A Cell-Based Seeding Assay for Huntingtin Aggregation
- 技術優勢
- SpecificSensitiveHigh throughputCorrelates with disease progressionCompatible with biological samples
- 技術應用
- Huntington's Disease diagnosis Drug discoveryClinical trial biomarker
- 詳細技術說明
- A novel high throughput cell-based seeding assay was developed to detect mutant HTT proteins. This approach utilizes a transgenic cell line that expresses a form of mHTT, which is linked to a green fluorescent protein (GFP), making any aggregates easily quantifiable. The cell line has a very low baseline level of aggregates. However, it can be highly specifically induced to form aggregates with even very small aggregate seeds are introduced from HD patients or mouse samples. The readout correlates well with the amount of seeds added and with the disease stage of the HD patients.
- *Abstract
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UCLA researchers from the Department of Psychiatry has created a novel cell-based seeding assay for sensitive, specific and high throughput detection of mutant Huntingtin proteins in biological samples.
- *Principal Investigation
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Name: Chung-Ying Lee
Department:
Name: Nan Wang
Department:
Name: Xiangdong Yang
Department:
- 其他
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Background
Huntington’s disease (HD) is a lethal genetic disorder that is caused by mutatations in thehuntingtin protein (mHTT). Genetic errors cause an elongated repeat motif to result in a polyglutamine (polyQ) stretch in the expressed protein, causing it to form aggregates. These aggregates accumulate in the nerve cells eventually lead to their breakdown, incurring debilitating effects. Current molecular methods of diagnosing HD include direct detection, in vitro aggregation detection and cell based detection. Direct detection of HTT uses antibodies, which can only detect a subset of HTT in soluble, monomer forms. In vitro aggregation detection lacks sensitivity. Other existing cell based detection approaches are prone to false positives and are labor intensive.
Additional Technologies by these Inventors
- Novel Mouse Model for Huntingtons Disease
- Transgenic Mouse Model of Parkinson's Disease with Age-Dependent Hypokinetic Motor Deficits, Dopaminergic Neuron Loss, and Alpha Synuclein Accumulation
- Rosa HD
Tech ID/UC Case
29135/2018-193-0
Related Cases
2018-193-0
- 國家/地區
- 美國
