Posted in | News | Materials Analysis

Wyatt Publish New Application Note on DLS Protein Characterisation

Wyatt Technology Corporation, the world leader in absolute macromolecular characterization instrumentation and software, has published new application note highlighting a study made by Florida State University.

Authored by Tsz Kin Martin Tsui, Claudius Mundoma and Hong Li from Florida State University, the paper showcases how the Wyatt DynaPro dynamic light scattering (DLS) system can be used to characterize homogeneity and stability of a heterodimeric protein complex (HPC) under various buffer conditions. The results demonstrate that the pH of the buffer solutions influences the sample homogeneity and stability. To obtain a copy of the study please click here or visit the application note library available on www.wyatt.com.

A heterodimeric protein complex (HPC) from Pyrococcus furiosus is identified for its functional role in binding RNA. HPC has a total molecular weight of 65 kDa and has a tendency to form fibril materials in vitro as observed by electron microscopy. DLS data were acquired at 20°C using the Wyatt DynaPro NanoStar Dynamic Light Scattering (DLS) system. A total of 10 measurements were performed for each sample, and the stability and homogeneity determined from the polydispersity and autocorrelation functions using DLS provided information on the biophysical property of the HPC.

Hong Li, Department of Chemistry and Biochemistry and the Institute of Molecular Biophysics, Florida State University, said “Biological macromolecules are the focus of the Institute’s research – their form, function, interactions and mechanism of action. Challenging frontier areas include characterizations of the interactions between proteins and membranes, sugars or nucleic acids. The DynaPro NanoStar is ideally suited for studies of these complexes in addition to nanoparticles, vesicles, viruses and colloids. The results from the study demonstrate that the pH of the buffer solutions influences the sample homogeneity and stability, highlighting the conditions where polymerization of HPC is thermodynamically more favorable.”

The Institute of Molecular Biophysics has a long history as a unique interdisciplinary research unit dedicated to the application of physical and chemical principles to the investigation of biological phenomena. Dr. Claudius Mundoma is the Director of the Physical Biochemistry facility which houses a broad array of biophysical technology used for macromolecular characterization of structure of macromolecules. He comments, “a technique such as Dynamic Light scattering is very efficient, requiring less time and sample than other techniques to determine particle size distribution and aggregation states of molecules.” Applications include investigations to improve vitamin C production or to re-engineer viruses for the efficient delivery of gene therapies to those with inherited disorders.

Tsz Kin Martin Tsui, comments “The instrument is straightforward to operate and can be used for a broad range of applications requiring both accuracy and high sensitivity, including investigations into the folding of proteins, assembly into larger structures, stability and dynamics. The results of this study can direct me to improve sample preparation by using appropriate buffer conditions for biophysical studies, which is particularly important for structural analysis.”

The DynaPro NanoStar system from Wyatt Technology is one of the most widely used dynamic light scattering instruments for the analysis of protein solutions, promiscuous inhibitors, buffers or other products in solution. Since its inception in the early 1990's it has become an indispensable tool for biomolecular sizing and characterization. Click here for more information.

To learn more about Wyatt Technology, please visit www.wyatt.com or e-mail [email protected]

About Wyatt

With a long history of excellence in scientific instrumentation, Wyatt Technology is the recognized leader in innovative, quality light scattering instruments and software for determining the solution properties of macromolecules and nanoparticles in solution:

  • Molar mass
  • Size
  • Charge or zeta potential
  • Biomolecular interactions
  • Conformation and composition

Wyatt provides solutions for in-line multi-angle static light scattering (SEC-MALS), field-flow fractionation (FFF-MALS), composition gradients (CG-MALS), high-throughput and traditional dynamic light scattering (DLS), electrophoretic mobility (ELS), differential refractometry and differential viscosity. Through a staff comprising 20% Ph.D. scientists and many more dedicated and experienced support personnel, Wyatt's aim is to delight the customer with the best training, customer support and service available in the industry.

Citations

Please use one of the following formats to cite this article in your essay, paper or report:

  • APA

    Waters | Wyatt Technology. (2021, September 08). Wyatt Publish New Application Note on DLS Protein Characterisation. AZoM. Retrieved on April 18, 2024 from https://www.azom.com/news.aspx?newsID=37679.

  • MLA

    Waters | Wyatt Technology. "Wyatt Publish New Application Note on DLS Protein Characterisation". AZoM. 18 April 2024. <https://www.azom.com/news.aspx?newsID=37679>.

  • Chicago

    Waters | Wyatt Technology. "Wyatt Publish New Application Note on DLS Protein Characterisation". AZoM. https://www.azom.com/news.aspx?newsID=37679. (accessed April 18, 2024).

  • Harvard

    Waters | Wyatt Technology. 2021. Wyatt Publish New Application Note on DLS Protein Characterisation. AZoM, viewed 18 April 2024, https://www.azom.com/news.aspx?newsID=37679.

Tell Us What You Think

Do you have a review, update or anything you would like to add to this news story?

Leave your feedback
Your comment type
Submit

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.