| Literature DB >> 21194369 |
Rosa L López-Marqués1, Joost C M Holthuis, Thomas G Pomorski.
Abstract
While accumulating evidence indicates that P4-ATPases catalyze phospholipid transport across cellular bilayers, their kinship to cation-pumping ATPases has raised fundamental questions concerning the underlying flippase mechanism. Loss of P4-ATPase function perturbs vesicle formation in late secretory and endocytic compartments. An intriguing concept is that P4-ATPases help drive vesicle budding by generating imbalances in transbilayer lipid numbers. Moreover, activation of P4-ATPases by phosphoinositides and other effectors of coat recruitment provide a potential mechanism to confine flippase activity to sites of vesicle biogenesis. These developments have raised considerable interest in understanding the mechanism, regulation and biological implications of P4-ATPase-catalyzed phospholipid transport.Entities:
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Year: 2011 PMID: 21194369 DOI: 10.1515/BC.2011.015
Source DB: PubMed Journal: Biol Chem ISSN: 1431-6730 Impact factor: 3.915