Sensitive Detection of Protein Binding to the Plasma Membrane with Dual-Color Z-Scan Fluorescence

Isaac Angert, Siddarth Reddy Karuka, Jared Hennen, Yan Chen, Joseph P. Albanesi, Louis M. Mansky, Joachim D. Mueller

Research output: Contribution to journalArticlepeer-review

Abstract

Delicate and transitory protein engagement at the plasma membrane (PM) is crucial to a broad range of cellular functions, including cell motility, signal transduction, and virus replication. Here, we describe a dual-color (DC) extension of the fluorescence z-scan technique, which has proven successful for quantification of peripheral membrane protein binding to the PM in living cells. We demonstrate that the coexpression of a second, distinctly colored fluorescent protein provides a soluble reference species that delineates the extent of the cell cytoplasm and lowers the detection threshold of z-scan PM-binding measurements by an order of magnitude. DC z-scan generates an intensity profile for each detection channel that contains information on the axial distribution of the peripheral membrane and reference protein. Fit models for DC z-scan are developed and verified using simple model systems. Next, we apply the quantitative DC z-scan technique to investigate the binding of two peripheral membrane protein systems for which previous z-scan studies failed to detect binding: human immunodeficiency virus type 1 (HIV-1) matrix (MA) protein and lipidation-deficient mutants of the fibroblast growth factor receptor substrate 2α. Our findings show that these mutations severely disrupt PM association of fibroblast growth factor receptor substrate 2α but do not eliminate it. We further detected binding of HIV-1 MA to the PM using DC z-scan. Interestingly, our data indicate that HIV-1 MA binds cooperatively to the PM with a dissociation coefficient of Kd ∼16 μM and Hill coefficient of n ∼2.

Original languageEnglish (US)
Pages (from-to)281-293
Number of pages13
JournalBiophysical journal
Volume118
Issue number2
DOIs
StatePublished - Jan 21 2020

Bibliographical note

Funding Information:
This work was supported by the National Institutes of Health , grants GM064589 (J.D.M., J.H., S.R.K., and Y.C.), GM121536 (J.P.A., Y.C., and J.D.M.), and GM124279 (L.M.M., I.A., and J.D.M.). I.A. was supported by National Institutes of Health grant T32 AI083196 .

Publisher Copyright:
© 2019 Biophysical Society

PubMed: MeSH publication types

  • Journal Article
  • Research Support, N.I.H., Extramural

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