Aptamers are nucleic acid sequences or single-stranded oligonucleotides with specific sequences that fold and bind selectively to particular molecules or targets. CD Formulation, a leading biotechnology company, provides a comprehensive range of services to develop high-quality, customized aptamers for research, diagnostic, and therapeutic applications.
Aptamers are short sequences of nucleotides, usually ranging from 20 to 100 units of DNA/RNA. They have a unique three-dimensional shape that allows them to specifically recognize and bind to target molecules with high affinity. These molecules are synthetically produced in a laboratory through chemical processes, which provides benefits like quick production times, low costs, high stability, and a great degree of specificity.
The small and flexible structure of aptamers enables them to bind to smaller targets or concealed domains that antibodies cannot access. Additionally, aptamers can serve as carriers for drug delivery, such as in aptamer-drug conjugates (ApDCs), allowing for the precise delivery of drugs, including chemotherapeutic agents, therapeutic RNAs, toxins, and radioisotopes, directly into cancer cells.
Fig.1 Features of Aptamer. (CD Formulation)
CD Formulation has extensive experience in the synthesis of small nucleic acids and offers nucleic acid aptamer synthesis services based on protein targets.
SELEX is a well-established and widely used technique for selecting high-affinity aptamers. SELEX consists of incubation, combination, distribution, and amplification, which are repeated four times.
First, a library of random oligonucleotide sequences (the starting library) is incubated with target molecules. During this incubation, some sequences bind to the target molecules, while others bind weakly or do not interact with them at all. The bound sequences are then separated from the weakly bound or unbound sequences.
Next, the eluted oligonucleotides are amplified using polymerase chain reaction (PCR) for DNA sequences and reverse transcription PCR (RT-PCR) for RNA sequences to enrich the library.
Then, the obtained single-stranded DNA was then utilized for the subsequent round of selection. The processes of binding, isolation, and amplification must be repeated to achieve a sufficiently enriched nucleic acid pool of target-binding sequences. Typically, an enriched nucleic acid pool can be obtained through 5 to 15 rounds. The enriched pool is sequenced, and candidate aptamers are identified from the sequencing results using bioinformatics analysis.
Finally, the selected aptamers are chemically synthesized and characterized.
Fig.2 Flow chart of aptamer preparation. (CD Formulation)
Design the initial nucleic acid sequence of the aptamer using bioinformatics tools to enhance its binding affinity for the target molecule.
Synthesize diverse libraries containing a wide variety of nucleic acid sequences to identify the most suitable aptamer in the subsequent screening steps.
The selection of aptamers with high affinity and specificity for the target is achieved through a systematic evolutionary enrichment and screening technique (SELEEX) applied to nucleic acid libraries.
The screened aptamer sequences are further optimized to enhance their stability and binding efficiency.
Synthesize the optimized aptamer and chemically modify it to enhance its functionality or stability based on the specific application requirements.
In vitro and in vivo experiments are conducted to verify the binding properties and biological activities of the synthesized aptamers, ensuring their effectiveness.
Successful aptamer design typically involves multiple cycles of screening and amplification to progressively enhance the affinity and specificity of the aptamer sequence.
When a particular aptamer sequence is ready, the following phase involves its preparation using either chemical synthesis or enzymatic in vitro transcription. Chemical synthesis is usually used for creating smaller nucleic acid fragments, whereas in vitro transcription is better suited for longer sequences.
CD Formulation's analytical techniques can be employed to assess the purity and accuracy of nucleic acids, thereby confirming their effectiveness in practical applications.
Technology: Aptamers are chosen using Systematic Evolution of Ligands by Exponential Enrichment (SELEX) technology
Journal: Molecules
IF: 2.791
Published: 2024
Results:
Aptamers frequently surpass conventional antibodies due to their unique properties, including small size, ease of synthesis and modification, low cost, and low immunogenicity. This has led to ongoing interest in their engineering for applications in diagnostics and therapeutics. Recently, aptamers have shown promise as early diagnostic biomarkers and for precision medicine in neurodegenerative and neurological diseases. Here, the authors provide insights into neurotargeting aptamers and their potential applications in neuroscience research, neurodiagnostics and neurology.
Fig.3 Chemical modifications of DNA or RNA building blocks for aptamers. (Wang B, et al., 2024)
CD Formulation offers custom synthesis services for aptamers, encompassing the entire process from target selection and sequence design to synthesis and optimization. Through meticulous screening and optimization, we ensure that the aptamers exhibit high specificity and affinity to meet our customers' research and application requirements. Contact us for professional aptamer customization solutions tailored to your needs.
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