Elena V. Protopopova
State Research Center of Virology and Biotechnology VECTOR
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Featured researches published by Elena V. Protopopova.
Archives of Virology | 2009
Galina N. Leonova; Ilia G. Kondratov; Vladimir A. Ternovoi; Elena V. Romanova; Elena V. Protopopova; Eugene V. Chausov; Elena V. Pavlenko; Elena I. Ryabchikova; Sergey I. Belikov; Valery B. Loktev
We report the isolation and detailed characterization of the novel strain, Partizansk/2006, of Powassan virus (POWV) from a human case of infection, which occurred in Primorsky krai, Russia, in 2006. Comparative complete genome sequence analysis of the Far Eastern strains Spassk-9 (1975), Nadezdinsk-1991 and Partizansk/2006 of POWV revealed that these strains are 99.8% similar to the LB strain, which was isolated in Canada in 1958. Phylogenetic analysis of 5′ UTR sequences of five other strains of POWV isolated from 1972 to 1986 in Primorsky krai produced similar results. Presumably, Far Eastern POWV has common putative ancestor with LB strain POWV from North America, and the time of divergence of these POWVs is relatively short. We conclude that POWV has become endemic in Far Eastern Russia.
Biochemistry | 2010
M. V. Bogachek; Boris N. Zaitsev; S. K. Sekatskii; Elena V. Protopopova; Vladimir A. Ternovoi; A. V. Ivanova; A. V. Kachko; V. A. Ivanisenko; Giovanni Dietler; Valery B. Loktev
Recombinant polypeptide containing the 260–466 amino acid sequence of West Nile virus (WNV) strain LEIV-Vlg99-27889-human glycoprotein E (gpE, E260–466) was constructed. Immunochemical similarity between the E260–466 and gpE of WNV was proven by enzyme immunoassay (EIA), immunoblot, competitive EIA, hemagglutination inhibition, and neutralization tests using polyclonal and monoclonal antibodies against the viral gpE and recombinant E260–466. Polypeptide E260–466 induced formation of virus neutralizing and cross-reactive antibodies that were interactive with various epitopes of this recombinant protein. It is shown by evaluation of the interaction of E260–466 with one of the proposed cell receptors of WNV that average E260–466-αVβ3 integrin-specific interaction force measured using atomic force spectroscopy was 80 and 140 pN for single and double interactions, correspondingly. Taken together with previously described interaction between laminin-binding protein (LBP) and WNV gpE domain II, it is proposed that WNV gpE can interact specifically with two cellular proteins (LBP and αVβ3 integrin) during virus entry.
Emerging Infectious Diseases | 2007
Vladimir A. Ternovoi; Elena V. Protopopova; Eugene V. Chausov; Dmitry V. Novikov; Galina N. Leonova; Sergey V. Netesov; Valery B. Loktev
We isolated a novel strain of tickborne encephalitis virus (TBEV), Glubinnoe/2004, from a patient with a fatal case in Russia. We sequenced the strain, whose landmark features included 57 amino acid substitutions and 5 modified cleavage sites. Phylogenetically, Glubinnoe/2004 is a novel variant that belongs to the Eastern type of TBEV.
Journal of Molecular Recognition | 2014
Boris N. Zaitsev; Fabrizio Benedetti; Andrey Mikhaylov; Denis V. Korneev; S. K. Sekatskii; Tanya Karakouz; Pavel A. Belavin; Nina A. Netesova; Elena V. Protopopova; Svetlana N. Konovalova; Giovanni Dietler; Valery B. Loktev
The specific interactions of the pairs laminin binding protein (LBP)–purified tick‐borne encephalitis viral surface protein E and certain recombinant fragments of this protein, as well as West Nile viral surface protein E and certain recombinant fragments of that protein, are studied by combined methods of single‐molecule dynamic force spectroscopy (SMDFS), enzyme immunoassay and optical surface waves‐based biosensor measurements. The experiments were performed at neutral pH (7.4) and acid pH (5.3) conditions. The data obtained confirm the role of LBP as a cell receptor for two typical viral species of the Flavivirus genus. A comparison of these data with similar data obtained for another cell receptor of this family, namely human αVβ3 integrin, reveals that both these receptors are very important. Studying the specific interaction between the cell receptors in question and specially prepared monoclonal antibodies against them, we could show that both interaction sites involved in the process of virus–cell interaction remain intact at pH 5.3. At the same time, for these acid conditions characteristic for an endosome during flavivirus–cell membrane fusion, SMDFS data reveal the existence of a force‐induced (effective already for forces as small as 30–70 pN) sharp globule–coil transition for LBP and LBP–fragments of protein E complexes. We argue that this conformational transformation, being an analog of abrupt first‐order phase transition and having similarity with the famous Rayleigh hydrodynamic instability, might be indispensable for the flavivirus–cell membrane fusion process. Copyright
Zentralblatt Fur Bakteriologie-international Journal of Medical Microbiology Virology Parasitology and Infectious Diseases | 1999
Elena V. Protopopova; Aleksandr V. Sorokin; Svetlana N. Konovalova; Alla V. Kachko; Sergey V. Netesov; Valery B. Loktev
Summary We propose an approach to obtain the cell receptor for the tick-borne encephalitis (TBE) virus by affinity chromatography using polyclonal antiidiotyping antibodies (AlAbs) as antireceptor antibodies. The purified fraction of the cell receptor contains four polypeptides with molecular weights of 43, 67, 110, and 210 kDa. Polyclonal AlAbs interacted only with the 67 kDa protein in immunoblotting. The molecular size of the 67 kDa protein suggested that it is the nonintegrin laminin binding protein (LBP). Using the polymerase chain reaction and appropriate primers, the amplified fragments, containing the gene of the human laminin binding protein, were cloned from the RH cells; a gene-engineering product of the recombinant laminin binding protein was developed. The highly purified recombinant LBP interacted with the native protein E of the TBE virus and also competed with monoclonal antibody for interaction with protein E. The affinity of the interaction of the recLBP with protein E of the TBE virus was estimated to be 0.5–5 x 10 7 M ‡1 .
Mitochondrial DNA | 2016
Tamara P. Mikryukova; Vladimir N. Romanenko; Evgene V. Chausov; Svetlana N. Konovalova; Vladimir A. Ternovoi; Elena V. Protopopova; Yulia V. Kononova; Igor G. Korobitsyn; N. S. Moskvitina; Valery B. Loktev
Abstract Here, we present complete mitochondrial DNA sequence of Ixodes pavlovskyi Pom., 1946 for the first time. The mitogenome is 14,575 bp in length and contains 13 protein-coding genes, 2 rRNA genes, 22 tRNA genes and a control region. The overall base composition is 40.1% T, 13.8% C, 37.9% A and 8.1% G. Four protein-coding genes are initiated by ATT codon, three genes – by ATA codon and ATG start codon is found for six genes. Only tRNA-Lys, tRNA-Ile, tRNA-Arg are folded into the cloverleaf secondary structure, other tRNA have atypical structure with reduced T- or D-arms.
Biology Bulletin | 2014
N. S. Moskvitina; Igor G. Korobitsyn; O. Yu. Tyuten’kov; Sergey Gashkov; Yu. V. Kononova; S. S. Moskvitin; Vladimir N. Romanenko; T. P. Mikryukova; Elena V. Protopopova; M. Yu. Kartashov; E. V. Chausov; Svetlana N. Konovalova; N. L. Tupota; A. O. Sementsova; Vladimir A. Ternovoi; V. B. Loktev
The role of birds in the focus of tick-borne infections was studied from 2006 to 2011. The frequency index of ticks carried by ground dwelling birds is about 49.7%. The index of their abundance is 3.8. The larvae of ticks have been found on birds in 43.8% of cases. Nymphs and adult ticks have been found in 39.9 and 16.3%, respectively. It was revealed that Ixodex pavlovskyi was transferred and dominated in the urban microfoci because of its ornithophily. The markers of infectious agents have been recorded in 42 of 60 bird species under study.
Tsitologiia | 2007
M. M. Gridina; Elena V. Protopopova; A. V. Kachko; Alla V. Ivanova; E. I. Bondarenko; Valery B. Loktev
The expression of the laminin-binding protein (LBP) on cellular membranes in different cell lines has been studied. A high level of replication of Venezuelan equine encephalomyelitis (VEE) virus was registered in Vero cells with high levels of LBP on the cell surface. The treatment of Vero cells with monoclonal antibodies to human LBP reduced VEE virus replication by a factor of more than 200. A low level of LBP expression on the surface of 293 cells was increased via transfection by plasmid with gene for human LBP. The VEE virus replication in transfected cells (9S2) was increased by more that 2000 times compared to the 293 cells. The results demonstrated the principal role of cellular LBP in the entry of VEE virus into mammalian cells. It is proposed that LBP is a key cellular protein for the early stage of the VEE virus replication in cells. LBP may be a target protein for the development of a new generation of antiviral drugs capable of inhibiting (enhancing) the alphavirus replication in human cells.
Vaccine | 2007
Galina N. Leonova; Vladimir A. Ternovoi; Elena V. Pavlenko; Olga S. Maistrovskaya; Elena V. Protopopova; Valery B. Loktev
Ticks and Tick-borne Diseases | 2014
Tamara P. Mikryukova; N. S. Moskvitina; Yulia V. Kononova; Igor G. Korobitsyn; Mikhail Yu. Kartashov; Oleg Y. Tyuten′kov; Elena V. Protopopova; Vladimir N. Romanenko; Evgeny V. Chausov; Sergey Gashkov; Svetlana N. Konovalova; Sergey S. Moskvitin; Natalya L. Tupota; Alexandra O. Sementsova; Vladimir A. Ternovoi; Valery B. Loktev
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State Research Center of Virology and Biotechnology VECTOR
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View shared research outputsState Research Center of Virology and Biotechnology VECTOR
View shared research outputsState Research Center of Virology and Biotechnology VECTOR
View shared research outputsState Research Center of Virology and Biotechnology VECTOR
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