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荧光技术已成为生物科学领域的主要工具。将GFP和DsRed等荧光蛋白与目标蛋白（POI）融合，能够实现表达分析和体内蛋白定位。然而，由于这些融合蛋白的分子量较大，其应用受到了限制。此外，相关的分子生物学操作繁琐且耗时。与目标蛋白（POI）共价结合的小型荧光团可能有助于解决这一问题。对半胱氨酸的巯基进行荧光标记是研究目标蛋白（POI）的结构、功能及相互作用时的首选方法。（请注意：我们公司提供一种即用型试剂盒，可用于用高质量小型荧光团标记半胱氨酸残基（产品型号：FP202），适用于蛋白质活性及功能研究。）然而，最常见的蛋白质标记方法是胺修饰。像NHS酯这类胺反应性荧光团很容易与存在于N端[1]以及赖氨酸侧链中的伯氨基发生反应，形成稳定的共价键。这款蛋白质标记试剂盒旨在用小型荧光团标记目标蛋白（POI）的赖氨酸，从而生成荧光蛋白-荧光团偶联物。该试剂盒包含进行10次独立标记反应所需的所有试剂，每次反应可处理1毫克目标蛋白（POI）。
For general laboratory use.
Shipping: shipped on gel packs
Storage Conditions: store at -20 °C
store dark, see manualShelf Life: 12 months
Spectroscopic Properties:
Excitation maximum: λexc = 649 nm Emission maximum: λem = 670 nm Extinction coefficient: εmax = 250,000 mol-1 cm-1 Correction factor: CF280 nm = 0.05Content:
Cy5 NHS-ester
1 vial containing 1 mgDimethylformamide (DMF)
200 μlSodium bicarbonate
1 vial containing 84 mgultra-pure water
1 mlStorage and Stability:
Upon receipt store the dye at -20 °C. The other components may be stored at room temperature. If stored as recommended, Jena Bioscience guarantees optimal performance of this product for 12 months.Protocol:
General notes
The optimal protein concentration is 10 mg/ml, other concentrations are also possible, however, it should be at least 2 mg/ml since labeling efficiency suffers from lower protein concentrations. We recommend using about 1 mg protein per labeling reaction.
Buffers containing primary amines such as Tris and glycine are not suitable for the labeling reaction and must be exchanged with suitable amine-free buffer such as PBS, MES, or HEPES before starting the labeling reation.Experimental protocol
- Dissolve the sodium bicarbonate by adding 1 ml ultra-pure water. The resulting 1 M solution is stable at 4 °C for at least 2 weeks.
- Add the appropriate volume of sodium bicarbonate (1 M) to your protein solution to achieve a final concentration of 100 mM.
- Prepare the dye by adding 100 μl DMF resulting in a dye concentration of 10 mg/ml. Vortex until the NHS ester is completely dissolved! We recommend preparing the solution shortly prior to use however, it is stable for two weeks at -20 °C. Whenever handling the fluorophore or conjugate, work under low light conditions!
- Add 100 μl protein solution (10 mg/ml) and 10 μl dye (10 mg/ml) to an appropriate vial. Vortex carefully and centrifuge briefly to collect the reaction mixture at the bottom of the tube.
- Incubate for one hour in a shaker at room temperature. Protect from light!
- Purify the conjugate using standard gel filtration columns such as Sephadex G-25 or similar. Alternatively, the free dye may be separated from the conjugate by dialysis or appropriate spin concentrators.
Please note that protein purification materials are not provided with the kit!
Concentration of the conjugate
Since there may occur a certain loss of protein during labeling and particularly during purification measuring the concentration of the conjugate is important for further application. The concentration of a protein is commonly determined by measuring its absorbance at 280 nm. As shown in the excitation spectrum of Cy5 however, the fluorescent dye absorbs at 280 nm as well thereby increasing the ε280 for the conjugate. Therefore, a correction factor (CF) is required to eliminate the contribution of the dye at 280 nm.
The CF of each dye is given in the Spectroscopic Data section, and hence the concentration of the conjugate is calculated according to:c (mg/ml) = ((A280 - Amax x CF) / ε280 ) x MWprotein
A280 absorbance of the conjugate solution measured at 280 nm Amax absorbance of the conjugate solution measured at λexc λexc, εmax, CF intrinsic properties of the Atto dye, please refer to Spectroscopic Prop ε280, MW intrinsic properties of your protein, if not known they can be obtained from web sources such as ExPASy Proteomics Server[2] Degree of labeling (DOL)
The DOL specifies the average number of fluorophore molecules per molecule of conjugate. It is an important parameter of the conjugate significantly affecting further applications. For most purposes, a DOL of approximately 1 molecule of fluorophore per 200 amino acids is ideal, also see section Troubleshooting.
The DOL is calculated according to:DOL = (Amax x ε280) / ((A280 - Amax x CF) x εmax)
Example for determining the conjugate concentration and the DOL of BSA (Bovine serum albumin), labeled with Atto 488 NHS ester:
BSA: ε280 = 42,925 M-1 cm-1, MW = 66,433 Da
Atto 488: λexc = 501 nm, εmax = 90,000 M-1 cm-1, CF = 0.1After labeling and purification the absorption of the conjugate solution is measured at 280 and 501 nm, respectively.
- absorption A280 1.69 A501 7.23
The conjugate concentration and the DOL are calculated:c (mg/ml) = ((A280 - Amax x CF) / ε280 ) x MWprotein
c (mg/ml) = ((1.69 - 7.23 x 0.1) /42,925 ) x 66,433
c (mg/ml) = 1.5DOL = (Amax x ε280) / ((A280 - Amax x CF) x εmax)
DOL = (7.23 x 42,925) / ((1.69 - 7.23 x 0.1) x 90,000)
DOL = 3.57In this experiment the concentration of the conjugate is 1.5 mg/ml and most protein molecules are labeled with three or four Atto 488 molecules corresponding to 1.2 molecules of Atto 488 per 200 amino acids.
Please note that the spectroscopic determination of the concentration and the DOL of the conjugate is not absolutely correct. The spectroscopic characteristics of the free dye are not exactly the same as of the dye bound to the POI. Also, the spectroscopic characteristics of the native protein at 280 nm differ from those of the conjugate.
In general, these changes are negligibly small and therefore, spectroscopic determination of the concentration and the DOL of the conjugate is the most frequently used method[3] .
In addition to the spectroscopic measurements, one may analyze the conjugate by SDS-PAGE and subsequent fluorescence scanning of the gel. Only one band (consisting of the fluorescently labeled protein) should be visible in the fluorescent scan. If there is an additional band at very low molecular weight, the conjugate solution still contains free dye and must be purified again.Storage of the Conjugate
Protect from light! Store the conjugate just like the unlabeled protein. We recommend dividing the solution into small aliquots and freeze at -20 °C or -80 °C. Avoid repeated freezing and thawing!Troubleshooting:
Inefficient Labeling- Concentration of protein solution
The assay is optimized for labeling of 1 mg protein at a concentration of 10 mg/ml.
Increase the amount of dye proportionally for protein concentrations above 10 mg/ml. If your protein concentration is very low (< 1 mg/ml) apply spin concentrators to achieve a final concentration of 2 mg/ml.
The efficiency of labeling is strongly concentration dependent and varies among different proteins. Thus, in every single case optimization might be necessary to obtain the desired degree of labeling. - Buffer composition
Protein solutions containing primary amines (even traces thereof) dramatically decrease labeling efficiency. Make sure that your protein is extensively dialyzed in case it has been in contact with amine-containing substances. - Impact of the pH
Check the pH of your protein solution! The reference range is 8.2 - 8.5.
The primary amino groups of the protein must not be protonated to be reactive thus, the pH of the protein solution has to be sufficiently high. On the other hand, the hydrolysis rate of NHS esters increases with the pH of the solution, resulting in non-reactive dye. Optimal labeling results have been obtained at pH 8.3.
100 mM sodium bicarbonate might not be sufficient to raise the pH to optimum in strongly buffered protein solutions at a lower pH. You may add more sodium bicarbonate until the optimal pH is achieved.
Note that labeling efficiency not only depends on the surrounding conditions but also on the protein characteristics. The tertiary structure and the resulting number of lysines on the surface of the protein play a role as well as the isoelectrical point and the behaviour of the protein at pH 8.3.Overlabeling
Reasons for overlabeling can be a high number of lysines on the surface of your protein and/or optimal characteristics of the protein at pH 8.3.
To prevent overlabeling, decrease the amount of dye or increase the protein concentration. You may also reduce the reaction time.Purification of the conjugate
The dye is unstable in aqueous solutions - the hydrolysis rate of NHS esters increases with the pH of the solution. Thus, a certain amount of free dye is produced in each labeling reaction and needs to be separated from the conjugate.
If your purified conjugate still contains traces of free dye apply it to a second purification step. Check the purity of your conjugate by SDS-PAGE.
Separation of free dye from the conjugate becomes more difficult at higher concentrations of free dye. The column or membrane might even be blocked by the dye at very high concentrations, so try to optimize the labeling reaction in order to decrease the concentration of free dye. Keep in mind that overall yield suffers from additional purification steps.What DOL is optimal?
As a basic rule one dye per 200 amino acids is ideal however, the optimal degree of labeling depends on your protein as well as on your intended application. If you are not sure, check your assay with small amounts of conjugate at different DOLs to obtain optimal results.
In any case prevent overlabeling since this may cause protein aggregation or fluorescence quenching of neighbouring dyes. -
产品组分
内容 型号
规格 储存温度
Cy5蛋白标记试剂盒
CNFP201CY5-01 10次
-20°C Cy5蛋白标记试剂盒
CNFP201CY5-02 20次
-20°C 操作手册
1 1 常温
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注意事项
保存建议 厂家推荐蓝冰运输。当您收到产品后，按照说明书建议保存于-20°C。 -
FAQ
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Selected References:
[1] The α-amino group at the protein's N-terminus may be labeled selectively by performing the labeling reaction at pH 7.0
[2] www.expasy.ch/tools/protparam.html
[3] Brinkley (1992) A Brief Survey of Methods for Preparing Protein Conjugates with Dyes, Haptens, and Cross-Linking Reagents. Bioconjugate Chem. 3:2.Cryo-EM and cryo-ET reveal the molecular architecture and host interactions of mycobacteriophage Douge.
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ACS Omega | 2018 Jun 28 | 30221235
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