Sentence examples for engineered envelope from inspiring English sources

Recent improvements have come from combining lentiviral vectors with engineered envelope proteins, which now allow targeting of cell entry to any cell population of interest, as well as the transduction of quiescent cells of the haematopoietic system.

Both naturally occurring and engineered chromatin-envelope interactions are sufficient to allow chromatin compaction forces to drive distortions of the nuclear envelope.

The creation of lentiviral vectors with highly engineered EboZ envelopes improved the performance of the system and should also increase its safety since only minimal regions of the EboZ envelope, which lack the toxic domain, are used.

An RGD-containing peptide, comprising 23 amino acids from the foot-and-mouth disease virus (FMDV) VP1 protein was engineered into the envelope of Autographa californica nuclear polyhedrosis virus surface (AcNPV) using two different display strategies.

Novel approaches for cell targeting with engineered lentiviral vector envelope pseudotypes are exciting new developments in this field (Anliker et al, 2010; Frecha et al, 2012; Zhou & Buchholz, 2013).

To evaluate the role of SL-1 in the context of its native environment, the Mtb cell envelope, we engineered a strain of Mtb in which SL-1 biosynthesis is abolished at its first committed step, sulfation of trehalose by the sulfotransferase Stf0 (see entire pathway elaborated in Supplementary Figure 1).

Also unbeknownst to most people is that all aspects of the envelopes are engineered like a German car -- from making sure the enclosed cards can be extracted from the envelopes easily to making sure the light hits the paper correctly.

In this work, two multiple baculovirus expression vectors (BEVs) with PRRS virus envelope proteins were engineered in order to generate PRRS VLPs: on the one hand, Gp5 and M cDNAs were cloned to generate the pBAC-Gp5M vector; on the other hand, Gp2, Gp3, Gp4 and E cDNAs have been cloned to generate the pBAC-Gp234E vector.

The corresponding viral envelope proteins are engineered to display a FLAG epitope, which is a polypeptide protein tag, and to also display a polyhistidine tag at their N and C termini for specific and sensitive immunological identification, as well as for gentle and easy purification.

Stability of the cloned genome is ensured by the incorporation of a stabilizing intron sequence engineered at the junction of envelope (E) and the non-structural 1 (NS1) gene.

Corn calli were genetically engineered to produce PRRSV viral envelope-associated M protein.