Susan Hamamoto
Overview
Explore the profile of Susan Hamamoto including associated specialties, affiliations and a list of published articles.
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12
Citations
1310
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Recent Articles
1.
Jin Y, Sultana A, Gandhi P, Franklin E, Hamamoto S, Khan A, et al.
Dev Cell
. 2011 Dec;
21(6):1156-70.
PMID: 22172676
Vesicle transport requires four steps: vesicle formation, movement, tethering, and fusion. In yeast, two Rab GTPases, Ypt31/32, are required for post-Golgi vesicle formation. A third Rab GTPase, Sec4, and the...
2.
Kung L, Pagant S, Futai E, DArcangelo J, Buchanan R, Dittmar J, et al.
EMBO J
. 2011 Dec;
31(4):1014-27.
PMID: 22157747
Vesicle budding from the endoplasmic reticulum (ER) employs a cycle of GTP binding and hydrolysis to regulate assembly of the COPII coat. We have identified a novel mutation (sec24-m11) in...
3.
Fromme J, Ravazzola M, Hamamoto S, Al-Balwi M, Eyaid W, Boyadjiev S, et al.
Dev Cell
. 2007 Nov;
13(5):623-634.
PMID: 17981132
Proteins trafficking through the secretory pathway must first exit the endoplasmic reticulum (ER) through membrane vesicles created and regulated by the COPII coat protein complex. Cranio-lenticulo-sutural dysplasia (CLSD) was recently...
4.
Wang C, Hamamoto S, Orci L, Schekman R
J Cell Biol
. 2006 Sep;
174(7):973-83.
PMID: 17000877
A yeast plasma membrane protein, Chs3p, transits to the mother-bud neck from a reservoir comprising the trans-Golgi network (TGN) and endosomal system. Two TGN/endosomal peripheral proteins, Chs5p and Chs6p, and...
5.
Boyadjiev S, Fromme J, Ben J, Chong S, Nauta C, Hur D, et al.
Nat Genet
. 2006 Sep;
38(10):1192-7.
PMID: 16980979
Cranio-lenticulo-sutural dysplasia (CLSD) is an autosomal recessive syndrome characterized by late-closing fontanels, sutural cataracts, facial dysmorphisms and skeletal defects mapped to chromosome 14q13-q21 (ref. 1). Here we show, using a...
6.
Lee M, Orci L, Hamamoto S, Futai E, Ravazzola M, Schekman R
Cell
. 2005 Aug;
122(4):605-17.
PMID: 16122427
Secretory proteins traffic from the ER to the Golgi via COPII-coated transport vesicles. The five core COPII proteins (Sar1p, Sec23/24p, and Sec13/31p) act in concert to capture cargo proteins and...
7.
Kim J, Hamamoto S, Ravazzola M, Orci L, Schekman R
J Biol Chem
. 2004 Dec;
280(9):7758-68.
PMID: 15623526
Mutant forms of presenilin (PS) 1 and 2 and amyloid precursor protein (APP) lead to familial Alzheimer's disease. Several reports indicate that PS may modulate APP export from the endoplasmic...
8.
Futai E, Hamamoto S, Orci L, Schekman R
EMBO J
. 2004 Oct;
23(21):4146-55.
PMID: 15457212
The generation of COPII vesicles from synthetic liposome membranes requires the minimum coat components Sar1p, Sec23/24p, Sec13/31p, and a nonhydrolyzable GTP analog such as GMP-PNP. However, in the presence of...
9.
Miller E, Beilharz T, Malkus P, Lee M, Hamamoto S, Orci L, et al.
Cell
. 2003 Aug;
114(4):497-509.
PMID: 12941277
We have characterized the mechanisms of cargo selection into ER-derived vesicles by the COPII subunit Sec24p. We identified a site on Sec24p that recognizes the v-SNARE Bet1p and show that...
10.
Miller E, Antonny B, Hamamoto S, Schekman R
EMBO J
. 2002 Nov;
21(22):6105-13.
PMID: 12426382
Transport of secretory proteins out of the endoplasmic reticulum (ER) is mediated by vesicles generated by the COPII coat complex. In order to understand how cargo molecules are selected by...