Recombinant Vector for Herpesvirus Transactivator Screening

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Solution Overview

Problem

Current methods fail to effectively disrupt the feedback regulation of herpesvirus transcriptional control elements by herpesvirus transactivators, which is crucial for identifying candidate anti-viral agents and understanding viral replication dynamics.

Innovation Solution

Development of recombinant expression vectors that include a nucleotide sequence encoding a herpesvirus transactivator operably linked to a herpesvirus control element, allowing for the identification of agents that disrupt feedback regulation and providing genetically modified host cells for screening anti-viral agents.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If current methods are used to study herpesvirus transcriptional control, then existing knowledge is maintained, but the ability to identify candidate anti-viral agents is insufficient

Engineering Contradiction:
Improveidentification of candidate anti-viral agentsVSAvoideffectiveness of disrupting feedback regulation
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

The patent introduces a recombinant expression vector as an intermediary system that includes a herpesvirus control element and a reporter gene. This vector serves as a mediator to study the interaction between transactivators and control elements, enabling the identification of agents that disrupt feedback regulation. The vector system translates complex viral regulatory mechanisms into measurable reporter signals that can screen for anti-viral candidates.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The patent replaces direct observation of complex viral transcriptional regulation with a reporter gene system that converts transcriptional activity into measurable signals (such as luminescence or fluorescence). This substitution transforms an invisible biochemical process into a detectable physical signal, enabling high-throughput screening for agents that disrupt feedback regulation.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

2Loss of information

If complex feedback regulation mechanisms are studied directly, then complete viral replication dynamics are observed, but measurement and detection become difficult

Engineering Contradiction:
Improveunderstanding of viral replication dynamicsVSAvoidtranscription levels of transactivator
Core Design Contradiction:
Loss of informationVSDifficulty of detecting and measuring

Solution Approach 1:

The patent creates a simplified copy or model of the viral transcriptional control system using a recombinant expression vector. This vector contains a herpesvirus control element linked to a reporter gene, which replicates the regulatory logic of the viral system in a measurable format. The reporter gene copy allows indirect observation of transactivator activity without directly measuring the complex viral transcriptional machinery.

Inventive Principle:
Principle #26Copying

Solution Approach 2:

The patent employs reporter genes that produce detectable signals (such as luminescence, fluorescence, or color changes) in response to transcriptional activation. These optical signals serve as proxies for measuring transactivator activity and feedback regulation, transforming invisible biochemical events into visible or detectable physical phenomena that can be quantified.

Inventive Principle:
Principle #32Color changes

Data Source

PatentUS10106817B2Compositions and methods of use thereof for identifying anti-viral agents
Publication Date: 2018.10.23 THE J DAVID GLADSTONE INSTITUTES
  • US10106817B2 patent drawing
  • US10106817B2 patent drawing
  • US10106817B2 patent drawing

AI summary

A recombinant expression vector comprising a nucleotide sequence encoding a herpesvirus transactivator, where the nucleotide sequence is operably linked to a herpesvirus control element is provided as are cell lines genetically modified to express a herpesvirus transactivator under the control of a herpesvirus control element. Also provided are methods of identifying agents that disrupt feedback regulation of a herpesvirus transcriptional control element by a herpesvirus transactivator.