Temperature Induced Denaturation

Temperature-induced denaturation is the loss of a protein’s native three-dimensional structure when increased thermal energy disrupts the interactions that stabilize its folded state. As temperature rises, hydrogen bonds, ionic interactions, hydrophobic packing, and other noncovalent forces become less effective, causing unfolding and often exposing normally buried regions of the polypeptide; cooling may or may not restore the original conformation. In biology, this process helps explain heat-related loss of enzyme activity, protein aggregation, and cellular stress, while laboratory denaturation supports protein characterization, food processing, sterilization, and studies of protein stability.

Temperature Induced Denaturation - Related Videos

Education

JoVE Core - Anatomy and Physiology

Protein Denaturation

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2023

The function of proteins depends on their native three-dimensional structure, which is dictated by the amino acid sequence of the specific protein. Folding of the polypeptide chain takes place under specific conditions that energetically favor the folded conformation. In contrast, protein denaturation occurs spontaneously under unfavorable conditions that disrupt the integrity of the folded conformation. Thus, the chemical and physical environment of a protein, such as significant changes in pH...

Research

JoVE Journal - Biology

Denaturing Gradient Gel Electrophoresis (DGGE)

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Cited by 10 •

2007

Denaturing Urea Polyacrylamide Gel Electrophoresis (Urea PAGE)

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Cited by 104 •

2009

Denaturing urea polyacrylamide gel electrophoresis is used to separate single-stranded DNA or RNA up to a limit of 500 nucleotides. Urea in combination with heat denatures samples and unstructured single strands migrate within the gel matrix according to their molecular weight.

Research

JoVE Journal - Biology
Free Sample

Screening for Amyloid Aggregation by Semi-Denaturing Detergent-Agarose Gel Electrophoresis

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Cited by 187 •

2008

SDD-AGE is a useful technique for the detection and characterization of amyloid-like polymers in cells. Here we demonstrate an adaptation that makes this technique amenable to large-scale applications.

Characterization of Multi-subunit Protein Complexes of Human MxA Using Non-denaturing Polyacrylamide Gel-electrophoresis

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Cited by 3 •

2016

This article describes a simple and rapid protocol to evaluate the oligomeric state of the dynamin-like GTPase MxA protein from lysates of human cells using a combination of non-denaturing PAGE with western blot analysis.

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