15.6
Translocación de proteínas cotraduccional
La translocación de proteínas a través de membranas es un proceso antiguo que ocurre incluso en bacterias y arqueobacterias. De hecho, los componentes…
La mayoría de las proteínas ingresan a la luz del RE mientras aún están en síntesis, un proceso llamado translocación cotraduccional.
En primer lugar, el complejo receptor SRP-SRP que transporta el complejo de cadena naciente ribosoma lo descarga en el canal Sec61.
Una vez que el ribosoma se alinea con el canal, la secuencia de señal en el terminal N de la cadena polipeptídica se engancha en un sitio de reconocimiento de secuencia de señal.
A medida que la traducción continúa, la cadena polipeptídica forma un bucle que abre el tapón del canal para entrar en el lumen del RE.
Mientras el polipéptido desciende al lumen, la secuencia de señal sale a través de la puerta lateral del canal Sec61 para entrar en el complejo de peptidasa señal adyacente, donde se escinde.
El tapón del canal permanece abierto a medida que la proteína desciende pasivamente hacia el lumen del RE.
Después de la translocación completa de la proteína en el lumen, el tapón del canal rebota para bloquear el regreso de la proteína al citosol.
Dentro del lumen del RE, las chaperonas residentes del RE, como BiP, se unen inmediatamente a la proteína translocada y ayudan en el plegamiento de la proteína.
View the full transcript and gain access to JoVE Core videos
Q1: What is cotranslational protein translocation and how does it differ from other translocation methods?
Cotranslational protein translocation occurs while proteins are still being synthesized by ribosomes. The nascent polypeptide chain enters the ER lumen during translation, contrasting with post-translational translocation of proteins to the RER, where proteins are fully synthesized before translocation. This simultaneous synthesis and translocation process is mediated by the SRP-SRP receptor complex and the Sec61 channel.
Q2: How does the Sec61 channel facilitate protein entry into the ER lumen?
The Sec61 channel contains a plug that blocks the channel opening. When the signal sequence of the nascent polypeptide latches onto a recognition site, it pushes the plug open, creating an entry pathway. As translation continues, the polypeptide descends passively through the channel into the ER lumen. After translocation completes, the channel plug bounces back to seal the channel and prevent protein return to the cytosol.
Q3: What role does the signal sequence play in cotranslational translocation?
The signal sequence at the N-terminal of the nascent polypeptide chain recognizes and latches onto a specific signal sequence recognition site on the Sec61 channel. This interaction triggers channel opening and initiates translocation. The signal sequence then exits through the lateral gate of the Sec61 channel to enter the signal peptidase complex, where it is cleaved off during translocation.
Q4: What are the key protein components that work with the Sec61 channel during cotranslational translocation?
The signal recognition particle (SRP) and SRP receptor (SR) deliver the ribosome-nascent chain complex to the Sec61 channel through GTP hydrolysis. Accessory proteins like the translocon-associated protein (TRAP) complex stabilize weak signal sequences, while the TRAM protein acts as a chaperone assisting in folding and membrane integration of translocating proteins.
Q5: How do ribosomes contribute to protein movement through the Sec61 channel?
Ribosomes act as primary translocation motors, pushing the nascent polypeptide chain toward the ER lumen during translation elongation. The ribosome aligns with the Sec61 channel, and as peptide bonds form, the growing polypeptide is propelled through the channel. This process requires no additional energy beyond the GTP hydrolysis used for normal peptide chain elongation.
Q6: What happens to proteins after they complete translocation into the ER lumen?
Once the polypeptide fully enters the ER lumen, the Sec61 channel plug closes to prevent protein return to the cytosol. Resident ER chaperones, particularly BiP, immediately bind the translocated protein and assist in proper protein folding. This quality control mechanism ensures proteins achieve their correct three-dimensional structure within the ER environment.
Q7: Why is the TRAP complex essential for proteins with low-hydrophobicity signal sequences?
The TRAP complex is a substrate-specific auxiliary component that stabilizes signal sequences with weak hydrophobic interactions. It directly interacts with the Sec61 channel and maintains the channel in an open conformation, compensating for the reduced binding strength between the signal sequence and the channel. This ensures secure anchoring and successful translocation of these challenging substrates.