期刊
MOLECULAR BIOLOGY OF THE CELL
卷 19, 期 7, 页码 2936-2948出版社
AMER SOC CELL BIOLOGY
DOI: 10.1091/mbc.E07-10-1019
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资金
- National Institutes of Health ( NIH) [R01 GM-60979]
- NIH-NCRR [1S10RR022588-01, R01 DK0532570]
- Ford Foundation Diversity
The spatial and temporal regulation of the interactions among the similar to 60 proteins required for endocytosis is under active investigation in many laboratories. We have identified the interaction between monomeric clathrin adaptors and endocytic scaffold proteins as a critical prerequisite for the recruitment and/or spatiotemporal dynamics of endocytic proteins at early and late stages of internalization. Quadruple deletion yeast cells (Delta Delta Delta Delta) lacking four putative adaptors, Ent1/2 and Yap1801/2 ( homologues of epsin and AP180/CALM proteins), with a plasmid encoding Ent1 or Yap1802 mutants, have defects in endocytosis and growth at 37 degrees C. Live-cell imaging revealed that the dynamics of the early- and late-acting scaffold proteins Ede1 and Pan1, respectively, depend upon adaptor interactions mediated by adaptor asparagine-proline-phenylalanine motifs binding to scaffold Eps15 homology domains. These results suggest that adaptor/scaffold interactions regulate transitions from early to late events and that clathrin adaptor/scaffold protein interaction is essential for clathrin-mediated endocytosis.
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