Biology
KEY CONCEPTS:
A surprising property of anchor sequences is that they can function as signal sequences when engineered into a different location. When placed into a protein lacking other signals, such a sequence may sponsor membrane translocation. One possible explanation for these results is that the signal sequence and anchor sequence interact with some common component of the apparatus for translocation. Binding of the signal sequence initiates translocation, but the appearance of the anchor sequence displaces the signal sequence and halts transfer.
Type II proteins do not have a cleavable leader sequence at the N-terminus. Instead the signal sequence is combined with an anchor sequence. We imagine that the general pathway for the integration of type I proteins into the membrane involves the steps illustrated in Figure 8.34. The signal sequence enters the membrane, but the joint signal-anchor sequence does not pass through. Instead it stays in the membrane (perhaps interacting directly with the lipid bilayer), while the rest of the growing polypeptide continues to loop into the endoplasmic reticulum.
- Proteins Reside In Membranes By Means Of Hydrophobic Regions
KEY TERMS:The transmembrane region (transmembrane domain) is the part of a protein that spans the membrane bilayer. It is hydrophobic and in many cases contains approximately 20 amino acids that form an ?-helix. It is also called the transmembrane...
- Translocation Requires Insertion Into The Translocon And (sometimes) A Ratchet In The Er
KEY CONCEPTS:The ribosome, SRP, and SRP receptor are sufficient to insert a nascent protein into a translocon. Proteins that are inserted post-translationally require additional components in the cytosol and Bip in the ER. Bip is a ratchet that prevents...
- The Translocon Forms A Pore
KEY TERMS:A translocon is a discrete structure in a membrane that forms a channel through which (hydrophilic) proteins may pass. KEY CONCEPTS: The Sec61 trimeric complex provides the channel for proteins to pass through a membrane. A translocating protein...
- The Signal Sequence Interacts With The Srp
KEY TERMS:Protein translocation describes the movement of a protein across a membrane. This occurs across the membranes of organelles in eukaryotes, or across the plasma membrane in bacteria. Each membrane across which proteins are translocated has a...
- Signal Sequences Initiate Translocation
KEY TERMS:Protein sorting (targeting) is the direction of different types of proteins for transport into or between specific organelles. A signal sequence is a short region of a protein that directs it to the endoplasmic reticulum for co-translational...
Biology
Anchor sequences determine protein orientation
KEY TERMS:
- An anchor (stop-transfer) (often referred to as a "transmembrane anchor") is a segment of a transmembrane protein which resides in the membrane.
- An anchor sequence halts the passage of a protein through the translocon. Typically this is located at the C-terminal end and results in a group I orientation in which the N-terminus has passed through the membrane.
- A combined signal-anchor sequence can be used to insert a protein into the membrane and anchor the site of insertion. Typically this is internal and results in a group II orientation in which the N-terminus is cytosolic.
Proteins that are secreted from the cell pass through a membrane while remaining in the aqueous channel of the translocon. By contrast, proteins that reside in membranes start the process in the same way, but then transfer from the aqueous channel into the hydrophobic environment. The challenge in accounting for insertion of proteins into membranes is to explain what distinguishes transmembrane proteins from secreted proteins, and causes this transfer. The pathway by which proteins of either type I or type II are inserted into the membrane follows the same initial route as that of secretory proteins, relying on a signal sequence that functions co-translationally. But proteins that are to remain within the membrane possess a second, stop-transfer signal. This takes the form of a cluster of hydrophobic amino acids adjacent to some ionic residues. The cluster serves as an anchor that latches on to the membrane and stops the protein from passing right through.
Membrane insertion starts by the insertion of a signal sequence in the form of a hairpin loop, in which the N-terminus remains on the cytoplasmic side. Two features determine the position and orientation of a protein in the membrane: whether the signal sequence is cleaved; and the location of the anchor sequence.
The insertion of type I proteins is illustrated in Figure 8.33. The signal sequence is N-terminal. The location of the anchor signal determines when transfer of the protein is halted. When the anchor sequence takes root in the membrane, domains on the N-terminal side will be located in the lumen, while domains on the C-terminal side are located facing the cytosol.
A common location for a stop-transfer sequence of this type is at the C-terminus. As shown in the figure, transfer is halted only as the last sequences of the protein enter the membrane. This type of arrangement is responsible for the location in the membrane of many proteins, including cell surface proteins. Most of the protein sequence is exposed on the lumenal side of the membrane, with a small or negligible tail facing the cytosol.
Type II proteins do not have a cleavable leader sequence at the N-terminus. Instead the signal sequence is combined with an anchor sequence. We imagine that the general pathway for the integration of type I proteins into the membrane involves the steps illustrated in Figure 8.34. The signal sequence enters the membrane, but the joint signal-anchor sequence does not pass through. Instead it stays in the membrane (perhaps interacting directly with the lipid bilayer), while the rest of the growing polypeptide continues to loop into the endoplasmic reticulum.
The signal-anchor sequence is usually internal, and its location determines which parts of the protein remain in the cytosol and which are extracellular. Essentially all the N-terminal sequences that precede the signal-anchor are exposed to the cytosol. Usually the cytosolic tail is short, ~6-30 amino acids. In effect the N-terminus remains constrained while the rest of the protein passes through the membrane. This reverses the orientation of the protein with regard to the membrane.
The combined signal-anchor sequences of type II proteins resemble cleavable signal sequences. Figure 8.35 gives an example. Like cleavable leader sequences, the amino acid composition is more important than the actual sequence. The regions at the extremities of the signal-anchor carry positive charges; the central region is uncharged and resembles a hydrophobic core of a cleavable leader. Mutations to introduce charged amino acids in the core region prevent membrane insertion; mutations on either side prevent the anchor from working, so the protein is secreted or located in an incorrect compartment.
The distribution of charges around the anchor sequence has an important effect on the orientation of the protein. More positive charges are usually found on the cytoplasmic side (N-terminal side in type II proteins). If the positive charges are removed by mutation, the orientation of the protein can be reversed. The effect of charges on orientation is summarized by the "positive inside" rule, which says that the side of the anchor with the most positive charges will be located in the cytoplasm. The positive charges in effect provide a hook that latches on to the cytoplasmic side of the membrane, controlling the direction in which the hydrophobic region is inserted, and thus determining the orientation of the protein.
- Proteins Reside In Membranes By Means Of Hydrophobic Regions
KEY TERMS:The transmembrane region (transmembrane domain) is the part of a protein that spans the membrane bilayer. It is hydrophobic and in many cases contains approximately 20 amino acids that form an ?-helix. It is also called the transmembrane...
- Translocation Requires Insertion Into The Translocon And (sometimes) A Ratchet In The Er
KEY CONCEPTS:The ribosome, SRP, and SRP receptor are sufficient to insert a nascent protein into a translocon. Proteins that are inserted post-translationally require additional components in the cytosol and Bip in the ER. Bip is a ratchet that prevents...
- The Translocon Forms A Pore
KEY TERMS:A translocon is a discrete structure in a membrane that forms a channel through which (hydrophilic) proteins may pass. KEY CONCEPTS: The Sec61 trimeric complex provides the channel for proteins to pass through a membrane. A translocating protein...
- The Signal Sequence Interacts With The Srp
KEY TERMS:Protein translocation describes the movement of a protein across a membrane. This occurs across the membranes of organelles in eukaryotes, or across the plasma membrane in bacteria. Each membrane across which proteins are translocated has a...
- Signal Sequences Initiate Translocation
KEY TERMS:Protein sorting (targeting) is the direction of different types of proteins for transport into or between specific organelles. A signal sequence is a short region of a protein that directs it to the endoplasmic reticulum for co-translational...