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LC3 (Microtubule-Associated Protein 1 Light Chain 3)
LC3 (Microtubule-Associated Protein 1 Light Chain 3)
Introduction
LC3 (Microtubule-Associated Protein 1 Light Chain 3), also known as MAP1LC3 (Microtubule-Associated Protein 1 Light Chain 3), is a fundamental protein in the [autophagy](/entities/autophagy) pathway and serves as a key marker for autophagosome formation. LC3 plays critical roles in neurodegenerative diseases, where autophagy dysfunction is a central pathological feature.
LC3 (Microtubule-Associated Protein 1 Light Chain 3)
Introduction
LC3 (Microtubule-Associated Protein 1 Light Chain 3), also known as MAP1LC3 (Microtubule-Associated Protein 1 Light Chain 3), is a fundamental protein in the [autophagy](/entities/autophagy) pathway and serves as a key marker for autophagosome formation. LC3 plays critical roles in neurodegenerative diseases, where autophagy dysfunction is a central pathological feature.
<table class="infobox infobox-protein">
<tr>
<th class="infobox-header" colspan="2">LC3 (Microtubule-Associated Protein 1 Light Chain 3)</th>
</tr>
<tr>
<td class="label">Protein Name</td>
<td>Microtubule-Associated Protein 1 Light Chain 3</td>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>MAP1LC3 (MAP1A, MAP1B)</td>
</tr>
<tr>
<td class="label">UniProt</td>
<td>[Q9GZF4](https://www.uniprot.org/uniprot/Q9GZF4) (LC3A), [Q9GZY8](https://www.uniprot.org/uniprot/Q9GZY8) (LC3B)</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>~17 kDa</td>
</tr>
<tr>
<td class="label">Aliases</td>
<td>LC3, ATG8, Autophagin</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/ad" style="color:#ef9a9a">AD</a>, <a href="/wiki/ali" style="color:#ef9a9a">ALI</a>, <a href="/wiki/als" style="color:#ef9a9a">ALS</a>, <a href="/wiki/alzheimer" style="color:#ef9a9a">ALZHEIMER</a>, <a href="/wiki/alzheimer's-disease" style="color:#ef9a9a">ALZHEIMER'S DISEASE</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">2307 edges</a></td>
</tr>
</table>
Isoforms
The LC3 family consists of multiple isoforms:
- LC3A (MAP1LC3A) - widely expressed in various tissues
- LC3B (MAP1LC3B) - the most studied isoform, commonly used as an autophagy marker
- LC3C (MAP1LC3C) - more restricted expression pattern
- GABARAP and GATE-16 - related proteins in the ATG8 family[@shpilka2021]
Structure
LC3 belongs to the ATG8 family of proteins and undergoes post-translational modifications essential for its function. The protein contains:
- An N-terminal helical domain
- A ubiquitin-like (Ubl) domain that undergoes lipidation
- A C-terminal glycine exposed by ATG4 protease cleavage[@ichimura2020]
The lipidation process converts LC3-I to LC3-II (phosphatidylethanolamine-conjugated form), which is the active form that localizes to autophagosomal membranes.
Role in Autophagy
LC3 is central to the autophagy process:
Role in Neurodegenerative Diseases
Alzheimer Disease
In Alzheimer disease (AD), autophagy is significantly impaired at multiple stages:
- Reduced autophagosome-lysosome fusion leads to accumulation of autophagic vacuoles in [neurons](/entities/neurons)[@nixon2019a]
- LC3-positive autophagosomes accumulate in vulnerable neurons, indicating attempted but failed autophagy
- [Amyloid-beta](/proteins/amyloid-beta) (A beta) plaques can be enclosed by LC3-positive membranes, suggesting autophagy attempts to clear A beta aggregates
- The [presenilin](/proteins/presenilin-1-protein) mutations in familial AD impair lysosomal function, downstream of LC3-mediated autophagy[@lee2020]
Parkinson Disease
In Parkinson disease (PD), LC3 and autophagy play critical roles:
- [Alpha-synuclein](/proteins/alpha-synuclein) is degraded by both autophagy and the proteasome
- LC3-positive inclusions are found in PD brains, particularly in [Lewy bodies](/diseases/lewy-body-disease)
- Mutations in [GBA](/genes/gba) (glucocerebrosidase) impair autophagy flux and lead to alpha-synuclein accumulation
- PINK1 and Parkin-mediated mitophagy involves LC3 recruitment to damaged mitochondria[@pickrell2019]
Amyotrophic Lateral Sclerosis
In ALS, autophagy dysfunction contributes to disease progression:
- Mutations in [C9orf72](/genes/c9orf72) dipeptide repeat proteins impair autophagy
- [TDP-43](/mechanisms/tdp-43-proteinopathy) pathology disrupts autophagy-lysosomal pathways
- LC3 aggregation is observed in motor neurons of ALS patients[@chen2020]
Therapeutic Implications
Targeting the autophagy pathway via LC3 modulation represents a therapeutic strategy:
- Autophagy enhancers (rapamycin, carbamazepine) promote LC3-mediated autophagosome formation
- Gene therapy approaches to increase LC3 expression are under investigation
- Small molecules that facilitate LC3 lipidation are being developed[@rubinsztein2019]
Interactions
LC3 interacts with numerous proteins:
- [p62/SQSTM1](/proteins/p62-protein) - autophagy receptor for selective autophagy
- [PINK1](/genes/pink1) - kinase activated in damaged mitochondria
- [Parkin](/genes/parkin) - E3 ubiquitin ligase in mitophagy
- [ATG proteins](/proteins/atg5-protein) - autophagy machinery components
- [OPTN](/genes/optn) - optineurin, autophagy receptor
- [NBR1](/genes/nbr1) - autophagy receptor[@johansen2021]
Pathway & Interaction Diagram
Interactive diagram showing LC3's key relationships in the SciDEX knowledge graph (15 connections shown).
See Also
- [Autophagy](/mechanisms/autophagy)
- [Mitophagy](/mechanisms/mitophagy)
- [p62 Protein](/proteins/p62-protein)
- [Alpha-synuclein](/proteins/alpha-synuclein)
- [Alzheimer Disease](/diseases/alzheimers-disease)
- [Parkinson Disease](/diseases/parkinsons-disease)
References
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | proteins-lc3-protein |
| kg_node_id | LC3PROTEIN |
| entity_type | protein |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-d8d9ef884ac0 |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'proteins-lc3-protein'} |
| _schema_version | 1 |
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