Target Name: SNCB
NCBI ID: G6620
Review Report on SNCB Target / Biomarker Content of Review Report on SNCB Target / Biomarker
SNCB
Other Name(s): Beta-synuclein | SNCB variant 1 | SNCB variant 2 | Synuclein beta, transcript variant 1 | Synuclein beta, transcript variant 2 | SYUB_HUMAN | Synuclein, beta (isoform 2) | synuclein beta | I(2)-synuclein | Beta-synuclein (isoform 1)

SNCB: A Potential Drug Target and Biomarker for Parkinson's Disease

Parkinson's disease is a neurodegenerative disorder characterized by symptoms such as tremors, rigidity, bradykinesia, and postural instability. It affects an estimated 10 million people worldwide and is typically diagnosed in middle-aged and older adults. While the exact cause of Parkinson's disease is not known, it is thought to involve the neurotransmitter dopamine, which is a critical chemical involved in movement and mood regulation.

Recent studies have identified a protein called beta-synuclein (SNCB) as a potential drug target and biomarker for Parkinson's disease. SNCB is a protein that is expressed in the brain and is involved in the formation of beta-synuclein plaques, which are thought to contribute to the neurodegeneration in Parkinson's disease.

Beta-synuclein is a transmembrane protein that is involved in a variety of cellular processes, including the regulation of ion channels, protein synthesis, and intracellular signaling. It is composed of four distinct subunits, which are involved in different aspects of SNCB function. The most well-studied subunit is SNCB1, which is responsible for the formation of beta-synuclein plaques.

In Parkinson's disease, SNCB1 is thought to accumulate in the brain and form beta-synuclein plaques, which are composed of SNCB1 and other protein building blocks. These plaques are thought to disrupt the normal function of nerve cells, leading to the symptoms of Parkinson's disease.

While the exact role of SNCB in the development and progression of Parkinson's disease is not yet fully understood, studies have shown that blocking SNCB activity may be a promising strategy for treating the disease. This is because blocking SNCB activity would reduce the formation of beta-synuclein plaques and potentially slow the progression of neurodegeneration.

One way to block SNCB activity is through the use of small interfering RNA (siRNA). SiRNA is a type of RNA that can be used to reduce the expression of a specific protein by binding to its mRNA. By using siRNA to reduce the expression of SNCB1, researchers have shown that they can reduce the formation of beta-synuclein plaques in Parkinson's disease animal models.

Another approach to blocking SNCB activity is through the use of antibodies. Antibodies are proteins that are produced by the immune system and can be used to target specific proteins in the body. By using antibodies to target SNCB1, researchers have shown that they can reduce the formation of beta-synuclein plaques in Parkinson's disease animal models.

While the use of siRNA and antibodies to block SNCB activity is still in the early stages of research, it is promising as a potential drug target and biomarker for Parkinson's disease. If successful, these treatments may offer a new and effective way to treat this debilitating disorder.

Conclusion

Parkinson's disease is a neurodegenerative disorder that is characterized by symptoms such as tremors, rigidity, bradykinesia, and postural instability. It is thought to involve the neurotransmitter dopamine, which is a critical chemical involved in movement and mood regulation. Recent studies have identified SNCB as a potential drug target and biomarker for Parkinson's disease. By blocking SNCB activity, researchers have shown that these treatments may be an effective way to treat this debilitating disorder. Further research is needed to fully understand the role of SNCB in the development and progression of Parkinson's disease.

Protein Name: Synuclein Beta

Functions: Non-amyloid component of senile plaques found in Alzheimer disease. Could act as a regulator of SNCA aggregation process. Protects neurons from staurosporine and 6-hydroxy dopamine (6OHDA)-stimulated caspase activation in a p53/TP53-dependent manner. Contributes to restore the SNCA anti-apoptotic function abolished by 6OHDA. Not found in the Lewy bodies associated with Parkinson disease

The "SNCB Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about SNCB comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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