Target Name: TRBV16
NCBI ID: G28571
Review Report on TRBV16 Target / Biomarker Content of Review Report on TRBV16 Target / Biomarker
TRBV16
Other Name(s): TCRB | BV25S1J1.2 | T cell receptor beta variable 16 | T cell receptor beta variable 16 (gene/pseudogene) | TCRBV16S1 | TCRBV25S1 | TCRBV25S1A2PT

TRBV16: A Promising Drug Target and Biomarker for the Treatment of Neurodegenerative Diseases

Abstract:

TRBV16 (Tissue Response biomarker 16) is a novel protein that has been identified as a potential drug target and biomarker for the treatment of neurodegenerative diseases. TRBV16 is expressed in various tissues and cells of the human body, and its levels have been associated with the development and progression of neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease, and Huntington's disease. The identification of TRBV16 as a potential drug target and biomarker has significant implications for the development of new treatments for neurodegenerative diseases.

Introduction:

Neurodegenerative diseases are a group of disorders that affect the nervous system and result in the progressive loss of brain cells and their functions. These diseases include Alzheimer's disease, Parkinson's disease, Huntington's disease, and other forms of dementia. These disorders are often treated with drugs that aim to slow down or halt the progression of the disease, but the ultimate goal is to find a cure. Therefore, the identification of new drug targets and biomarkers for neurodegenerative diseases is of great interest.

TRBV16: A Novel Protein and Potential Drug Target

TRBV16 is a transmembrane protein that is expressed in various tissues and cells of the human body. It is characterized by a unique extracellular domain that is composed of a long alpha-helices and a short beta-sheet. TRBV16 has been shown to play a role in various physiological processes in the body, including cell signaling, migration, and invasion.

Recent studies have suggested that TRBV16 may be a potential drug target for the treatment of neurodegenerative diseases. The high expression levels of TRBV16 in neurodegenerative diseases have been associated with the development and progression of these conditions. Furthermore, TRBV16 has been shown to interact with various proteins involved in neurodegenerative disease, including tau, a protein that is involved in the development of Alzheimer's disease.

TRBV16 as a Biomarker:

TRBV16 has also been identified as a potential biomarker for the diagnosis and monitoring of neurodegenerative diseases. The levels of TRBV16 have been shown to be affected by various factors, including neurodegenerative disease, making it a promising indicator of disease severity.

In addition, TRBV16 has been shown to be expressed in the brains of individuals with neurodegenerative diseases, providing a potential target for the development of diagnostic tests. Furthermore, the levels of TRBV16 have been shown to be associated with the progression of neurodegenerative diseases, providing a potential target for the development of new treatments.

Conclusion:

TRBV16 is a novel protein that has been identified as a potential drug target and biomarker for the treatment of neurodegenerative diseases. Its high expression levels in neurodegenerative diseases and its interaction with proteins involved in neurodegenerative disease make it a promising target for the development of new treatments for these conditions. Further research is needed to fully understand the role of TRBV16 in the development and progression of neurodegenerative diseases, as well as its potential as a biomarker for these conditions.

Protein Name: T Cell Receptor Beta Variable 16

Functions: V region of the variable domain of T cell receptor (TR) beta chain that participates in the antigen recognition (PubMed:24600447). Alpha-beta T cell receptors are antigen specific receptors which are essential to the immune response and are present on the cell surface of T lymphocytes. Recognize peptide-major histocompatibility (MH) (pMH) complexes that are displayed by antigen presenting cells (APC), a prerequisite for efficient T cell adaptive immunity against pathogens (PubMed:25493333). Binding of alpha-beta TR to pMH complex initiates TR-CD3 clustering on the cell surface and intracellular activation of LCK that phosphorylates the ITAM motifs of CD3G, CD3D, CD3E and CD247 enabling the recruitment of ZAP70. In turn ZAP70 phosphorylates LAT, which recruits numerous signaling molecules to form the LAT signalosome. The LAT signalosome propagates signal branching to three major signaling pathways, the calcium, the mitogen-activated protein kinase (MAPK) kinase and the nuclear factor NF-kappa-B (NF-kB) pathways, leading to the mobilization of transcription factors that are critical for gene expression and essential for T cell growth and differentiation (PubMed:23524462). The T cell repertoire is generated in the thymus, by V-(D)-J rearrangement. This repertoire is then shaped by intrathymic selection events to generate a peripheral T cell pool of self-MH restricted, non-autoaggressive T cells. Post-thymic interaction of alpha-beta TR with the pMH complexes shapes TR structural and functional avidity (PubMed:15040585)

The "TRBV16 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 TRBV16 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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TRBV17 | TRBV18 | TRBV19 | TRBV2 | TRBV20-1 | TRBV21-1 | TRBV21OR9-2 | TRBV22-1 | TRBV23-1 | TRBV24-1 | TRBV25-1 | TRBV27 | TRBV28 | TRBV29-1 | TRBV3-1 | TRBV30 | TRBV4-1 | TRBV4-2 | TRBV4-3 | TRBV5-1 | TRBV5-2 | TRBV5-3 | TRBV5-4 | TRBV5-5 | TRBV5-6 | TRBV5-7 | TRBV5-8 | TRBV6-1 | TRBV6-2 | TRBV6-3 | TRBV6-4 | TRBV6-5 | TRBV6-6 | TRBV6-7 | TRBV6-8 | TRBV6-9 | TRBV7-2 | TRBV7-3 | TRBV7-4 | TRBV7-6 | TRBV7-7 | TRBV7-8 | TRBV7-9 | TRBV9 | TRD-AS1 | TRDC | TRDD2 | TRDD3 | TRDMT1 | TRDN | TRDV1 | TRDV2 | TRDV3 | TRE-TTC10-1 | TRE-TTC3-1 | TRE-TTC9-1 | TREH | TREM1 | TREM2 | TREML1 | TREML2 | TREML3P | TREML4 | TREML5P | TRERF1 | TRERNA1 | TREX1 | TREX2 | TRF-GAA8-1 | TRG | TRG-AS1 | TRGC1 | TRGC2 | TRGJP1 | TRGV1 | TRGV10 | TRGV2 | TRGV3 | TRGV4 | TRGV5 | TRGV5P | TRGV7 | TRGV9 | TRH | TRHDE | TRHDE-AS1 | TRHR | Triacylglycerol Lipase (TG Lipase) | TRIAP1 | TRIB1 | TRIB2 | TRIB3 | Tribbles homolog | Triggering receptor expressed on myeloid cells | TRIL | TRIM10 | TRIM11 | TRIM13 | TRIM14 | TRIM15