SPI-Mark™ Colloidal Gold Reagents
How to Get the Best from Immunogold Labelling
All SPI-Mark gold and silver reagents come with detailed technical instructions for correct use in
immunolabelling. Protocols for use are provided together with recommended dilutions,
buffers, blocking reagents, etc. Each product is supplied with a detailed data sheet that
provides information on specification and performance. Our Customer Service Group is always ready to give continuous advice for the use of our reagents with many different applications, including those that are out- of-the-ordinary.
The primary aim of all immunolabelling procedures is to obtain a maximum specific signal with
a minimum non specific background. This is true for EM sections, LM sections, and
immunoblots on membranes. The results obtained in any immunolabelling procedure are
limited mainly by the specimen preparation and incubation procedures. References given here
describe a number of optimum conditions and protocols for immunolabelling in LM, EM and
Blotting applications. Although it is not possible to describe immunolabelling procedures for
every possible application, extra protocols are available on request for basic approaches to
each specimen type. These are described at the end of this page.
Specimen Preparation
Correct specimen preparation procedures are absolutely crucial for optimum labelling of
antigens in cells and tissues. Methods commonly used for ultrastructural preservation in the
EM or morphological preservation in the LM must usually be modified to ensure that antigens
are not only retained but also available for labelling. This often involves compromise with the
structure but careful selection of preparation methods can yield excellent combinations of
structural detail and immunochemical labelling.
Potential loss of antigenicity during microscopical preparation procedures
For LM and EM studies cells and tissue sections may be studied by preembedding, post
embedding, or cryotechniques. In addition whole cells may be examined as cytospins, cell
smears, cells in culture, and cells in suspension 1,2,3,4.
It should be recognised that each step of the preparation procedure is likely to incur some
antigenic loss by extraction or alteration or masking. Cumulatively these losses may greatly
reduce the overall labelling unless each step is optimised. This can usually only be achieved
empirically but some guidelines are described below.
a) Fixation
Cells and tissues may be fixed for subsequent examination or may sometimes be labelled in
the unfixed state. Fixation of the tissue must also preserve antigenicity without compromise to
structural characteristics. Fixatives either denature proteins by coagulation (eg acetone or
methanol) or by forming additive cross linked compounds (eg aldehydes), or both. The
resulting complexes inevitably differ from the unfixed proteins in both their chemical and
antigenic profiles. Each tissue requires its own fixation protocol. For example, too much cross
linking in a tissue with high protein density may mask many antigens. On the other hand a
loose tissue with low protein content may disintegrate without adequate fixation and antigens
may simply be washed out. According to the antibodies employed for antigen detection it
may not be necessary to completely preserve the protein under investigation if at least the
specific antigen is conserved. The types of fixatives employed are shown in the table below.
Types of Fixatives
Structure
Antigen preservation
Suitability
Additive (cross linking)
-Formaldehyde
-Glutaraldehyde
++
+++
++
+
Tissues
Tissues
Coagulative (precipitating)
-Acetone
-Methanol
+
+
+
+
Cells
Cells
Mixed
-Formal acetone
-Picric acid
++
++
+
+
Cells
Tissues
For many tissues the best compromise is a mixture of formaldehyde (eg 2- 4%) for rapid
stabilising with low cross linking, and weak glutaraldehyde (eg 0.1%) for greater structural
preservation. For cytological investigation a precipitating or coagulating fix such as acetone or
methanol may be preferred. Formal acetone has also been commonly used for fixing cell
preparations. In some cases for cell studies simple air drying may allow enough antigenic
preservation for immunolabelling.
Post fixation for electron microscopy has mostly involved the use of osmium tetroxide in
order to preserve membrane components and provide image contrast. The introduction of
osmium into tissue is not always desirable, however, and more recently tannic acid has been
suggested as an alternative5.
Whatever method of fixation is selected it must serve the dual
function of retaining the essential structural and antigenic components of the tissue without
introducing any material which may interfere with the labelling. In some cases the introduction
of heavy metals such as osmium or uranium into the tissue may cause increased non specific
labelling and must be treated with caution.
b) Washing
Thorough washing of the tissues following fixation is extremely important. It may be necessary
to wash for at least as long as the tissue has been fixed in order to remove excess aldehyde
or other fixation residues which may cause non specific labelling. In some cases quenching the
tissue with ammonium chloride is performed to neutralise aldehyde groups . The wash is best
performed in a buffer having a tonicity similar to the natural tissue state.
c) Embedding
Tissues may be embedded in paraffin wax for LM, and resin for LM or EM studies. In either
case the embedding should allow good preservation of the antigens without sacrifice of
structural information. Generally there are two types of resin, epoxy resins which have an
aromatic structure and are strongly cross linked, and acrylic resins which have lower cross
linking. Epoxy resins are hydrophobic whereas acrylic resins may be hydrophobic or
hydrophilic. The best structural preservation and stability is provided by epoxy resins while
the best immunolabelling is usually achieved with acrylic resins. This is because acrylic resins
cut in such a way as to reveal the proteins at the section surface and they also wet more
easily, thus giving greater accessibility to the antibodies during subsequent incubations.
Resins for EM and LM preparation
Types of resin
Cross
linking
Hydrophilicity
Structure/stability
Antigenic
preservation/access
Epoxy
Araldite
Epon
High
High
Hydrophobic
Hydrophobic
+++
+++
+
+
Acrylic
UNICRYL
LowicrylŽ
LR White
LR Gold
Methacrylate
-
-
-
-
-
Hydrophilic
Hydrophilic
Hydrophilic
Hydrophilic
+/- Hydrophilic
++
++
++
++
+
+++
++
++
++
+
For the optimum results a compromise must be reached and the usual choice is of a polar
(hydrophilic) resin with moderate cross linking. A popular acrylic resin formulation is given by
UNICRYL,
which gives excellent immunolabelling characteristics together with a high degree
of stability and structural preservation. UNICRYL, in common with many other acrylic resins,
also allows the embedding procedure to be performed at low temperatures. This ensures that
vital components are not extracted during dehydration and that no excessive temperature rise
occurs during polymerisation which may damage the tissue antigens.
d)Blotting
For proteins blotted onto membranes by Western blotting or dot blotting it is important to
ensure complete transfer of the proteins to the membrane. Membranes must then be blocked
with neutral proteins or surfactants (eg BSA or Tween 20) to fill unoccupied sites and
prevent non specific background labelling. The membranes are then incubated in a similar
fashion to tissue sections. The complete protein band/spot pattern may first be revealed by
immersing the membrane in a solution of PROTOGOLD which stains all proteins with
colloidal gold, yielding a red stain. This gives an indication of the location of all protein bands.
(See Protogold Section) A second identical membrane may then be incubated with the
appropriate specific antibodies for identification of specific proteins immobilised on the
membrane. An incubation of the membrane with gold labelled second antibodies will reveal
the presence of specific protein bands by a visible red colour where the gold particles
accumulate. In order to achieve the best signal with the least background thorough washing is
important after each step.
Possible sources of non specific labelling
Incubations
In order to achieve the highest possible specific signal with the lowest possible non specific
background it is important to be aware of all the factors in both specimen preparation and in
subsequent incubations which can affect these results. The figure below indicates some of the
most common sources of non specific background that can be identified by the use of
controls and successfully eliminated. These factors apply for all types of tissues, whether for
EM or LM, and for immunoblots on membranes.
a) Primary antibody
The primary antibody should be of high titre and of the highest specific purity to allow the
greatest possible dilution. Cross reactivity must be low, especially with the sample tissue. A
low quality primary antibody is the greatest cause of low specific signal and high background
during the labelling procedure. The buffer composition and pH is important for the
incubations. A normal TBS or PBS buffer is usually chosen with suitable additions to maintain
low background (see below). The specimen must be washed thoroughly with buffer between
incubations.
Typical dilution protocol for determining optimum signal to background labelling
Primary
antibody
Secondary antibody
(gold)
Specific
signal
Non specific
background
Series 1
1/100
1/1000
1/10000
1/100
1/100
1/100
++++
+++
+
++
+
-
Series 2
1/1000
1/1000
1/1000*
1/50
1/100
1/200*
++++
+++
+++
++
+
-
*Resulting optimum conditions for incubation.
(b) Secondary antibody
A high quality second antibody is essential to label the primary specifically and with low
background. SPI-Mark gold conjugates are affinity purified and of the highest quality. They are
provided suspended in Tris or phosphate buffered saline for microscopical or immunoblotting
use with sodium azide preservative and are stable for years under the correct storage
conditions. This because our gold conjugates contain no free antibody, all antibodies being
securely adsorbed at the surface of the gold. In addition the very high proportion of singlets
ensures that clusters will not form in time during storage.
Their high titre and purity means that for incubations they may be used highly diluted (typically
1/100 - 1/400) in the typical incubating buffer shown below, so reducing non specific
background whilst achieving a high signal intensity. Even at high dilutions (1/1000 or more)
the conjugates are extremely stable and may be left for long term incubations.
(c) Dilutions
When establishing a new protocol it is necessary to determine the optimum concentrations of
both the primary and the gold labelled secondary antibodies. This is done by first incubating
separate sections with various dilutions of the primary antibody over an appropriate range of
values, eg 1/100 to 1/10,000. The various primary incubations are then followed by second
incubations, using a constant dilution such as 1/100 of the gold labelled secondary antibody.
The dilution of primary antibody giving the optimum signal and background is thus
determined. The procedure is then repeated, this time using the determined dilution of the
primary as a constant, and incubating with a selected range of dilution values of the gold
conjugate, eg 1/10 to 1/400. Observation of the second set of results will indicate the choice
of dilution of conjugate that should be used in further experiments. The table below gives an
illustration of a typical routine for these dilution series.
With both primary and secondary incubations a greater sensitivity may also be achieved by
agitating the sample or flushing the reagents, so bringing fresh solution continuously to the
target proteins at the tissue surface. If the antibody solutions are tolerant the incubations may
also be performed at slightly elevated temperatures (up to 37C).
c) Blocking
Non specific reactive sites on tissues and cell surfaces as well as unoccupied sites within
blotting membranes may need blocking before antibodies are applied to the specimens. The
causes of non specific labelling may arise from sources shown in the table below. Each
background source will need its own blocking procedure either before or during the antibody
incubations as shown in the table and as described in the BBI Technical Information Booklet
supplied with each product. Blocking reagents are supplied by BBI and are listed separately
in Blocking Reagents Section.
Typical sources of background in immunolabelling and appropriate remedies
Source of background Solution
1. Highly positively charged tissue
components (eg lysine residues in histone
proteins, collagen, elastin, histamine)
attracting negatively charged gold
particles (as described in Introduction to Gold Labelling)
a) Raise the pH of the incubation buffer to reduce positive charge
b) Increase the salt content of the buffer to reduce the charge field of the gold
particles
c) Block the tissue with BSA before and during incubations
2. Non specific attraction of antibodies to
tissue components through tissue
aldehydes, fixative residues, or general
non specific binding components
a) Block the tissue with BSA before and during incubations
3. Hydrophobic tissue components (eg
tryptophan residues) attracting
hydrophobic gold particles (as described
in Introduction to Gold Labelling)
a) Add surfactant such as Tween 20 (eg 0.1-1%) to the incubation buffer
4. Sulphur containing tissue components
(eg cystein residues, epoxy resins)
attracting gold particles through dative
bonding (as described Introduction to Gold Labelling)
Add increased BSA (eg 5%) to the gold buffer only to thoroughly coat the gold with
sulphur before applying to the sections. (NB Do not add gelatin since it will
increase the attraction of gold to the section).
5. Receptors in the tissues attracting
second antibodies non specifically (eg
gold labelled Goat anti-Rabbit)
a) Block the tissue sections/membranes with
normal serum (eg 10% normal goat serum)
before primary incubation.*
b) Add normal serum (eg 1% normal goat
serum) to the incubation buffer to block the
(goat) receptor sites.*
c) Use F'ab gold conjugates (eg gold labelled
Goat (F'ab) anti-Rabbit) (see Section 3)
A typical incubating buffer, suitable for both LM and EM incubations, which provides the
components for eliminating the above sources of background may be as shown below:
Typical incubating buffer
PBS or TBS
+ 1% Normal serum* (eg goat)**
+ 0.1% Tween 20
+ 1% BSA + 0.1% sodium azide, adjusted to pH 8.2.
This buffer may be used for each step of the incubation protocol, followed by washing in
water after the final step.
NB
* Serum cannot be used in conjunction with Protein A, Protein G or Protein AG gold
conjugates since these bind IgG molecules.
** Select serum corresponding to the host of the gold labelled antibody. In this example goat
is selected because the conjugate being used is Goat anti-Rabbit.
d) Controls
In order to determine if a signal is genuine and to differentiate it from background labelling,
both positive and negative controls must be used. These are simple to perform and should
always be included in any staining protocol. Negative controls would typically include the
following:
Omit the primary antibody
Use a non specific primary antibody of the same species
Absorb the primary antibody with antigen before incubation
Use a non specific second antibody
These negative controls will help identify the source of any non specific background. A good
positive control using a specimen with high antigen content will test the whole labelling system.
Full instructions for the use of controls are given in the BBI Technical Instruction Booklet
supplied with each product.
For LM, EM and Blotting applications the correct use of silver enhancing procedures is also
important to maximise the signal and to avoid non specific background. These procedures are
described in our Silver Enhancing Section.
References
1. Hayat MA (ed) (1989-91) "Colloidal Gold. Principles. Methods and Applications". Vols
1-3, Academic press, London.*
2. Bullock GR and Petrusz P (eds) (1982-90) "Techniques in Immunocytochemistry" Vols
1, 2, 3, and 4, Academic Press, London.*
3. Baker JR (1970) "Principles of Biological Microtechnique", Methuen, London.
4. Lillie RD (1965), Histopathologic Technique and practical Histochemistry, 3rd ed,
McGraw Hill, New York.
5. Berryman MA, et al (1992) Effects of tannic acid on antigenicity and membrane contrast in
ultrastructural immunocytochemistry. J Histochem Cytochem 40, 6, 845-857
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