Asgpr-binding compounds for the degradation of extracellular proteins
US-2024424108-A1 · Dec 26, 2024 · US
US10889609B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10889609-B2 |
| Application number | US-201515758782-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 14, 2015 |
| Priority date | Sep 9, 2015 |
| Publication date | Jan 12, 2021 |
| Grant date | Jan 12, 2021 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention relates to a mannitol-based amphipathic compound, a method of preparing the same, a method of extracting, solubilizing, stabilizing or crystallizing a membrane protein using the compound, and a method of analyzing a structure of the membrane protein under an electron microscope using the compound. When the mannitol-based compound according to the present invention is used, the membrane protein can be stably stored in an aqueous solution for a prolonged period of time and thus can be applied to analysis of functions and structures thereof. Since the analysis of the structures and functions of the membrane protein is one of the fields of most interest in biology and chemistry currently, and more than half of new drugs currently in development are targeting membrane proteins, the present invention is applicable to research on the structures of membrane proteins closely related to the development of the new drugs.
Opening claim text (preview).
The invention claimed is: 1. A composition for extracting, solubilizing, stabilizing or crystallizing a membrane protein, or analyzing a structure of the membrane protein using an electron microscope, the composition comprising a compound represented by the following Formula 1: wherein R 1 and R 2 are each independently an unsubstituted C 5 -C 20 alkyl group, a substituted or unsubstituted C 5 -C 20 cycloalkyl group, or a substituted or unsubstituted C 5 -C 20 aryl group; and X 1 , X 2 , X 3 , and X 4 are each independently a glucose or maltose, whereby the composition is for extracting, solubilizing, stabilizing or crystallizing a membrane protein, or analyzing the structure of the membrane protein using the electron microscope. 2. The composition of claim 1 , wherein each of R 1 and R 2 is C 7 -C 18 alkyl group; R 1 and R 2 are the same. 3. The composition of claim 1 , wherein the compound is represented by the following Formula 2, Formula 3, Formula 4, Formula 5, Formula 6, Formula 7, Formula 8, Formula 9, Formula 10, or Formula 11: 4. The composition of claim 1 , wherein the compound is an amphipathic molecule for extracting, solubilizing, stabilizing or crystallizing a membrane protein. 5. The composition of claim 1 , wherein the compound has a critical micellar concentration (CMC) of 1×10 −4 mM to 1.0 mM in an aqueous solution. 6. The composition of claim 1 , wherein the compound is an amphipathic molecule capable of forming a complex with the membrane protein for analyzing a structure of the membrane protein using an electron microscope. 7. The composition of claim 1 , wherein the composition is a micelle, a liposome, an emulsion, or a nanoparticle formulation.
from acetals, e.g. by dealcoholysis · CPC title
as complexes · CPC title
Extraction; Separation; Purification · CPC title
Intracellular protein regulatory factors and their receptors, e.g. including ion channels · CPC title
Processes for the preparation of sugar derivatives · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.