Light-Sensitive Synthetic Regulator for Protein Function Control

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Solution Overview

Problem

There is a need for methods to precisely regulate protein function, particularly in responding to external signals, as existing technologies lack effective mechanisms for controlling protein activity across different domains and environments.

Innovation Solution

A light-sensitive synthetic regulator is developed, comprising a linker domain, a photoisomerizable group, and a ligand that binds to a protein's allosteric site, allowing for modulation of protein function through light exposure, enabling changes in protein activity and conformation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If a light-sensitive synthetic regulator is used to control protein function, then precise regulation of protein activity is achieved, but device complexity increases

Engineering Contradiction:
Improveprecise regulation of protein activityVSAvoidstructure of synthetic regulator
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The synthetic regulator is divided into distinct functional domains: a ligand-binding domain that recognizes and binds to the target protein, a photoisomerizable group that undergoes light-induced conformational changes, and a linker domain that connects these elements. This segmentation allows each component to perform its specific function independently while contributing to the overall precise control of protein activity.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The synthetic regulator combines multiple chemical moieties with different properties into a single hybrid molecule. The ligand-binding domain provides high affinity and specificity for the target protein, the photoisomerizable group provides light sensitivity and conformational switching capability, and the linker provides structural flexibility. This composite structure enables precise protein regulation through light exposure.

Inventive Principle:
Principle #40Composite materials

2Adaptability or versatility

If allosteric control mechanism is used to regulate protein function, then long-distance conformational control is achieved, but difficulty of detecting and measuring increases

Engineering Contradiction:
Improvelong-distance conformational controlVSAvoidconformational changes
Core Design Contradiction:
Adaptability or versatilityVSDifficulty of detecting and measuring

Solution Approach 1:

The photoisomerizable group undergoes light-induced isomerization that can be detected through changes in optical properties such as absorption spectra or fluorescence. This provides a measurable signal that reports on the conformational state of the synthetic regulator and its effect on the target protein, making the allosteric control mechanism detectable.

Inventive Principle:
Principle #32Color changes

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The light-regulated protein system allows for precise control of protein activity, altering binding affinities and functional states in response to light, enabling applications in cellular regulation and signaling.

Implementation Method 1

a photoisomerizable group, which undergoes photoisomerization to induce a conformational change in the regulator

Methodology Applied
Scientific EffectPhotoisomerization: Photochromism

Data Source

PatentUS9629911B2Photoreactive regulator of protein function and methods of use thereof
Publication Date: 2017.04.25 RGT UNIV OF CALIFORNIA
  • US9629911B2 patent drawing
  • US9629911B2 patent drawing
  • US9629911B2 patent drawing

AI summary

The present invention provides a synthetic regulator of protein function, which regulator is a light-sensitive regulator. The present invention further provides a light-regulated polypeptide that includes a subject synthetic regulator. Also provided are cells and membranes comprising a subject light-regulated polypeptide. The present invention further provides methods of modulating protein function, involving use of light. The present invention further provides methods of identifying agents that modulate protein function.