Anti-MRPS35 antibody [EPR11731(2)] - BSA and Azide free

Supplementary info

This supplementary information is collated from multiple sources and compiled automatically.

Activity summary

MRPS35 also known as 28S ribosomal protein S35 or mitochondrial ribosomal protein S35 is a component of the small subunit of the mitochondrial ribosome. This protein is integral to mitochondrial protein synthesis and weighs approximately 39 kDa. It is expressed widely in human tissues but shows higher expression in tissues with high energy demand like skeletal muscle and heart. MRPS35 plays a mechanical role in facilitating the translation of mitochondrial mRNA to proteins necessary for mitochondrial function.

Biological function summary

MRPS35 is essential in mitochondrial ribosome assembly and protein synthesis. As part of the mitochondrial ribosomal small subunit it contributes to the assembly of ribosomes and the translation of essential proteins for mitochondrial energy production. This protein partners with other mitochondrial ribosomal proteins and plays a role in the synthesis of oxidative phosphorylation components an important metabolic pathway for ATP production.

Pathways

MRPS35 is significant in cellular respiratory processes. It plays a role in the oxidative phosphorylation pathway which is important for ATP production. MRPS35 interacts with other mitochondrial ribosomal proteins like MRPS30 to ensure efficient assembly and function of the mitochondrial ribosome. The proper synthesis of mitochondrial proteins is critical for maintaining the electron transport chain's function.

Associated diseases and disorders

MRPS35 relates to certain mitochondrial disorders and possibly metabolic syndromes. Defects in mitochondrial protein synthesis can lead to conditions such as mitochondrial myopathy and MELAS syndrome (Mitochondrial Encephalopathy Lactic Acidosis and Stroke-like episodes). MRPS35 through its role in mitochondrial protein synthesis also has connections with proteins like MRPL44 which is another component of the mitochondrial ribosome where defects in these proteins can potentially exacerbate mitochondrial dysfunction.