Please find below your explanation. If I summarize your
answer that clathrin plays major role for secretary and endocytosis
however adaptin plays role with clathrin.
Clathrin role in secretary: a second class of
coat proteins that form a layer between the clathrin and the
membrane
The secretory pathway in eukaryotic cells is used to send
proteins and lipids to the plasma membrane and certain
membrane-bound organelles and to release material outside the cell.
There are two types of secretion: constitutive and regulated.
Constitutive secretion is the default pathway and is used primarily
to replenish material at the plasma membrane and certain
membrane-bound organelles. Regulated secretion terminates in
secretory vesicles that store secreted material until a signal
triggers fusion with the plasma membrane. Both types of secretion
use the same pathway but signal sequences divert proteins into the
regulated pathway. Cells also retrieve material from the plasma
membrane through
- Clathrin forms the coat around vesicles, and the vesicles
accumulate lysosomal proteins before budding from the trans-Golgi
network. These vesicles fuse with endosomes. The lumen of endosomes
has a low pH causing the mannose 6-phosphate receptor to dissociate
from lysosomal proteins. The mannose 6-phosphate receptor is
returned to the trans-Golgi network and the vesicle containing the
lysosomal proteins matures into a functional lysosome.
- Some proteins are sorted into secretory vesicles that store
these proteins until the cell is signaled to release them. The
mechanism of by which proteins are sorted into secretory vesicles
as these proteins do not share a common sorting signal
sequence.
Clathrin role in Endocytosis:
Cells not only release material to the external environment but
they also take up material from outside the plasma membrane through
endocytosis. There are several forms of endocytosis.
- Phagocytosis allows some cells (macrophages, neutrophils) to
engulf and take up large particles such as microorganisms and dead
cells. Phagocytosis involves the protrusion of the plasma membrane
around the particle. Protrusion is driven by actin polymerization.
The plasma membrane eventually surrounds the particle and fuses to
completely enclose it and form a large endocytic vesicle.
- Pinocytosis forms much smaller vesicles (~ 100 nm) and allows
cells to take up small amounts of extracellular fluid and portions
of the plasma membrane. One form of pinocytosis is
clathrin-mediated endocytosis that allows cells to take up specific
proteins from the cell surface.
Clathrin-mediated endocytosis begins with the formation of pit
in the plasma membrane. The pit is surrounded on the cytoplasmic
side by adaptor proteins that link clathrin to the pit. The
adaptors also interact with proteins in the plasma membrane that
are targeted for endocytosis. The pit can accommodate ~ 1000
proteins. Polymerization of clathrin drives formation of a vesicle
that eventually pinches off from the plasma membrane. The GTPase
dynamin catalyzes the pinching off reaction. The clathrin-coated
vesicles fuse with endosomes where the low pH dissociates ligands
from receptors. Some proteins are then returned to the plasma
membrane whereas others are targeted to the lysosome where they are
degraded.
Adaptin role:
- Clathrin adaptor proteins, also known as adaptins, are proteins
that mediate the formation of vesicles for intracellular
trafficking and secretion. Adaptins are clustered subunits of
adaptor protein (AP) complexes.There are several types of adaptin,
each related to a different AP complex.
- Clathrin molecules seem to be specific for certain receptors.
The way that specificity is achieved is through the use of a
molecule called adaptin. The cytoplasmic side of individual
receptors may bind to specific adaptin molecules, which are bound
to clathrin. This chain of associations can give specificity to
clathrin-coated pits, meaning that specific receptors can be
endocytosed into one pit. In some cases, receptors are endocytosed
whether they have bound a ligand or not. In other cases, the only
time that the receptor takes on a conformation that is amenable to
binding adaptin is after the receptor has bound its specific
ligand.