BIOCHEMICAL
Vol. 55, No. 3, 1973
BLOOD-GROUP
ACTIVITY
AND BIOPHYSICAL RESEARCH COMMUNICATIONS
OF HUMAN CHORIONIC
GONADOTROPIN
L. M&z, 0. P. Bahll Department of Biochemistry J. of Microbiology,
Department
Received
and F. Mohnl Blood-Group
State
School University Buffalo,
September
25,1973
Research
Unit
of Medicine of New York at Buffalo N. Y. 14214
SUMMARY Human Chorionic blood-group tion. in
A-like
inhibition the
Gonadotropin activity
of
.A11 of
the
hormone
contain
any N-acetylgalactosamine,
for
blood-group
the
comprised
(hCG-a
and hCG-6)
15,000
and 23,000,
in
of
D-galactose, acid
(hCG) is
two noncovalently
with
approximate
respectively
subunits
The carbohydrate
(l-4).
it
is does
a component
located
not
necessary
molecular .and each
have moiety
been of
subunits weights
containing
and amino recently
hCG-a
N-acetyl-D-glucosamine
D-mannose,
a glycoprotein
bonded
The monosaccharide both
hemagglutina-
activity
although
Gonadotropin
30% carbohydrate. sequences
the
to have
A activity.
Human Chorionic hormone
found
as shown by the
technique.
a subunit
has been
about acid
established
is made up of and sialic
while that of hCG-6 contains N-acetyl-D-galactosamine This work was supported in part by U. S. Public 1.
Health Population
Service
Grants
Council
AM10273
and HEO5351,
of New York. 717
Copyright 0 1973 by Academic Press, Inc. All rights of reprqduction in any form reserved.
of
and by the
BIOCHEMICAL
Vol. 55, No. 3, 1973
and L-fucose,
in
Furthermore,
addition
the
in the
RESEARCH COMMUNICATIONS
above
part
monosaccharides.
of
features linkages,
the
resembles
mucins
In
on the
proteins
on the
prompted
an examination activities.
this
This
are
the
hormone
and the
serum
structural
the
molecule
glyco-
for
various
presents
and their
prese::t
considerations
communication
such an investigation
serine respect
These of
as two types
N-acetylglucosaminyl
one hand
other.
hCG-$ molecule
inasmuch
and N-acetylgalactosaminyl same molecule.
group
the
structural
carbohydrate-protein
asparagine
of
to
carbohydrate
has some unusual of
AND BIOPHYSICAL
possible
blood-
the
results
physiological
significance. MATERIALS
AND METHODS
Highly
purified
described units
samples
(5) were
of hCG prepared
employed
in
of hCG were prepared
with
8 M urea
followed
A-50
and Sephadex
(LH) was kindly acid
studies.
The sub-
by dissociation
of
by chromatography
G-100
(8,2).
supplied
glycoprotein
these
as previously
luteinizing
Papkoff.
were purified
hormone
on DEAE-Sephadex
Ovine
by Dr.
the
hormone
Fetuin
by published
and ol-
procedures
(6,7).
Determination Serial
(9): buffered (w/v)
of twofold
saline of each
an equal
volume
or lectin
just
ate
3% PBS cell
carried
out
ABH and Lewis serologic
solution, substance
pH 7.35 under
immediately
in
(PBS)
of
examination
maximum
suspensions
group
dilutions
oc one pre-selected causing
blood
in
prior
718
were mixed
agglutination
to
preliminary each
phosphate 1% solutions
dilution
the
activities
assay.
with
of
antiserum
of
approprititration
The sub-
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Vol. 55, No. 3,1973
stance-antibody ture
for
15 minutes
minutes were
mixtures
for
incubated temperature
In
examinations
properties,
a lectin
a simple
group of
saline gorse)
Any A-like immune)
0 secretor
activity
1% solutions and group controls.
of porcine
cells
with
group
B salivas. a human
controls
human
Le(a-b+)
and Le(a-b-).
RESULTS
AND DISCUSSION
Lewis tion
blood-group technique.
salivas
of
activities The hormone
salivas
inac-
salivas
as
was determined serum
and group
B
was examined cells
using
as
Le(a+b-),
was examined
719
(non-
and nonsecretor
phenotypes
showed
(9).
Al
activity
by the
al.
and human group
and Le(a+b-)
Gonadotropin
samples
with
secretor
the
single
AZ erythrocytes
anti-B
blood-group serum
was used with
a natural
property
human
of human Lewis
Human Chorionic
and group
as
europaeus
by Mohn --et
A substances
(nonimmune)
anti-Lea
Ulex
of
using
any B-like
controls
prepared
(10)
and nonsecretor
Similarly
a natural
with
serum
A2 secretor
agglutination.
and nonsecretor
was detected
anti-A
of
consisted
as reported
at
inhibitory
previously
The controls
human
seeds
were
centrifugation
specificity
the
tubes at room
macroscopic
anti-H of
and clarified
30 minutes
H antigen-like
as described
0 cells.
tivated
with
extract
human group
with
for
cells
the
following for
and 30
detector
contents,
15 or
read
tempera-
ABH inhibitions
their
and,
were
at room
appropriate
an additional
3 min,
the
(common
mixing
accordingly
600 g for
for
and then
After for
incubated
in tests
Lewis,
added.
were
for
hemagglutination a significant
A,B,H
and inhibi-
cross-reac-
4 f
2 P
(11
+t
++++ +++ +++ tt +t
33rl
&
++++ +++t ++++ +t+ +t
++++ +++t ++++ ++-I-+ +++t
Cl
+t++ +++ ++ +t
++++ ++++ ++++ -I-+++ +++t
sasuezpqns
LPT-Sfl
++++
Q
aurarod
600-S3
++++
as
&
++
++++ +++t ++++ +++ ++t
ZQ dno;cs
++++ t++t +4-t+ t+t+ t-t++ +++t +ttt
+t++ +t+t +ttt +++t ++t+
SPAJ'IBS
as
A
+++t +tt ++t tt
IQ dnoxg
as
++++ ++++ t+++ ++++ ++++ ++++ ++tt
++++ +tt+ t+++ ttt+ +t+t
8ZT:T v9:'I ZEET g-c:1 8:T tr:-E z:T
auras P-LOT :'I ITS:1 9SZZT
= as
= as
pa3n~rtwn
zoqaxoas
zoziamasuou
Vol. 55, No. 3,1973
tivity
with
almost
all
BIOCHEMICAL
blood-group of
the
and,
on a weight
than
in
the
the
f3 subunit
conditions human
blood-group hCG used
these
all
which
does
mine,
a necessary
of
the
not
Blood-group
not
studies
component is
(12)
to this
contain
with
the
present
in
hCG-a.
Since
inhibit
the
ally
appears the sary
that
possible
the
this
the
unit
A substance. with but
nonthere
to a recent
(CEA) of
was found
the
human
to possess
A-like
any N-acetylgalactosamine of
the
mannose
these
of
antigen
are
monosaccharides
structure impart
cross-reactivity
the with
also
individu-
reaction, of the
were
and L-fucose
L-fucose,
hemagglutination
must
since
a subunit
according
exception
overall
carbohydrate for
rule
N-acetylglucosamine,
do not
in
components
which,
of
N-acetylgalactosa-
antigen
acid,
and
Further-
(ll).,
sialic
serum,
purified.
N-acetylgalactosamine
not
in
hCG preparations
associated
The monosaccharide
l
in
The antigen
and did
activity
fetal
generally
system.
a subunit
assay
of blood-group
on carcinoembryonic
digestive
the
be due to any contaminant
any detectable
A activity
u subuni‘t
show any activity.
was located
contain
the
similar
was highly
activity
terminal
not
Furthermore,
The activity
bovine
present
seems to be exceptions report
from did
could
more,
reducing
fetuin
A substance in
in in
I).
Under
glycoprotein
activity
resided
(Table
was negligible.
al-acid
I).
was much greater
hormone
LH,
RESEARCH COMMUNICATIONS
(Table
activity
basis,
ovine
This
A substance
A-like
intact
AND BIOPHYSICAL
whole
it or part
conformation
blood-group
necesA
substance. Although the
structural
more
work
components
is
needed required
721
to determine for
the
precisely A-like
activity,
of
BIOCHEMICAL
Vol. 55, No. 3, 1973
the
carbohydrate
the
serological
in
the
are since
activity.
located the
hCG with its
of hCG-cr does
hCG-anti-hCG
not
in
sequential
binding
the
Also,
least
part
of
the
the
been of
potentially postulated
sion
of
the
lymphocytes hormone
not
that not
of
the
very
molecule,
the
from
much alter by radio-
carbohydrate,
necessary
its
that
determinants
as determined
is
for
testicular
at
the
and ovarian
significance but
during
endometrium
by the
immunoresponse
has been
in view of
of
The question
which
those
of
is fetal the
by binding
to
exhibit
the
in
fetus has
acceptance
mother.
with that
the
antigens
be involved
be noted
present
fascinating
implantation
the
found
the
suppression
since
hCG might
may
of
biologists
from
It
is
the
(13).
mother
that
(13).
it
the
transplantation
which
to note
monosaccharides
does
with
different
been
the
of hCG in
function
fetus
it,
clear,
role
puzzling
the
of
yet
possible
on maternal
of
physiological
is not
lymphocyte
part
with
receptors2.
The precise
of
carbohydrate
appears
hormone
membrane
findings
antigenic
antibody2 it
interesting
the
glycosidases
-with
a major
is
removal
immunoassay.
plasma
the
RESEARCH COMMUNICATIONS
seem to be associated
It
reaction
specific
binding
AND BIOPHYSICAL
are It
the
has suppres-
maternal
hCG is
the
first
blood-group
activity.
2.
Manuscript
in
preparation.
ACKNOWLEDGMENT The authors
wish
to thank
Dr.
suggestions.
722
V. Ginsburg
for
helpful
BIOCHEMICAL
Vol. 55, No. 3,1973
AND BIOPHYSICAL RESEARCH COMMUNICATIONS
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