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α1-Antitrypsin Polymerization: A Fluorescence Correlation Spectroscopic Study
- Source :
- Biochemistry. 44:2642-2649
- Publication Year :
- 2005
- Publisher :
- American Chemical Society (ACS), 2005.
-
Abstract
- Alpha(1)-antitrypsin (AT) is the most abundantly circulating human proteinase inhibitor in the serpin family. The polymerization of AT, leading to alpha(1)-antitrypsin deficiency, has been studied extensively in vitro by a variety of ensemble methods. Here we report the use of fluorescence correlation spectroscopy to gain further insight into this process. Measurements of the distributions of diffusion times of polymerizing AT, carried out at 45, 50, and 55 degrees C, clearly show the existence of a kinetic lag phase, during which short oligomers are formed, prior to the formation of heterogeneous mixtures of longer polymers, and suggest that long polymers, which appear to be metastable, are produced through the condensation of shorter oligomers.
- Subjects :
- Protein Denaturation
Time Factors
Polymers
Diffusion
Fluorescence correlation spectroscopy
Serpin
Photochemistry
Biochemistry
Phase (matter)
Serine
Humans
Cysteine
chemistry.chemical_classification
Microscopy, Confocal
Condensation
Temperature
Polymer
Fluorescence
Peptide Fragments
Crystallography
Spectrometry, Fluorescence
Polymerization
chemistry
alpha 1-Antitrypsin
Mutagenesis, Site-Directed
Electrophoresis, Polyacrylamide Gel
Subjects
Details
- ISSN :
- 15204995 and 00062960
- Volume :
- 44
- Database :
- OpenAIRE
- Journal :
- Biochemistry
- Accession number :
- edsair.doi.dedup.....f090e2b233d7465d85e9bca31fa5743d
- Full Text :
- https://doi.org/10.1021/bi048662e