TY - JOUR
T1 - Interaction between the insulin receptor and its downstream effectors
T2 - Use of individually expressed receptor domains for structure/function analysis
AU - Paz, Keren
AU - Voliovitch, Hedva
AU - Hadari, Yaron R.
AU - Roberts, Charles T.
AU - LeRoith, Derek
AU - Zick, Yehiel
PY - 1996/3/22
Y1 - 1996/3/22
N2 - A structural analysis has been carried out to determine which part of the intracellular domain of the insulin receptor (IR) β subunit is involved in direct interaction with the receptor substrates IRS-1 and Shc. Toward this end, the juxtamembrane (JM) domain (amino acids 943-984) and the carboxyl-terminal (CT) region (amino acids 1245-1331) of IR were expressed in bacteria as (His)6-fusion peptides, and their interaction with IRS-1 and Shc was studied. We could demonstrate that the CT region of IR was sufficient to bind Shc, although significant, but much lower binding of Shc to the JM region could be detected as well. Furthermore, in vitro Tyr phosphorylation of the CT region potentiated its interactions with Shc 2-fold. In contrast, the JM region, but not the CT domain of the IR, was sufficient to mediate interactions between the IR and IRS-1. These interactions did not involve the pleckstrin homology (PH) region of IRS-1, since an IRS-1 mutant, in which four "blocks" of the PH domain (Pro5-Pro65) were deleted, interacted with the JM region of IR with the same efficiency as native IRS-1. These results suggest that the ER interacts with its downstream effectors through distinct receptor regions, and that autophosphorylation of Tyr residues located at the CT domain of the IR can modulate these interactions.
AB - A structural analysis has been carried out to determine which part of the intracellular domain of the insulin receptor (IR) β subunit is involved in direct interaction with the receptor substrates IRS-1 and Shc. Toward this end, the juxtamembrane (JM) domain (amino acids 943-984) and the carboxyl-terminal (CT) region (amino acids 1245-1331) of IR were expressed in bacteria as (His)6-fusion peptides, and their interaction with IRS-1 and Shc was studied. We could demonstrate that the CT region of IR was sufficient to bind Shc, although significant, but much lower binding of Shc to the JM region could be detected as well. Furthermore, in vitro Tyr phosphorylation of the CT region potentiated its interactions with Shc 2-fold. In contrast, the JM region, but not the CT domain of the IR, was sufficient to mediate interactions between the IR and IRS-1. These interactions did not involve the pleckstrin homology (PH) region of IRS-1, since an IRS-1 mutant, in which four "blocks" of the PH domain (Pro5-Pro65) were deleted, interacted with the JM region of IR with the same efficiency as native IRS-1. These results suggest that the ER interacts with its downstream effectors through distinct receptor regions, and that autophosphorylation of Tyr residues located at the CT domain of the IR can modulate these interactions.
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U2 - 10.1074/jbc.271.12.6998
DO - 10.1074/jbc.271.12.6998
M3 - Article
C2 - 8636129
AN - SCOPUS:0029924172
SN - 0021-9258
VL - 271
SP - 6998
EP - 7003
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 12
ER -