claudins
Enable an agent to identify claudin family members, assess their membrane and barrier states in a specified biological context, and judge which measurements or interventions are supported by evidence.
Bundle → Layer → Finding → Questions Filled
6 bundles · 11 layers · 17 findings · 27 questions
Family member and molecular identity Resolve what counts as a claudin and which biological or experimental form is being considered.
Family membership and naming
Separate family-level identity from member- and species-level assignments.
Member assignment
Record the evidence needed to assign a protein to the claudin family and resolve its name.
- Which curated accession, species and sequence support the proposed claudin member assignment? provenance
- Does the supplied name identify the whole family, one paralogue, an orthologue group or an unresolved historical label? definition
Sequence and preparation
Distinguish endogenous molecular forms from constructs and isolated preparations.
Form-specific identity
Establish which sequence and preparation features constrain interpretation.
- Which isoform, substitutions, tags, truncations or post-translational modifications distinguish this form from the reference sequence? definition
- For an isolated preparation, what evidence establishes identity, purity and the detergent, lipid or membrane environment? measurement
Membrane architecture and junctional assembly Represent claudin topology, interaction surfaces and incorporation into junctional structures.
Topology and accessible regions
Locate regions relevant to extracellular recognition and intracellular interactions.
Structural region assignment
Distinguish experimentally established structure from sequence-based topology predictions.
- Which transmembrane, extracellular and cytoplasmic regions are established for this member, and by what method? provenance
- Which proposed binding epitopes or interaction motifs are accessible in the membrane state under consideration? boundary
Claudin assembly and scaffold coupling
Assess interactions within one membrane, across adjacent cells and with junctional scaffolds.
Assembly compatibility
Require direct evidence for partner compatibility and functional junctional incorporation.
- Which same-membrane and opposing-membrane claudin interactions are demonstrated rather than inferred from coexpression? provenance
- What imaging, interaction or structural evidence establishes junctional assembly and scaffold association for this molecular form? measurement
Paracellular barrier and selectivity Characterise claudin-associated permeability using explicit transported species and experimental conditions.
Ion and solute permeation
Distinguish ion selectivity, molecular passage and broader barrier disruption.
Permeation profile
Frame permeability as a measured profile rather than a binary barrier label.
- Which ions or solutes were tested, and what permeability coefficients, selectivity ratios or fluxes were measured? measurement
- Under which ionic gradients, pH, temperature and epithelial or endothelial conditions does the reported profile hold? boundary
Functional attribution
Assess whether a barrier phenotype can be assigned to a particular claudin.
Member-specific barrier contribution
Separate claudin-dependent effects from changes in cell viability, junction integrity or other transport routes.
- Which matched controls, loss-of-function comparisons or rescue experiments support attribution to this claudin? provenance
- Do resistance, tracer and ion-selectivity measurements distinguish selective permeation from nonspecific leakage or transcellular transport? measurement
Biological context and state transitions Track where claudins occur and how their abundance, localisation and molecular state change.
Tissue expression and localisation
Anchor observations to species, tissue, cell type and cellular compartment.
Context-resolved presence
Keep transcript detection, protein abundance and junctional localisation distinct.
- In which species, tissue, cell type and developmental or experimental state was this claudin detected? boundary
- Does the evidence measure RNA, total protein, surface protein or junctional protein, and at what resolution? measurement
Trafficking, modification and turnover
Capture transitions affecting delivery to, retention at and removal from junctions.
State-change mechanisms
Connect observed claudin transitions to evidenced triggers and downstream readouts.
- Which stimulus or modification is associated with altered claudin trafficking, junctional retention or degradation? provenance
- What time course and reversibility measurements connect the molecular transition to a change in localisation or permeability? measurement
Detection and perturbation evidence Judge the specificity of claudin measurements and the interpretability of interventions.
Member-specific detection
Evaluate whether reagents and assays distinguish the intended claudin and molecular form.
Assay specificity
Require validation appropriate to the member, species, specimen and assay format.
- What knockout, orthogonal assay or cross-reactivity evidence validates detection of the intended claudin? provenance
- Could fixation, permeabilisation, tagging or epitope masking change the apparent abundance or localisation? boundary
Targeted functional perturbation
Assess genetic and binding interventions against specific claudin-dependent outcomes.
Interpretable intervention
Define the intended target state, measurable outcome and controls needed for a supported action.
- Which genetic alteration or binding reagent can test the proposed claudin function in this system, and what establishes target engagement? action
- Which controls distinguish direct claudin effects from compensatory family-member expression, cytotoxicity or general junction disruption? measurement
Evidence and external alignment What the world already says about this thing, gathered so the model can be checked against it.
Reported evidence
Findings from the breadth pass, kept separate from the structural claims.
Check these first
Recalled without web access and unsourced; every item is a lead to verify.
- Which of these check these first hold for the sense of claudins this model covers, and on what evidence? provenance
Kinds and varieties
Recalled without web access and unsourced; every item is a lead to verify.
- Which of these kinds and varieties hold for the sense of claudins this model covers, and on what evidence? provenance
Identifiers and schemes
Recalled without web access and unsourced; every item is a lead to verify.
- Which of these identifiers and schemes hold for the sense of claudins this model covers, and on what evidence? provenance
Real-world use
Recalled without web access and unsourced; every item is a lead to verify.
- Which of these real-world use hold for the sense of claudins this model covers, and on what evidence? provenance
Typical measurements
Recalled without web access and unsourced; every item is a lead to verify.
- Which of these typical measurements hold for the sense of claudins this model covers, and on what evidence? provenance
Failure modes and hazards
Recalled without web access and unsourced; every item is a lead to verify.
- Which of these failure modes and hazards hold for the sense of claudins this model covers, and on what evidence? provenance
Neighbouring kinds and how to tell them apart
Recalled without web access and unsourced; every item is a lead to verify.
- Which of these neighbouring kinds and how to tell them apart hold for the sense of claudins this model covers, and on what evidence? provenance
Classifiers Filled
- Family
- Thing Registry
- Category
- Physical world and living systems
- Entry kind
- thing
- Plane
- PHY
- Domain
- PHY.MAT
- Other names and narrower kinds
- Claudin-2, Claudin-6, Claudin-14, Claudin-9, Claudin-4, Claudin-8, Claudin-7, Claudin-16, Claudin-15, Claudin-11, Claudin-18, Claudin-1
What it is Filled
Claudins are a family of small, four-pass transmembrane proteins that assemble into tight-junction strands and help determine the permeability and ion selectivity of the paracellular pathway between epithelial or endothelial cells.
In scope
- Claudin family membership, species, paralogues and molecular forms
- Membrane topology, extracellular regions and intracellular interaction features
- Cellular localisation, junctional assembly and compatibility between claudin members
- Context-dependent paracellular barrier and selective permeability functions
- Expression, trafficking, turnover and experimentally supported perturbations
- Claudin-specific reagents, preparations and measurement limitations
Out of scope
- Complete tight-junction composition and tissue architecture
- Whole-organ physiology and organism-level homeostasis
- Other junctional protein families such as occludin and junctional adhesion molecules
- Diseases, diagnoses and treatment protocols associated with claudin changes
- Antibodies, drugs, toxins and delivery platforms as independently modelled products
- Gene regulatory networks beyond their directly evidenced effects on claudins
Why it exists Filled
Enable an agent to identify claudin family members, assess their membrane and barrier states in a specified biological context, and judge which measurements or interventions are supported by evidence.
Distinguishing features Filled
- Family assignment requires sequence or curated protein-family evidence; localisation at a tight junction alone does not establish that a protein is a claudin.
- The characteristic four-pass membrane architecture supports recognition, but topology alone does not distinguish claudins from unrelated membrane proteins.
- A claudin name must resolve to a species and family member; different members cannot be treated as interchangeable forms of one substance.
- Detection of claudin RNA or total protein does not establish incorporation into a functional junction.
- A permeability effect must specify the member, transported species and biological context; claudin presence alone does not imply a uniformly tighter barrier.
What robots and AI may and may not do Filled
Must not
- Overstate preliminary research on claudin-targeted therapies as proven treatments.
- Misreport experimental findings or attribute them to the wrong authors.
- Present gene variant findings as a diagnosis for a person.
- Use patient data from studies beyond the consent given.
Only with a human decision
- Endorsing a claudin-targeted therapy for a patient.
May
- Describe claudins and their role in tight junctions from cell biology sources.
- Summarize published research on claudins, citing the studies.
Moral aspects Filled
- Patients with cancers that express claudins may hope for new treatments; honest reporting avoids false hope.
- Research credit matters to scientists.
Who is affected
- Patients
- Researchers
Owners Filled
Steward
Nobody owns the protein family; it belongs to the scientific commons.
Links to other meta-models Filled
parent
- Q1313865 - registry parent class
- Q24784529 - registry parent class
- Q67104298 - registry parent class
What else AI and robots need to interact with it Filled
Identity and identifiers required Filled
- Vercy registry: vr.tr.claudins
- Wikidata: Q420863 (https://www.wikidata.org/wiki/Q420863)
Direct properties required Filled
- Family-member identity: Species, accepted protein name, gene symbol and versioned sequence accession
- Molecular form: Sequence variant, isoform, truncation, fusion tag and modification state
- Membrane topology: Transmembrane-segment assignments, extracellular regions and cytoplasmic termini, with evidence status
- Cellular distribution: Junctional, nonjunctional plasma membrane, intracellular, mixed or unresolved
- Protein abundance: Molecules per cell, amount per sample or explicitly normalised assay units
- Assembly and partner compatibility: Named claudin or scaffold partner, same-membrane or opposing-membrane relationship, and evidence
- Paracellular permeability: Permeability coefficient in cm/s, permeability ratios or tracer flux with explicit units and assay conditions
- Transepithelial electrical resistance: Ω·cm², with blank correction, tissue or culture geometry and measurement conditions
- Perturbation response: Specified genetic, biochemical or binding intervention linked to localisation, abundance or functional outcomes
Recognition not applicable Not applicable
Not applicable
Claudins have no directly visible identifying appearance, and their identification requires molecular evidence rather than visual cues alone.
Capabilities and actions required Filled
- Resolve a claudin label to a species-specific protein member and distinguish endogenous proteins from experimental constructs.
- Assess whether available measurements establish expression, junctional localisation, assembly or permeability function.
- Compare claudin states across matched tissues or experimental systems while retaining assay conditions.
- Select member-specific detection approaches and identify required specificity controls.
- Formulate testable perturbations of claudin expression, localisation or interactions with appropriate functional readouts.
- Identify where evidence supports a member-specific conclusion and where extrapolation across the family remains unresolved.
Hazards and failure modes required Filled
- Inherited claudin defects can cause kidney, hearing or skin disorders.
Standards and interfaces required Filled
- The HUGO Gene Nomenclature Committee provides approved symbols and names for human claudin genes, supporting consistent identification of their encoded proteins.
Context of use required Filled
- Claudins occur at tight junctions in epithelial and endothelial tissues, where their composition helps regulate movement between neighboring cells.
- They are studied in cell biology and biomedical research to investigate tissue barriers, selective ion transport and changes associated with disease.
Sources Filled
- Wikidata item Q420863: claudins - identity and sense of the item
- Wikipedia: Claudin - general description of the item
Open questions
- Does the registry intend claudins across all relevant taxa, and which curated authority should define family membership and naming?
- Which member-specific assembly compatibilities and permeability profiles have sufficient direct evidence to support reusable claims?
- Which reported nonjunctional roles belong within this family model, and which require separate neighbouring models?
- Which assays and reference conditions permit meaningful comparison of claudin function across tissues, culture systems and reconstituted membranes?
- Which detection or perturbation reagents have adequate validation for each member, species and molecular form?
Machine files
Provenance
thing registry research (pass 2) · unreviewed
Built from: models/things/publications/thing-q420863/spec.json