4.7 Article

Novel gene-encoded intermolecular FRET sensor for tracking glycosylation of CD147 in living cells

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 413, Issue 12, Pages 3193-3199

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-021-03256-0

Keywords

CD147; Glycosylation; FRET sensors

Funding

  1. Major Research Plan of the National Natural Science Foundation of China [2016YFA0101200]
  2. National Natural Science Foundation of China [21778050, 91749125]
  3. Youth Fund of National Natural Science Foundation of China [81701232]
  4. New Medical Science Joint Fund of USTC [WK2070000123]
  5. Training Program of the Major Foundation of USTC [WK3520000007]

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A gene-encoded FRET sensor was developed for detecting CD147 glycosylation in live cells, allowing continuous monitoring of the deglycosylation process and providing a new strategy for analyzing other glycosylated proteins.
CD147 is involved in various physiological processes and plays important roles for tumor metastasis. Glycosylation of the protein determines numerous functions of CD147. Up to now, hardly any sensor has been developed for detecting glycosylation of CD147 in live cells. There is a pressing requirement of development of a selective and continuous biosensor for cell imaging. The emergence of gene-encoded fluorescence resonance energy transfer (FRET) sensor provides a new way to develop the sensors to analysts. We designed and constructed novel gene-encoded FRET proteins sensing glycosylation of CD147 by measuring FRET ratio of two intermolecular motifs. With the decrease of CD147 glycosylation level in cells, the FRET ratio increased significantly. The specificity of the sensor targeting to CD147 was also determined by siRNA interference experiment. Finally, continuous living cell image of deglycosylation process of CD147 using the newly developed sensor has been performed successfully. The work not only provides useful tools for analyzing glycosylation of CD147 in living cells, but also implicates alternative strategy for detecting other glycosylated proteins.

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