In situ interaction determination

a technology of in situ interaction and determination method, which is applied in the field of in situ interaction determination, can solve the problems of inability to identify ligands for such targets, inability to bind to membranes, and inability to bind to membranes, and achieve the effect of rapid identification of ligand:target interactions

Active Publication Date: 2018-08-21
PRESIDENT & FELLOWS OF HARVARD COLLEGE
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patent describes ways to quickly determine how well two different types of molecule called proteins interact with each other. These techniques can be used to study these interactions in both purification and complex matrices containing many small molecular components like certain substances that may have important functions in cells.

Problems solved by technology

This patent describes various techniques used to identify molecules called targets for therapy. These include genetics research, which involves studying how genes are regulated by certain factors like metabolism, growth factor levels, signal transduction pathways, etc., and drug discovery where small molecule drugs are designed to interact specifically with these targets. However, there has always been a problem with selecting pure targets from complex mixtures containing many different types of molecules. Additionally, even if they were found, it could still be challenging to determine whether they work properly due to insolubility issues or other factors involved. Therefore, the technical problem addressed in this patent is finding ways to improve the efficiency and accuracy of identifying specific molecular targets for treatment purposes.

Method used

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Materials and Methods

[0121]Unless otherwise noted, chemical reagents were purchased from Sigma-Aldrich. Water was purified with a Milli-Q purification system. Modified DNA oligonucleotides were synthesized on a PerSeptive Biosystems Expedite 8909 DNA synthesizer. Standard DNA oligonucleotides were purchased from Integrated DNA Technologies. All reagents and phosphoramidites for DNA synthesis were purchased from Glen Research. All oligonucleotides were synthesized and deprotected according to manufacturer's protocols. Oligonucleotides were purified by reverse-phase high-pressure liquid chromatography (HPLC, Agilent 1200) using a C18 stationary phase (Eclipse-XDB C18, 5 μm, 9.4×200 mm) and an acetonitrile / 100 mM triethylammonium acetate gradient. Oligonucleotide concentrations were quantitated by UV spectroscopy using a Nanodrop ND1000 spectrophotometer. Non-commercial oligonucleotides were characterized by LC / ESI-MS; reverse-phase separation was performed on an Alliance 2695 (Waters

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Abstract

Methods, reagents, compositions, and kits for in situ interaction determination (ISID) via interaction-dependent polymerase chain reaction (ID-PCR) are provided herein. ISID technology is useful for rapidly evaluating potential small molecule-target interactions from mixtures in a single solution. ISID is compatible with unpurified targets in biological samples and can be used to evaluate ligand-binding in DNA-encoded chemical libraries in cell lysates. ISID is also useful to screen ligand interactions of proteins or other molecules in their native state, including their native post-translational modifications and any interactions with accessory proteins and metabolites, in ways that better reflect their relevant biological environment. Because ISID is compatible with crude cell lysates, difficult-to-purify, poorly soluble, intrinsically unstable, and aggregation-prone targets may also be compatible with this method, without requiring truncation or other strategies used to promote heterologous expression.

Description

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Claims

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Application Information

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Owner PRESIDENT & FELLOWS OF HARVARD COLLEGE
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