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Dive into the research topics where V. K. Novikov is active.

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Featured researches published by V. K. Novikov.


FEBS Letters | 1994

Complete nucleotide sequence and genome organization of a tobamovirus infecting cruciferae plants

Yu. L. Dorokhov; Pavel Ivanov; V. K. Novikov; Alexey A. Agranovsky; S. Yu. Morozov; Vladimir A. Efimov; R. Casper; J.G. Atabekov

Genomic RNA sequence of a tobamovirus infecting cruciferae plants (cr‐TMV) was determined. The RNA is composed of 6312 nucleotides and contains four ORFs encoding the proteins of 122K (ORF1), 178K (ORF2), 29K (ORF3) and 18K (capsid protein, ORF4). ORF4 overlaps ORF3 by 74 nucleotides and the overlapping region can be folded into a stable hairpin structure. The 3′‐terminal region of the cr‐TMV RNA preceding the tRNA‐like structure was shown to form six potentially stable pseudoknots.


Biochemistry | 2009

High-sensitivity express immunochromatographic method for detection of plant infection by tobacco mosaic virus

Yu. F. Drygin; A. N. Blintsov; A.P. Osipov; V. G. Grigorenko; I. P. Andreeva; Alexander I. Uskov; Yu. A. Varitsev; B. V. Anisimov; V. K. Novikov; J.G. Atabekov

A highly sensitive express immunochromatography method for molecular diagnosis of plant virus infections was elaborated on the example of a model object — tobacco mosaic virus (TMV). The analysis time does not exceed 5 min, and the lower limit of TMV detection in non-clarified leaf extract (2–4 ng/ml) is comparable with the sensitivity of the enzyme-linked immunosorbent assay of the virus. A single measurement requires 0.1–0.2 ml tested solution (extract from 10–20 mg of leaf material). The sensitivity of TMV determination in the leaf tissue extract was increased by more than one order of magnitude using signal enhancement by silver and is 0.1 ng/ml. In this case, analysis time did not exceed 25 min. The simplicity of this method makes it especially convenient in express diagnosis of numerous analyzed specimens. The prototype of a diagnostic kit for serial analyses of plant viral infections both in laboratory and field conditions was elaborated.


Journal of Protein Chemistry | 1997

Properties of the Coat Protein of a New Tobacco Mosaic Virus Coat Protein ts-Mutant

E. N. Dobrov; M. M. Abu-Eid; Andrey G. Solovyev; S. V. Kust; V. K. Novikov

Amino acid substitutions in a majority of tobacco mosaic virus (TMV) coat protein (CP) ts-mutants have previously been mapped to the same region of the CP molecule tertiary structure, located at a distance of about 70 Å from TMV virion axis. In the present work some properties of a new TMV CP ts-mutant ts21-66 (two substitutions I21 ⇒ T and D66 ⇒ G, both in the 70-Å region) were studied. Thermal inactivation characteristics, sedimentation properties, circular dichroism spectra, and modification by a lysine-specific reagent, trinitrobenzensulfonic acid, of ts21–66 CP were compared with those of wild-type (U1) TMV CP. It is concluded that the 70-Å region represents the most labile portion of the TMV CP molecule. Partial disordering of this region in the mutant CP at permissive temperatures leads to loss of the capacity to form two-layer aggregates of the cylindrical type, while further disordering induced by mild heating results also in the loss of the ability to form ordered helical aggregates.


FEBS Letters | 2005

Coat proteins of two filamentous plant viruses display NTPase activity in vitro

Daria V. Rakitina; Omar L. Kantidze; A. D. Leshchiner; Andrey G. Solovyev; V. K. Novikov; Sergey Y. Morozov; Natalia O. Kalinina

Coat proteins (CPs) of plant viruses are involved in different stages of the viral life cycle such as virion assembly, replication, movement, vector transmission, and regulation of host defense responses. Here, we report that the CPs of two filamentous RNA viruses, potato virus X (PVX, Potexvirus) and potato virus A (PVA, Potyvirus) exhibit an enzyme activity. The CP isolated from PVX virions possesses ATP‐binding and ATPase activities. Recombinant PVX and PVA CPs produced in Escherichia coli show Mg2+‐dependent ATPase and UTPase activities inhibited by antibodies against virus particles. Deletion of the C‐terminal regions of these proteins diminishes their ATPase activity.


Archive | 2002

Scanning Probe Microscopy Of Biomacromolecules: Nucleic Acids, Proteins And Their Complexes

Olga I. Kiselyova; Marat O. Gallyamov; N. S. Nasikan; Igor V. Yaminsky; O.V. Karpova; V. K. Novikov

After successful imaging of DNA biomacromolecules using scanning probe microscopy (SPM) (Bustamante et al., 1992) much progress was achieved in the visualization of their different morphological features in air and liquid environments: cruciforms, R-loops, etc. SPM gives an opportunity for real-time studies of conformational changes of DNA molecules induced by chemical reagents - formation of torroidal and rod-like structures. Recently, SPM has greatly assisted in the measurements of electrical conductivity of individual DNA molecules (Kasumov et al., 2001). SPM opens new possibilities in the study of single macromolecule micromechanics: rigidity, strength of chemical bond and adhesion.


Phytopathology | 1996

Nucleotide sequence of RNA from the sobemovirus found in infected cocksfoot shows a luteovirus-like arrangement of the putative replicase and protease genes

E. V. Ryabov; A. A. Krutov; V. K. Novikov; O. V. Zheleznikova; S. Yu. Morozov; S. K. Zavriev


Nanomedicine: Nanotechnology, Biology and Medicine | 2007

Atomic force microscopy as a tool of inspection of viral infection

Evgeniy V. Dubrovin; Yuri-F. Drygin; V. K. Novikov; Igor V. Yaminsky


Colloid Journal | 2004

Study of the Peculiarities of Adhesion of Tobacco Mosaic Virus by Atomic Force Microscopy

Evgeniy V. Dubrovin; M. N. Kirikova; V. K. Novikov; Yu. F. Drygin; Igor V. Yaminsky


Proceedings of the USSR Academy of Sciences | 1993

Tobamovirus of the cruciferae family nucleotide-sequences of transport protein, capsid protein cistrones and 3'non-coding region

Yu. L. Dorokhov; P.A. Ivanov; V. K. Novikov; Vladimir A. Efimov; J.G. Atabekov


Archive | 2007

Diagnostic Atomic force microscopy as a tool of inspection of viral infection

Evgeniy V. Dubrovin; V. K. Novikov; Igor V. Yaminsky

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Vladimir A. Efimov

Russian Academy of Sciences

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E. N. Dobrov

Moscow State University

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P.A. Ivanov

Moscow State University

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S. K. Zavriev

Russian Academy of Sciences

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