Active Cells, Biochemistry & Physiology Genetics & Molecular Biology

The Birth of the Autophagosome

In plain English

AI plain-English summary

Every living cell runs a continuous recycling programme called autophagy, which breaks down damaged parts and invading microbes to keep itself healthy. When this process falters, cells age faster and become vulnerable to disease. Scientists know the broad outline of how autophagy starts, but the precise molecular choreography remains unclear—especially for selective autophagy, which targets specific cargo for disposal. This project homes in on a protein called Rab1, which preliminary data suggest acts as a crucial connector between the cell’s recycling machinery and the items marked for destruction. The researcher will map exactly how Rab1 forms signalling complexes and test its role in two forms of selective autophagy: mitophagy, which clears worn-out mitochondria, and aggrephagy, which removes toxic protein clumps. This is fundamental cell biology with no immediate clinical application. However, impaired autophagy is now recognised as a hallmark of ageing, and understanding Rab1’s role could eventually open avenues for interventions that maintain cellular health—much as earlier fundamental work on autophagy revealed its links to neurodegeneration, infection, and cancer.

View original technical description
Autophagy, the cell's recycling program, plays a critical role in maintaining cellular health through recycling nutrients and by removing threats to cellular survival, be it damaged organelles or invading pathogens. Significantly, impaired autophagy is now recognized as a hallmark of ageing, highlighting its importance alongside factors like loss of proteostasis or epigenetic alterations. The mechanism of autophagy initiation is understood in broad lines but the exact sequence of events, and how the autophagy machinery is integrated is not well understood. This is especially true for pathways of selective autophagy which target and eliminate specific cargo. My preliminary data has now uncovered a putative crucial new aspect of selective autophagy regulation through the GTPase Rab1 and its interaction with the autophagy machinery. Rab1 is critical for autophagy but has been largely overlooked. I propose that Rab1 is a cornerstone helping connect key autophagy machinery to autophagic cargo.I aim to first characterize the molecular mechanisms of Rab1-mediated signalling complexes. I will then characterize the mechanism and role of Rab1 in different forms of selective autophagy in cells, including mitophagy and aggrephagy. This proposal will advance the mechanistic insight of how autophagy is initiated and regulated with important implications for human health.

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Researchers

Alexander van Vliet (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

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Tumour Cell Death
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Original classification

Career Development Award

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