Kategóriák: Minden - receptors - activation - phosphorylation

a Bradley Campbell 1 éve

89

Classical receptors

Receptors are specialized protein molecules critical for cellular signaling and can be broadly categorized into classical receptors, G-protein coupled receptors (GPCRs), ligand-gated ion channels, kinase-linked receptors, and nuclear receptors.

Classical receptors

I apologize, i had this done last week and just neglected to press submit, I will be on top of it for the rest of the quarter

Classical receptors

Nuclear receptors

Types of nuclear receptors
Type 2

common receptor types

xenobiotic receptors

Activates drug metabolizing enzymes such as CYTP3A

Cholesterol receptors

Fatty acid receptors

form homodimers with Retinoid x receptor

primarily in nucleus

Hybrid

Examples

Vitamin D receptor

Thyroid hormone receptor

Form obligate heterodimers with RXR

Tyoe 1

primarily bind:

oestrogen, progesterone, androgen

Mineralocorticoids

Glucocorticoids

Form homodimers on ligand

Found in cytoplasm

Some of the slowest response times
Hours to days
Orphan receptors
Subtopic
Example

RXR receptor

No well defined ligand
Ligand examples
Vitamin D
many hormones
N terminal domain

Controls interactions with cofactors

C terminal domain

Governs nuclear localization

Ligand binding domain
DNA Recognition and binding domain

Major drug targets

Drug target exceptions
Drugs target nucleic acids

Antisense and siRNA targets

DNA/RNA metabolism

Drugs target other specific protiens

Signaling protiens

structural protiens

Transporters
Enzymes
ion channels
Main topic of lecture

Kinase linked receptors

Receptor examples
Cytokine receptors

Associate with Cytosolic tyrosine kinases

Serine/Threonine kinase

Transforming growth factor receptor

Receptor tyrosine kinases

Toll like receptors

Growth factor receptors

Ligand examples:
bacterial lipopolysaccharides
Cytokines
Growth factors
Insulin
Structure
Intracellular domain
Large extracellular binding site
Binding triggers dimerization of receptor

G-Protien Coupled receptors

Sesceptable to desensitization
Clinically, may need to increase dosage over time
Caused by excessive activation of GPCR
Occurs through phosphorylation of cytoplasm tail
May activate or inhibit effector protien
Alpha beta and Gamma subunit
Beta and Gamma subunits may bind targets
upon binding Alpha subunit converts GDP to GTP

Alpha subunit may continue affect effector protein randomly

GTP activates effector protien

Beta and gamma stay bound
Subfamilies
metabotropic glutamate receptor/Ca sensor
Secretin/glucagon
Rhodopsin
7 transmembrane Alpha helicies
Ligand Examples
Opioids
Dopamine
5-HT
ACH

Ligand Gated ion channel

Duration of effect can vary
onset time is equal
Rapid response upon binding
primarily mediate chloride transport
Upon binding, channel changes conformation to allow ions to pass
2 neurotransmitter binding receptors
5 subunit ligand
Receptor Examples
GABA type A receptor
5-hydroxytryptamine type 3 (5-HT3) receptors
Nicotinic ACH receptor