Literature DB >> 30239200

Comprehensive Study of the Self-Assembly of Phospholipid Nanodiscs: What Determines Their Shape and Stoichiometry?

Nicholas Skar-Gislinge1, Nicolai Tidemand Johansen1, Rasmus Høiberg-Nielsen1, Lise Arleth1.   

Abstract

Phospholipid nanodiscs have quickly become a widely used platform for studies of membrane proteins. However, the molecular self-assembly process that ultimately should place a membrane protein inside a nanodisc is not well understood. This poses a challenge for a successful high-yield reconstitution of general membrane proteins into nanodiscs. In the present work, the self-assembly process of POPC-MSP1D1 nanodiscs was carefully investigated by systematically modulating the reconstitution parameters and probing the effect with a small-angle X-ray scattering analysis of the resulting nanodiscs. First, it was established that nanodiscs prepared using the standard protocol followed a narrow but significant size distribution and that the formed nanodiscs were stable at room temperature over a time range of about a week. Systematic variation of the POPC/MSP1D1 stoichiometry of the reconstitution mixture showed that a ratio of less than 75:1 resulted in lipid-poor nanodiscs, whereas ratios of 75:1 and larger resulted in nanodiscs with constant POPC/MSP1D1 ratios of 60:1. A central step in the self-assembly process consists in adding detergent-absorbing resin beads to the reconstitution mixture to remove the reconstitution detergent. Surprisingly, it was found that this step did not play a significant role for the shape and stoichiometry of the formed nanodiscs. Finally, the effect of the choice of detergent used in the reconstitution process was investigated. It was found that detergent type is a central determining factor for the shape and stoichiometry of the formed nanodiscs. A significantly increasing POPC/MSP1D1 stoichiometry of the formed nanodiscs was observed as the reconstitution detergent type is changed in the order: Tween80, DDM, Triton X-100, OG, CHAPS, Tween20, and Cholate, but with no simple correlation to the characteristics of the detergent. This emphasizes that the detergents optimal for solution storage and crystallization of membrane proteins, in particular DDM, should not be used alone for nanodisc reconstitution. However, our data also show that when applying mixtures of the reconstitution detergent cholate and the storage detergents DDM or OG, cholate dominates the reconstitution process and nanodiscs are obtained, which resemble those formed without storage detergents.

Entities:  

Year:  2018        PMID: 30239200     DOI: 10.1021/acs.langmuir.8b01503

Source DB:  PubMed          Journal:  Langmuir        ISSN: 0743-7463            Impact factor:   3.882


  10 in total

1.  Nanodisc self-assembly is thermodynamically reversible and controllable.

Authors:  Tyler Camp; Stephen G Sligar
Journal:  Soft Matter       Date:  2020-06-24       Impact factor: 3.679

2.  The hydrodynamic motion of Nanodiscs.

Authors:  Tyler Camp; Mark McLean; Mallory Kato; Lionel Cheruzel; Stephen Sligar
Journal:  Chem Phys Lipids       Date:  2019-02-22       Impact factor: 3.329

3.  Heating-Induced DMPC/Glycyrrhizin Bicelle-to-Vesicle Transition: A X-Ray Contrast Variation Study.

Authors:  Carina Dargel; Yvonne Hannappel; Thomas Hellweg
Journal:  Biophys J       Date:  2020-04-08       Impact factor: 4.033

Review 4.  Nanodiscs: A toolkit for membrane protein science.

Authors:  Stephen G Sligar; Ilia G Denisov
Journal:  Protein Sci       Date:  2020-11-16       Impact factor: 6.993

5.  Structure and dynamics of a nanodisc by integrating NMR, SAXS and SANS experiments with molecular dynamics simulations.

Authors:  Tone Bengtsen; Viktor L Holm; Lisbeth Ravnkilde Kjølbye; Søren R Midtgaard; Nicolai Tidemand Johansen; Giulio Tesei; Sandro Bottaro; Birgit Schiøtt; Lise Arleth; Kresten Lindorff-Larsen
Journal:  Elife       Date:  2020-07-30       Impact factor: 8.140

6.  Global fitting of multiple data frames from SEC-SAXS to investigate the structure of next-generation nanodiscs.

Authors:  Abigail Barclay; Nicolai Tidemand Johansen; Frederik Grønbæk Tidemand; Lise Arleth; Martin Cramer Pedersen
Journal:  Acta Crystallogr D Struct Biol       Date:  2022-03-11       Impact factor: 7.652

7.  Thermodynamically stable vesicle formation of biodegradable double mPEG-tailed amphiphiles with sulfonate head group.

Authors:  Rita Ghosh; Joykrishna Dey; B V N Phani Kumar
Journal:  RSC Adv       Date:  2020-09-02       Impact factor: 3.361

8.  A supramolecular hydrophobic guest transport system based on a biological macrocycle.

Authors:  Yan Ge; Xin Shen; Hongqian Cao; Yuchong Hao; Lin Jin; Jie Shang; Yangxin Wang; Tiezheng Pan; Zhenhui Qi
Journal:  RSC Adv       Date:  2019-11-22       Impact factor: 4.036

9.  Order and disorder-An integrative structure of the full-length human growth hormone receptor.

Authors:  Noah Kassem; Raul Araya-Secchi; Katrine Bugge; Abigail Barclay; Helena Steinocher; Adree Khondker; Yong Wang; Aneta J Lenard; Jochen Bürck; Cagla Sahin; Anne S Ulrich; Michael Landreh; Martin Cramer Pedersen; Maikel C Rheinstädter; Per Amstrup Pedersen; Kresten Lindorff-Larsen; Lise Arleth; Birthe B Kragelund
Journal:  Sci Adv       Date:  2021-06-30       Impact factor: 14.136

10.  Erythro-VLPs: Anchoring SARS-CoV-2 spike proteins in erythrocyte liposomes.

Authors:  Sebastian Himbert; Isabella Passos Gastaldo; Rashik Ahmed; Karla Martinez Pomier; Braeden Cowbrough; Dushyant Jahagirdar; Samantha Ros; Janos Juhasz; Harald D H Stöver; Joaquin Ortega; Giuseppe Melacini; Dawn M E Bowdish; Maikel C Rheinstädter
Journal:  PLoS One       Date:  2022-03-11       Impact factor: 3.240

  10 in total

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