CD Formulation specializes in offering our clients accurate analysis of nucleic acid secondary structures. Using cutting-edge methods like circular dichroism, we precisely assess how nucleic acids absorb circularly polarized light to glean detailed structural insights.
In biotechnology, scrutinizing nucleic acid drugs' secondary structures is vital as they affect physical/chemical properties and biological roles. DNA's helix ensures accurate gene replication and transfer, while the diverse forms of RNA enable it to modulate genetic activity and facilitate protein creation. Understanding these structures aids researchers in deciphering their functional mechanisms, refining sequence designs, and predicting molecular interactions, thus underpinning the development of nucleic acid drugs with essential scientific insights.
Items | Descriptions |
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Sequence or Structure Conservation Analysis | By comparing the sequence and structural conservation among different nucleic acid molecules, tools are used for alignment followed by structure prediction and sequence matching to identify conserved structural features of nucleic acid drugs. |
Experiment-Driven Data Analysis | Using high-throughput experimental techniques such as deep sequencing, we acquire vast nucleic acid sequence data. Bioinformatics methods are then employed for data processing and feature description, enabling more accurate detection of novel structural features in nucleic acid drugs. |
Thermodynamic analysis is critical in secondary structure research of nucleic acid drugs. By simulating various physiological and experimental conditions, we can accurately assess the thermodynamic stability of structures. This includes evaluating the melting temperature and melting curves of secondary structures at different temperatures and salt concentrations to reveal the thermal stability of nucleic acid molecules. Additionally, using high-performance computational technology for detailed polymorphism analysis can predict the conformational distribution, transition barriers, and conversion rates of nucleic acids in various biological environments.
Our conformational simulation services offer an advanced and comprehensive toolkit focused on the detailed modeling and analysis of molecular and material conformations. We incorporate the latest techniques in quantum mechanical calculations, molecular dynamics, and machine learning, ensuring precise predictions of molecular behavior across different scales. Our platform supports highly customizable simulation processes, allowing users to define conditions and parameters to meet specific research needs.
Fig.1 Flow chart of nucleic acid purity secondary structure analysis. (CD Formulation)
Platforms | Descriptions |
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CD Platform | Using circular dichroism, we gather insights into nucleic acids' secondary structures by observing their differential absorption of circularly polarized light, allowing us to pinpoint the arrangement and ratio of double and single strands. |
UV Spectroscopy Platform | This method examines nucleic acids' melting curves, offering insights into secondary structure stability. It assesses absorbance changes across temperatures to identify the transition temperature, revealing thermal stability. |
HPLC Platform | Essential for analyzing and purifying nucleic acid samples, HPLC separates nucleic acids by molecular weight or structure, yielding high-purity samples for analysis. It ensures quality by assessing polymer purity and binding states. |
MS Platform | Mass spectrometry accurately detects the mass information of nucleic acids, aiding in the identification of any chemical modifications or degradation products. Combined with other techniques, MS provides critical data for structure confirmation and molecular composition, supporting more comprehensive structural characterization. |
Technology: Nucleic acid secondary structure analysis by CD technology
Journal: Structural genomics: general applications
IF: 6.6
Published: 2021
Results:
Beyond its standard double helix form, DNA can adopt various secondary structures through inter- and intramolecular hydrogen bonds. These structures go through multiple, complex, and interchangeable conformations, with transient intermediates that conventional ensemble methods find hard to detect. However, single-molecule FRET (sm-FRET) microspectroscopy effectively addresses this by observing biological processes at rapid rates, allowing real-time tracking of molecular transitions. This technique directly measures rate constants for each transition, including those of fleeting intermediates not easily detected in bulk populations.
Fig.2 Schematic representation of the secondary structure components. (Micsonai A, et al., 2021)
For more details about our nucleic acid secondary structure analysis services or any related collaboration inquiries, please feel free to contact our team. Our expert team will provide you with professional support and guidance to assist you in your research and development journey.
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