Please use this identifier to cite or link to this item:https://hdl.handle.net/20.500.12259/42804
Type of publication: research article
Type of publication (PDB): Straipsnis Clarivate Analytics Web of Science / Article in Clarivate Analytics Web of Science (S1)
Field of Science: Biologija / Biology (N010)
Author(s): Sasnauskas, Kęstutis;Buzaitė, Odeta;Vogel, Frank;Jandrig, Burkhard;Ražanskas, Raimundas;Staniulis, Juozas;Scherneck, Siegfried;Krüger, Detlev H;Ulrich, Rainer
Title: Yeast cells allow high-level expression and formation of polyomavirus-like particles
Is part of: Biological chemistry. Berlyn : Walter de Gruyter GimbH, 1999, vol. 380, iss. 3
Extent: p. 381-386
Date: 1999
Keywords: Gene transfer;Hamster polyomavirus;Nuclear localization signal;Virus-like particles
Abstract: Polyomavirus-derived virus-like particles (VLPs) have been described as potential carriers for encapsidation of nucleic acids in gene therapy. Although VLPs can be generated in E. coli or insect cells, the yeast expression system should be advantageous as it is well established for the biotechnological generation of products for human use, especially because they are free of toxins hazardous for humans. We selected the yeast Saccharomyces cerevisiae for expression of the major capsid protein VP1 of a non-human polyomavirus, the hamster polyomavirus (HaPV). Two entire HaPV VP1-coding sequences, starting with the authentic and a second upstream ATG, respectively, were subcloned and expressed to high levels in Saccharomyces cerevisiae. The expressed VP1 assembled spontaneously into VLPs with a structure resembling that of the native HaPV capsid. Determination of the subcellular localization revealed a nuclear localization of some particles formed by the N-terminally extended VP1, whereas particles formed by the authentic VP1 were found mainly in the cytoplasmic compartment
Internet: https://hdl.handle.net/20.500.12259/42804
Affiliation(s): Biochemijos katedra
Vytauto Didžiojo universitetas
Appears in Collections:Universiteto mokslo publikacijos / University Research Publications

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