Target intelligence / Profile preview

Large ribosomal subunit protein bL35m (mitochondrial) (MRPL35)

Target
MRPL35
Molecular classification
Ribosomal protein, Mitochondrial ribosomal protein (component of mitochondrial large [39S] ribosomal subunit), Structural constituent of ribosome, Other (not a classic receptor, enzyme, transporter, ion channel, or transcription factor; rather, a structural protein essential for mitochondrial translation)
01

Overview

Large ribosomal subunit protein bL35m (MRPL35) is a nuclear-encoded protein that is incorporated into the large 39S subunit of the mitochondrial ribosome (mitoribosome)[3][5][7]. It is essential for mitochondrial protein synthesis and thus for proper mitochondrial function and cellular energy metabolism[5][2]. MRPL35 is robustly expressed in tissues and is highly conserved across species[3][2]. Dysfunction or altered expression of MRPL35 has been associated with changes in cell proliferation, invasion, and glutamine metabolism, particularly in the context of non-small cell lung cancer, where it promotes tumor growth by upregulating SLC7A5 expression[1]. Its core role is structural—helping assemble the mitoribosome for translation of mitochondrial mRNAs. While MRPL35 is not a classic druggable target (e.g., receptor or enzyme), recent research points to its potential as a therapeutic target due to its emergent roles in cancer metabolism[1]. There are currently no approved drugs targeting MRPL35, likely reflecting the essential nature of the mitochondrial translation machinery and the safety risks of systemic inhibition[2][5].

Other names
MRPL35Large ribosomal subunit protein bL35mL35mtMRP-L35bL35m39S ribosomal protein L35, mitochondrialBM-007Mitochondrial large ribosomal subunit protein bL35m
02

Biological functions

Protein synthesis within mitochondrion (mitochondrial translation)Cellular assembly and function of the mitoribosome complexSupports cell proliferation and invasion (in cancer context)Regulates glutamine metabolism in tumor cells
03

Disease associations

Cancer (particularly implicated in non-small cell lung cancer)Mitochondrial diseases (by analogy to other mitochondrial ribosomal proteins)Developmental disorders (suggested by relation to early embryonic lethality when knocked out, though direct disease association data for MRPL35 may be limited)
04

Safety considerations

Potential challenge is essential cellular function: targeting MRPL35 may impair mitochondrial translation and ATP production in healthy tissues, leading to toxicityPossible risk of early embryonic lethality, severe mitochondrial dysfunction

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