protein-coupled receptor family that has
a characteristic seven transmembrane
domain structure (Fig. 4.7). To date, the
presence of three unique receptors has
been confirmed with the cloning of the
1-, 2- and 3-adrenergic receptor genes
in several species (Table 4.7). Homology
among the receptor subtypes is relatively
low (30–50%), with conserved amino
acids primarily restricted to the seven
transmembrane domain segments and
membrane-proximal regions of the intra-
cellular loops (Fig. 4.7). Despite these
differences among receptor subtypes,
amino acid sequences of individual sub-
types are highly conserved across species.
For example, the 3-adrenergic receptor
is 80–90% conserved across human,
mouse, rat, canine and bovine amino acid
sequences (see Table 4.7 for references).
The transmembrane domains of the -
adrenergic receptors have been implicated
in receptor subtype-specific ligand binding.
A series of 1–2-adrenergic receptor
chimeras was produced by Marullo et al.
(1995) to study the role of the trans-
membrane domains in ligand binding.
These authors concluded that receptor
specificity is determined by unique inter-
actions among agonists and several trans-
membrane domains. More recently,
individual transmembrane domains of the
1- and 2-adrenergic receptors were
exchanged to evaluate the role of each
domain individually (Kikkawa et al., 1998;
Kurose et al., 1998). Transmembrane
domains 2 and 7 were implicated in
affinity for the 2-adrenergic receptor,
while transmembrane domain 2 was
critical for 1-adrenergic receptor affinity.
Phenethanolamine Repartitioning Agents 79
Fig. 4.7.Primary structure of the 1-adrenergic receptor. The amino acid sequence of the human 1-
adrenergic receptor is represented by the one-letter code for amino acids. The polypeptide chain is arranged
according to the model for rhodopsin. Shaded amino acids are conserved across the human 1-, 2- and
3-adrenergic receptors (31% of residues). Amino acids in circles are conserved across the 1-adrenergic
receptor of humans, pigs and sheep (80% of residues; see Table 4.7 for references). Transmembrane domains
are labelled in parentheses.
RLQT
AIA
IV
N L
G V
LV
W
T
N
F
LS
A
ADL
MV
GL V
PV
A
G
CE
TW
S
DV
VCL
TA
EIS
TL
C
A
RD
Y
A
T
P Y
L
T
AR
WV
S
SE
R
Y
V
IP
V
LP
SV
SS
F
A
Q
RR
F
FY
W
M
N
A
C C
C
F
F
E
R
Y
L
L
MI
F
N
P
WCL
L
L
N
NW
A
F
G
G T
T
G
L
E
L G N F P Y C F
I
RS
S
P R A
Y
D F
LLC
FR
04 Farm Animal Metabolism 04 20/4/00 12:02 pm Page 79