://mbrc.shirazu.ac.ir/article_3893_ac453e5eec75fa36e0797d74c9d22839.pdf
dx.doi.org/10.22099/mbrc.2016.3893
Impact of heat shock step on bacterial transformation efficiency
Maral
Rahimzadeh
Department of Nanobiotechnology, School of Biological Sciences, Tarbiat Modares University, Tehran, Iran
author
Majid
Sadeghizadeh
Department of Molecular Genetics, School of Biological Sciences, Tarbiat Modares University, Tehran, Iran
author
Farhood
Najafi
Department of Resin and Additives, Institute for Color Science and Technology, Tehran, Iran
author
Shahriar
Arab
Department of Biophysics, School of Biological Sciences, Tarbiat Modares University, Tehran, Iran
author
Hamid
Mobasheri
Laboratory of Membrane Biophysics, Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran
author
text
article
2016
eng
CaCl2 treatment followed by heat shock is the most common method for artificial transformation. Here, the cells were transformed using CaCl2 treatment either with heat shock (standard protocol) or without heat shock (lab protocol) to comprehend the difference in transformation efficiency. The BL21 strain of Escherichia coli (E. coli) was being susceptible using CaCl2 treatment. Some Cells were kept at -80 oC while the others were kept at 4 ̊C. Afterwards the susceptible cells were transformed using either standard or lab protocol. The transformation efficiency between cells experienced heat shock and those were not influenced by heat shock was almost the same. Moreover, regardless of transformation protocol, the cells kept at 4 ̊C were transformed more efficiently in compared to those were kept at -80 oC.
Molecular Biology Research Communications
Shiraz University Press
2322-181X
5
v.
4
no.
2016
257
261
https://mbrc.shirazu.ac.ir/article_3915_c33553c369e007f356bf1a28e6f7df87.pdf
dx.doi.org/10.22099/mbrc.2016.3915