• Mostafa Rezaei-Tavirani, Mona Zamanian-Azodi, Sepideh Rajabi, Ali Masoudi-Nejad, Mohammad Rostami-Nejad, and Sara Rahmatirad.
• Proteomics Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
• Arch Iran Med. 2016 Feb 1; 19 (2): 101-9.

BackgroundAlzheimer and Parkinson diseases (AD and PD) are the two most important neurodegenerative disorders. This paper aims to determine the possible molecular linkage between these two common neurodegenerative diseases by a combination of computational investigations.MethodsAccording to our aim, common sets of identified proteins from the KEGG database were further analyzed based on Gene Ontology (GO) annotation and sequence similarities by the agglomerative hierarchical clustering.  Proteins possessing same characteristics were categorized based on biological features in distinct clusters using the R programming software. In addition to this, by the use of DAVID Program and PPI network analysis, more insight can be achieved.ResultsThe results of this study indicated that 23 proteins are common between these two diseases. Their ontology evaluations by application of clustering methods showed that proteins belonging to a specific cluster indicate discrete properties that are different from other clusters. Furthermore, PPI network analysis confirms that the proteins with similarity ontology and sequence are also in close relationship.ConclusionIn conclusion, assessment of protein features supported the idea that mitochondria are the main malfunction compartment in AD and PD. Some of these common properties are apoptosis and mitochondria oxidation pathways that can be used for drug targeting. Moreover, examination of other neurodegenerative diseases can be helpful for comprehensive understanding of the origin of these diseases.

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