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Probing Membrane Protein Association Using Concentration-Dependent Number and Brightness.


ABSTRACT: We introduce concentration-dependent number and brightness (cdN&B), a fluorescence fluctuation technique that can be implemented on a standard confocal microscope and can report on the thermodynamics of membrane protein association in the native plasma membrane. It uses transient transfection to enable measurements of oligomer size as a function of receptor concentration over a broad range, yielding the association constant. We discuss artifacts in cdN&B that are concentration-dependent and can distort the oligomerization curves, and we outline procedures that can correct for them. Using cdN&B, we characterize the association of neuropilin 1 (NRP1), a protein that plays a critical role in the development of the embryonic cardiovascular and nervous systems. We show that NRP1 associates into a tetramer in a concentration-dependent manner, and we quantify the strength of the association. This work demonstrates the utility of cdN&B as a powerful tool in biophysical chemistry.

SUBMITTER: Paul MD 

PROVIDER: S-EPMC7940563 | biostudies-literature | 2021 Mar

REPOSITORIES: biostudies-literature

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Probing Membrane Protein Association Using Concentration-Dependent Number and Brightness.

Paul Michael D MD   Rainwater Randall R   Rainwater Randall R   Zuo Yi Y   Gu Luo L   Hristova Kalina K  

Angewandte Chemie (International ed. in English) 20210204 12


We introduce concentration-dependent number and brightness (cdN&B), a fluorescence fluctuation technique that can be implemented on a standard confocal microscope and can report on the thermodynamics of membrane protein association in the native plasma membrane. It uses transient transfection to enable measurements of oligomer size as a function of receptor concentration over a broad range, yielding the association constant. We discuss artifacts in cdN&B that are concentration-dependent and can  ...[more]

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