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  6. 5'-TFA-Amino Modifier 11 CE-Phosphoramidite

5'-TFA-Amino Modifier 11 CE-Phosphoramidite

5'-TFA-Amino Modifier 11 CE-Phosphoramidite

5'-TFA-Amino Modifier 11 CE-Phosphoramidite

Phosphoramidite for the incorporation of an amino function at the 5' end of an oligonucleotide for solution-phase conjugation.

Key features

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  • Incorporates primary amine to 5' end of an oligonucleotide, for subsequent conjugation.
  • Espcecially suited to solution-phase conjugation due to "built-in" hydrophilicity of TEG spacer.
  • Base-labile trifluoacetyl (TFA) protection useful where purification of oligo is not necessary.
  • Once incorporated into an oligo this linker is equivalent to ~2 base units.
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Product information

Incorporation of a primary amine reactive functional group at specific sites within an oligonucleotide allows for subsequent post-synthesis conjugation of the oligo with a number of different affinity, reporter or protein labels, depending on the application. Such labels need to be reactive towards the incorporated functional group: for example, NHS esters or isothiocyanates will react with primary amines. This approach is often necessary where the desired label or tag is either not available as a phosphoramidite, or is sensitive or unstable to the conditions of oligonucleotide synthesis or deprotection. A common example is the attachment of a rhodamine dye using the TAMRA NHS ester. Functionally-derivatised oligos can also be covalently attached to surfaces such as glass slides or gold microspheres for use in various microarray or nanoelectronic applications.

Our hydrophilic “amino-modifier 11” products (incorporating a triethylene glycol spacer) are particularly useful for solution-phase couplings of labels to oligos. It is often found that when using hydrophobic amino-linkers, e.g. LK2123/BNS-5015, an additional hydrophilic spacer is required. This extends the distance of the label from the oligo. The amino-11 products has this hydrophilicity “built-in” and can therefore be used where a hydrophilic linker is required.

Once incorporated into an oligo this linker is equivalent to ~2 base units. It is available in both TFA and MMT protected forms, the latter allowing oligo purification based on exploiting the trityl group, or on-column conjugations.

Applicable Products

LK2123 5'-MMT-Amino-Modifier-C6-CE Phosphoramidite
LK2124 5'-TFA-Amino-Modifier-C6-CE Phosphoramidite
LK2133 5'-MMT-Amino-Modifier-C12-CE Phosphoramidite
LK2182 5'-TFA-Amino-Modifier 11 CE Phosphoramidite
LK2193 5'-MMT-Amino-Modifier 11 CE Phosphoramidite
LK2532 5'-TFA-Amino-Modifier-C12-CE Phosphoramidite
LK2534 5'-TFA-Amino-Modifier-C5-CE Phosphoramidite

Physical & Dilution Data

Dilution volumes (in ml) are for 0.1M solutions in dry acetonitrile (LK4050). Adjust accordingly for other concentrations. For µmol pack sizes, products should be diluted as 100µmol/ml to achieve 0.1M, regardless of molecular weight.

Item

Mol. Formula

Mol. Wt.

Unit Wt.

250mg

500mg

1g
LK2123 C35H48N3O3P 589.76 179.16 4.24 8.48 16.96
LK2124 C17H31N3O3PF3 413.42 179.16 6.05 12.09 24.19
LK2133 C41H60N3O3P 673.92 263.32 3.71 7.42 14.84
LK2182 C19H35F3N3O6P 489.47 255.21 5.11 10.22 20.43
LK2193 C37H52N3O6P 665.81 255.21 3.75 7.51 15.02
LK2532 C23H43N3O3PF3 497.58 263.32 5.02 10.05 20.10
LK2534 C16H29N3O3PF3 399.39 165.06 6.26 12.52 25.04

Dissolution

For all, prepare the amidite solution 5-10min before placing on the synthesiser to ensure complete dissolution.

Coupling

A 5min coupling time is recommended.

LK2193 - A 2min (120s) coupling time is recommended.

Deblocking

For TFA-protected 5’-amino modifiers (LK2124, LK2182, LK2532 and LK2534) this final step is not required. For MMTr 5’-modifiers (LK2123, LK2133 and LK2193) it is better to retain the MMTr protection and remove this during or after purification.

Cleavage, Deprotection & Purification

For all amino modifiers it is recommended that the synthesis column is washed with 10-20% DEA/acetonitrile for 3min prior to cleavage from the support. This will remove the cyanoethyl groups that can react with the free amino or thio groups during deprotection, blocking these site with acrylonitrile. The resin must then be thoroughly washed (acetonitrile) and dried (Ar, He, N2, air) prior to cleavage and base deprotection.

If fast deprotection on standard amidites (G, C) is used, e.g. Ac-dC and/or dmf-dG, cleavage and deprotection can be carried out in either AMA (35min at 65˚C or 2h at RT) or ammonium hydroxide solution (2h at 55˚C). If Bz-dC and iBu-dG are used then cleavage and deprotection is done using ammonium hydroxide solution (2.5h at 70˚C, 4h at 55˚C, or overnight at 55˚C).

For TFA-protected modifiers the TFA group is lost during deprotection. If the intended use is post-synthesis labelling the oligo with an active ester (e.g. TAMRA, LK0251), it is recommended that the oligo is desalted prior to the labelling reaction.

MMTr protection is stable to base treatment and this can be used to aid purification in e.g. “DMT ON” HPLC or cartridge purification. If, after purification or desalting, the MMTr group still needs to be removed this is typically carried out using 80% acetic acid/water for 30min and the oligo is immediately desalted.

Determination of coupling efficiency for MMTr Modifiers

This procedure is used solely for the purpose of determining coupling efficiency; it should not be used for routine deprotection. The calculation is based on a comparison of the absorbance of the MMTr cation at 472nm versus the absorbance of the DMTr cation at 497nm. The ratio factor (RF) of the absorbance of a standard solution is:

RF = A-DMTr(497)/A-MMTr(472) = 1.33
  1. Carry out the synthesis (1μmol) in the DMT ON mode.
  2. Collect the last DMTr solution in a 100ml volumetric flask and make up to the mark with 0.1M toluenesulphonic acid in anhydrous acetonitrile (TSA). Zero the instrument with TSA at 497nm and then measure the absorbance (A1) at 497nm.
  3. After the synthesis is complete, remove the synthesis column and manually deblock the MMTr group with aliquots of the normal deblocking mix until all the yellow colour has eluted. This process takes up to 15min. Collect the solution in a 100ml volumetric flask and make to 100ml with TSA. Measure the absorbance (A2) at 472nm.
  4. Calculate the coupling efficiency using the formula:
Coupling (%) = A2/A1 x 1.33 x 100

Note that, due to incomplete deblocking of the MMTr group, this procedure yields a coupling efficiency determination about 5% below the actual coupling efficiency.

The modified oligonucleotide may be purified using a cartridge, HPLC, or gel electrophoresis. Cartridge purification is accomplished using the DMT ON procedure. MMTr removal on the cartridge is not reliable with a standard 2% aqueous trifluoroacetic acid (TFA) wash, therefore 2 additional TFA washes are required.

Alternatively, treatment of the purified DMT ON oligo (see below) with acetic acid:water (80:20) in solution at room temperature for 1h will remove the MMTr group. Precipitate the oligo with an ethanol/2.5M sodium acetate precipitation. Again, complete removal is not achieved therefore additional HPLC is required.

RP-HPLC may be performed either before or after attachment of the label. If purification is desired prior to a label attachment, the MMTr group should not be removed from the oligo as the lipophilic nature of the group aids in HPLC purification. RP-HPLC is best carried out using a C18 or equivalent column. The MMTr group can be removed in cartridge purification or by treatment with acetic acid in solution as above.

Storage & Stability

The oils are stored dry in a freezer at –10 to –30°C. Acetonitrile solutions must be used within 24h.

SDS

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