Creative
Biostructure, a biotechnology company specialized in providing products and
services in structural science, offers various thermodynamics analytical
services to study the binding mechanism of biomolecules. Recently, Creative
Biostructure enhanced its thermal
gravimetric analysis services covering food, pharmaceuticals, polymers, as
well as other materials.
Thermal
Gravimetric Analysis (TG or TGA)
refers to a thermal analysis technique that measures the relationship between
the mass of the sample to be tested and the temperature change under
program-controlled temperature, and is used to study the thermal stability and
composition of materials. It is worth mentioning that the definition of mass
change rather than weight change is based on the fact that under the action of
a magnetic field, when ferromagnetic materials reach the Curie point, although
there is no mass change, there is apparent weightlessness.
TGA
is a commonly used detection method in research and development and quality
control. Thermogravimetric analysis is often used in combination with other
analysis methods in actual material analysis to conduct comprehensive thermal
analysis and analyze materials comprehensively and accurately.
Typical applications of TGA at Creative Biostructure
include:
*Determining
thermal stability—if a substance (such as ceramic or polymer) is thermally
stable, no mass change will be seen.
*The
most prevalent visible losses in TGA are oxidative mass losses, which are used
to determine oxidative stability. As a result, it is critical to investigate
the oxidation resistance of copper alloys.
*Compositional
analysis-temperature and weight change of decomposition reactions can allow
quantitative composition analysis.
*Determination
of the purity of a mineral, inorganic compound, or organic material.
*Measurement
of the weight of fiberglass and inorganic fill materials in laminates,
plastics, paints and composite materials.
*Determination
of water/ carbon content or other residual solvents in a material.
*Analysis
of reactions with air, oxygen, or other reactive gases.
*Enhancement
of product formulation processes
TGA
equipment from Creative Biostructure can be used to ramp temperature from room
temperature to 1000°C in various gas atmospheres such as nitrogen, air, or
other inert gases. Furthermore, sample weight can range from 1 mg to 150 mg,
with a sensitivity of 0.01 mg for weight change.
Protein
Thermal Shift Assay, Surface Plasmon Resonance, Isothermal Titration Calorimetry,
Differential Scanning Calorimetry, Saturation-Transfer Difference and Bio-Layer
Interferometry (BLI)
Technology are those analytical methods for biophysical characterization of
biomolecules available at Creative Biostructure.
To know more detailed information about the thermal gravimetric analysis service provided by Creative Biostructure, please visit https://www.creative-biostructure.com/maghelix%E2%84%A2-thermal-gravimetric-analysis-tga-216.htm
Gene
editing is one of the latest breakthroughs in biology. The well-known
CRISPR-Cas gene editing system confers immunity against foreign DNA to
prokaryotes (organisms lacking a cell nucleus). Since the discovery of CRISPR
gene editing technology, scientists have revealed how CRISPR-cas proteins
evolved from their precursors. This knowledge will help them develop other
small new genome editing tools for gene therapy.
At
the University of Tokyo, Professor Osamu Nureki's team worked to identify the
structure and function of proteins involved in genome editing. In a recent
study by the team, they discovered the 3D structure of
proteinTnpB, a possible precursor to the CRISPR-Cas12
enzyme. Their findings were published in Nature.
Previous
research has shown that the TnpB protein may act like a pair of molecular
scissors, cutting DNA with the help of a special type of non-coding RNA called
omega RNA. But how RNA-guided DNA cleavage works, and its evolutionary
relationship to the Cas12 enzyme, was unclear, prompting research from Nureki's
lab. The first and most critical step in their understanding was to reveal the
protein's structure.
To
determine the three-dimensional structure of TnpB, the researchers extracted
the TnpB protein from a bacterium called Deinococcus radiodurans and used
cryo-electron microscopy. In cryo-electron
microscopy, a protein sample is cooled to -196°C
using liquid nitrogen and illuminated with an electron beam, revealing the
protein's 3D structure.
The
team found that the omega RNA in TnpB has a unique pseudoknot shape, similar to
the guide RNA for the Cas12 enzyme. The study also revealed how TnpB recognizes
omega RNAs and cleaves target DNA. When they compared the structure of this
protein to the Cas12 enzyme, they learned two possible ways that TnpB might
have evolved into a CRISPR-Cas12 enzyme.
"Our
findings provide mechanistic insights into TnpB function and advance our
understanding of the evolution of TnpB proteins to CRISPR-Cas12 effectors,”
said Ryoya Nakagawa, one of the first authors of the research paper. He added
that, “In the future, we will explore the potential application of tnpb-based
gene editing technology.”
About the author
Collected
by Creative Biostructure. Creative Biostructure has been working in the field
of structural biology, membrane protein technologies, and structure-based drug
discovery. We have expertise and experience in protein 3D structure prediction,
protein modeling, and data analysis. Related services include: Rheo-NMR
service, co-crystallization,
membrane protein structure determination by solid-state NMR, stable isotope
labeling for nucleic acids, crystallization chaperone strategies, and
immunoelectron microscopy service.