Regulation of β2-adrenergic receptor function by conformationally selective single-domain intrabodies

TY - JOUR

T1 - Regulation of β2-adrenergic receptor function by conformationally selective single-domain intrabodies

AU - Staus, Dean P

AU - Wingler, Laura M

AU - Strachan, Ryan T

AU - Rasmussen, Søren Gøgsig Faarup

AU - Pardon, Els

AU - Ahn, Seungkirl

AU - Steyaert, Jan

AU - Kobilka, Brian K

AU - Lefkowitz, Robert J

PY - 2014/3

Y1 - 2014/3

N2 - The biologic activity induced by ligand binding to orthosteric or allosteric sites on a G protein-coupled receptor (GPCR) is mediated by stabilization of specific receptor conformations. In the case of the b2 adrenergic receptor, these ligands are generally small-molecule agonists or antagonists. However, a monomeric single-domain antibody (nanobody) from the Camelid family was recently found to allosterically bind and stabilize an active conformation of the b2-adrenergic receptor (b2AR). Here, we set out to study the functional interaction of 18 related nanobodies with the b2AR to investigate their roles as novel tools for studying GPCR biology. Our studies revealed several sequence-related nanobody families with preferences for active (agonist-occupied) or inactive (antagonist-occupied) receptors. Flow cytometry analysis indicates that all nanobodies bind to epitopes displayed on the intracellular receptor surface; therefore, we transiently expressed them intracellularly as "intrabodies" to test their effects on b2AR-dependent signaling. Conformational specificity was preserved after intrabody conversion as demonstrated by the ability for the intracellularly expressed nanobodies to selectively bind agonist-or antagonist-occupied receptors. When expressed as intrabodies, they inhibited G protein activation (cyclic AMP accumulation), G protein-coupled receptor kinase (GRK)-mediated receptor phosphorylation, b-arrestin recruitment, and receptor internalization to varying extents. These functional effects were likely due to either steric blockade of downstream effector (Gs, b-arrestin, GRK) interactions or stabilization of specific receptor conformations which do not support effector coupling. Together, these findings strongly implicate nanobody-derived intrabodies as novel tools to study GPCR biology.

AB - The biologic activity induced by ligand binding to orthosteric or allosteric sites on a G protein-coupled receptor (GPCR) is mediated by stabilization of specific receptor conformations. In the case of the b2 adrenergic receptor, these ligands are generally small-molecule agonists or antagonists. However, a monomeric single-domain antibody (nanobody) from the Camelid family was recently found to allosterically bind and stabilize an active conformation of the b2-adrenergic receptor (b2AR). Here, we set out to study the functional interaction of 18 related nanobodies with the b2AR to investigate their roles as novel tools for studying GPCR biology. Our studies revealed several sequence-related nanobody families with preferences for active (agonist-occupied) or inactive (antagonist-occupied) receptors. Flow cytometry analysis indicates that all nanobodies bind to epitopes displayed on the intracellular receptor surface; therefore, we transiently expressed them intracellularly as "intrabodies" to test their effects on b2AR-dependent signaling. Conformational specificity was preserved after intrabody conversion as demonstrated by the ability for the intracellularly expressed nanobodies to selectively bind agonist-or antagonist-occupied receptors. When expressed as intrabodies, they inhibited G protein activation (cyclic AMP accumulation), G protein-coupled receptor kinase (GRK)-mediated receptor phosphorylation, b-arrestin recruitment, and receptor internalization to varying extents. These functional effects were likely due to either steric blockade of downstream effector (Gs, b-arrestin, GRK) interactions or stabilization of specific receptor conformations which do not support effector coupling. Together, these findings strongly implicate nanobody-derived intrabodies as novel tools to study GPCR biology.

KW - Amino Acid Sequence

KW - Cell Line

KW - Cyclic AMP

KW - G-Protein-Coupled Receptor Kinases

KW - HEK293 Cells

KW - Humans

KW - Molecular Sequence Data

KW - Phosphorylation

KW - Protein Binding

KW - Receptors, Adrenergic, beta-2

KW - Receptors, G-Protein-Coupled

KW - Sequence Alignment

KW - Single-Domain Antibodies

U2 - 10.1124/mol.113.089516

DO - 10.1124/mol.113.089516

M3 - Journal article

C2 - 24319111

SN - 0026-895X

VL - 85

SP - 472

EP - 481

JO - Molecular Pharmacology

JF - Molecular Pharmacology

IS - 3

ER -