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Biophysical Characterization of Membrane Proteins Embedded in Nanodiscs Using Fluorescence Correlation Spectroscopy

期刊

MEMBRANES
卷 12, 期 4, 页码 -

出版社

MDPI
DOI: 10.3390/membranes12040392

关键词

fluorescent correlation spectroscopy; membrane proteins; nanodiscs; cell-free expression

资金

  1. U.S. Department of Energy by Lawrence Livermore National Laboratory [DE-AC52-07NA27344]
  2. NIH [1R01GM117342, U19AI144184]
  3. LLNL Laboratory Directed Research and Development programs [21-ERD-039, 21-ERD-047]

向作者/读者索取更多资源

Proteins embedded in biological membranes play important roles in organisms and are targets for many drugs. However, purifying these insoluble proteins has been challenging, making their detailed characterization difficult. The development of nanodisc techniques and fluorescence correlation spectroscopy (FCS) has provided new methods for studying membrane proteins. This review summarizes the current nanodisc techniques and FCS fundamentals, and discusses studies that have used FCS and nanodisc technology to investigate various membrane proteins.
Proteins embedded in biological membranes perform essential functions in all organisms, serving as receptors, transporters, channels, cell adhesion molecules, and other supporting cellular roles. These membrane proteins comprise similar to 30% of all human proteins and are the targets of similar to 60% of FDA- approved drugs, yet their extensive characterization using established biochemical and biophysical methods has continued to be elusive due to challenges associated with the purification of these insoluble proteins. In response, the development of nanodisc techniques, such as nanolipoprotein particles (NLPs) and styrene maleic acid polymers (SMALPs), allowed membrane proteins to be expressed and isolated in solution as part of lipid bilayer rafts with defined, consistent nanometer sizes and compositions, thus enabling solution-based measurements. Fluorescence correlation spectroscopy (FCS) is a relatively simple yet powerful optical microscopy-based technique that yields quantitative biophysical information, such as diffusion kinetics and concentrations, about individual or interacting species in solution. Here, we first summarize current nanodisc techniques and FCS fundamentals. We then provide a focused review of studies that employed FCS in combination with nanodisc technology to investigate a handful of membrane proteins, including bacteriorhodopsin, bacterial division protein ZipA, bacterial membrane insertases SecYEG and YidC, Yersinia pestis type III secretion protein YopB, yeast cell wall stress sensor Wsc1, epidermal growth factor receptor (EGFR), ABC transporters, and several G protein-coupled receptors (GPCRs).

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