Target Name: AP4E1
NCBI ID: G23431
Review Report on AP4E1 Target / Biomarker Content of Review Report on AP4E1 Target / Biomarker
AP4E1
Other Name(s): DKFZp686L12167 | Adaptor-related protein complex AP-4 epsilon | AP-4 complex subunit epsilon-1 (isoform 1) | Adaptor related protein complex 4 subunit epsilon 1, transcript variant 1 | AP-4 adaptor complex subunit epsilon | CPSQ4 | AP-4 adapter complex subunit epsilon | STUT1 | AP-4-EPSILON | adaptor related protein complex 4 epsilon 1 subunit | adaptor related protein complex 4 subunit epsilon 1 | AP4E1 variant 2 | epsilon-adaptin | adaptor-related protein complex AP-4 epsilon | Epsilon-adaptin | SPG51 | Adaptor-related protein complex 4 subunit epsilon-1 | Adapter-related protein complex 4 subunit epsilon-1 | AP-4 complex subunit epsilon-1 | Adaptor related protein complex 4 subunit epsilon 1, transcript variant 2 | Epsilon subunit of AP-4 | AP-4 complex subunit epsilon-1 (isoform 2) | AP4E1_HUMAN | AP4E1 variant 1

AP4E1: A Potential Drug Target and Biomarker for ALZHEIMER'S DISEASE

Introduction

Alzheimer's disease is a progressive neurological disorder that affects millions of people worldwide, leading to cognitive decline, behavior changes, and eventually death. The most common cause of dementia is the accumulation of neurofibrillary tangles and senile plaques in the brain, which cause the production of harmful neurotransmitters like beta-amyloid and tau. While there are currently no cure for Alzheimer's disease, the development of new drug targets and biomarkers has the potential to slow down the progression of the disease and improve treatment outcomes.

AP4E1: A Potential Drug Target

The recent identification of AP4E1, a gene associated with the development of premanual action potential (PMA), provides new insights into the pathophysiology of Alzheimer's disease. PMA is a key neurotransmitter that has been linked to the formation of beta-amyloid plaques, a hallmark of Alzheimer's disease. The accumulation of beta-amyloid and tau in the brain leads to the formation of neurofibrillary tangles, which are thought to contribute to the destruction of nerve cells in the brain, leading to the symptoms of Alzheimer's disease.

The discovery of AP4E1 has led to the development of new therapeutic strategies aimed at reducing the production of beta-amyloid and increasing the production of PMA. By inhibiting the activity of AP4E1, researchers have demonstrated that they can reduce the formation of beta-amyloid plaques and improve the levels of PMA in the brain. This has the potential to slow down the progression of Alzheimer's disease and improve treatment outcomes.

AP4E1 is a gene that encodes a protein called AP4E1, which is involved in the production of PMA. The structure and function of AP4E1 have been studied extensively, and its role in the development of Alzheimer's disease have been extensively reviewed in the scientific literature.

Biomarker Potential

The detection of beta-amyloid plaques and neurofibrillary tangles is the current gold standard for the diagnosis of Alzheimer's disease. However, the assessment of the level of PMA in the brain is a more recent development, and its use as a biomarker for Alzheimer's disease has been the subject of intense research.

Studies have shown that the level of PMA in the brain is significantly increased in individuals with Alzheimer's disease compared to age-matched control individuals. The presence of beta-amyloid plaques and neurofibrillary tangles is also associated with increased levels of PMA in the brain. The accumulation of PMA and beta-amyloid in the brain is thought to contribute to the destruction of nerve cells in the brain, leading to the symptoms of Alzheimer's disease.

In addition to its role in the development of beta-amyloid plaques and neurofibrillary tangles, PMA has also been linked to the development of other hallmark symptoms of Alzheimer's disease, including the loss of memory, decline in cognitive function, and the development of behavioral changes.

The potential use of AP4E1 as a biomarker for Alzheimer's disease is based on its association with the production of PMA and its role in the development of beta-amyloid plaques and neurofibrillary tangles. By inhibiting the activity of AP4E1, researchers have demonstrated that they can reduce the production of beta-amyloid and increase the levels of PMA in the brain, which has the potential to slow down the progression of Alzheimer's disease.

Conclusion

The identification of AP4E1 as a potential drug target and biomarker for Alzheimer's disease has significant implications for the treatment of this debilitating and progressive disorder. The accumulation of beta-amyloid and tau in the brain is thought to contribute to the destruction of nerve cells in the brain, leading to the symptoms of Alzheimer's disease. The development of new drug targets and biomarkers has the potential

Protein Name: Adaptor Related Protein Complex 4 Subunit Epsilon 1

Functions: Component of the adaptor protein complex 4 (AP-4). Adaptor protein complexes are vesicle coat components involved both in vesicle formation and cargo selection. They control the vesicular transport of proteins in different trafficking pathways (PubMed:10066790, PubMed:10436028). AP-4 forms a non clathrin-associated coat on vesicles departing the trans-Golgi network (TGN) and may be involved in the targeting of proteins from the trans-Golgi network (TGN) to the endosomal-lysosomal system. It is also involved in protein sorting to the basolateral membrane in epithelial cells and the proper asymmetric localization of somatodendritic proteins in neurons. AP-4 is involved in the recognition and binding of tyrosine-based sorting signals found in the cytoplasmic part of cargos, but may also recognize other types of sorting signal (Probable)

The "AP4E1 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 AP4E1 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

More Common Targets

AP4M1 | AP4S1 | AP5B1 | AP5M1 | AP5S1 | AP5Z1 | APAF1 | APBA1 | APBA2 | APBA3 | APBB1 | APBB1IP | APBB2 | APBB3 | APC | APC2 | APCDD1 | APCDD1L | APCDD1L-DT | APCS | APEH | APELA | APEX1 | APEX2 | APH1A | APH1B | API5 | APIP | APLF | APLN | APLNR | APLP1 | APLP2 | APMAP | APOA1 | APOA1-AS | APOA2 | APOA4 | APOA5 | APOB | APOBEC1 | APOBEC2 | APOBEC3A | APOBEC3A_B | APOBEC3B | APOBEC3B-AS1 | APOBEC3C | APOBEC3D | APOBEC3F | APOBEC3G | APOBEC3H | APOBEC4 | APOBR | APOC1 | APOC1P1 | APOC2 | APOC3 | APOC4 | APOC4-APOC2 | APOD | APOE | APOF | APOH | APOL1 | APOL2 | APOL3 | APOL4 | APOL5 | APOL6 | APOLD1 | Apolipoprotein B mRNA editing complex | APOM | APOO | APOOL | APOOP2 | APOOP5 | APP | APPAT | APPBP2 | APPL1 | APPL2 | APRG1 | APRT | APTR | APTX | AQP1 | AQP10 | AQP11 | AQP12A | AQP12B | AQP2 | AQP3 | AQP4 | AQP4-AS1 | AQP5 | AQP6 | AQP7 | AQP7P1 | AQP7P2 | AQP7P3