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001026361 1001_ $$0P:(DE-Juel1)181095$$aÜffing, Alina$$b0$$eFirst author
001026361 245__ $$aHighlighting the hidden: monitoring the avidity-driven association of a fluorescent GABARAP tandem with microtubules in living cells
001026361 260__ $$aLondon$$bTaylor & Francis Group$$c2024
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001026361 500__ $$aThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
001026361 520__ $$aGABARAP, like other ATG8 proteins, is a ubiquitin-like modifier and its C-terminal lipid conjugation enables association with cellular membranes. To prevent interference with the lipidation process, N-terminal fluorescent protein (FP) tagging strategies have become the standard for studying ATG8 localization and function in living cells, significantly contributing to our understanding of this protein family’s multifaceted roles. We employed live cell imaging with particular emphasis on a GABARAP split-tandem construct, GABARAP(G116A)-mTagBFP2-GABARAP (G-B-G), which retains both a free N-terminus and a lipidation-competent c-terminus, while bivalence creates a gain in affinity conferred by avidity. Notably, reminiscent of early in vitro studies demonstrating an interaction of GABARAP and tubulin, our results revealed a robust association of G-B-G with the microtubule network in living cells. We show that the presence of several basic residues in the amino-terminal helical subdomain of GABARAP and avidity emerged as essential for robust MT association, whereas lipidation ability was not decisive. Interestingly, while the position of the FP-tag had little influence on the result, the nature of the FP itself was crucial, with mTagBFP2 being required for tracking GABARAP tandems in the vicinity of MTs. Though artificial effects cannot be excluded, we assume that G-B-G, with its increased avidity, can give visibility to processes that are based on inherently weak interactions, and thus can help elucidate potential roles of GABARAP e.g. in microtubule-associated processes that are integral to autophagy-related and -unrelated cellular transport.
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001026361 7001_ $$aGold, Lisa$$b1
001026361 7001_ $$0P:(DE-Juel1)131924$$aGensch, Thomas$$b2
001026361 7001_ $$0P:(DE-Juel1)131988$$aWeiergräber, Oliver H.$$b3
001026361 7001_ $$0P:(DE-Juel1)132003$$aHoffmann, Silke$$b4$$eCorresponding author
001026361 7001_ $$0P:(DE-Juel1)132029$$aWillbold, Dieter$$b5
001026361 773__ $$0PERI:(DE-600)3122278-X$$a10.1080/27694127.2024.2348899$$gVol. 3, no. 1, p. 2348899$$n1$$p2348899$$tAutophagy reports$$v3$$x2769-4127$$y2024
001026361 8564_ $$uhttps://doi.org/10.1080/27694127.2024.2348899
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