Ride the wave: Retrograde trafficking becomes Ca(2+) dependent with BAIAP3

Research output: Contribution to journal › Comment/debate › Research

Standard

Ride the wave : Retrograde trafficking becomes Ca(2+) dependent with BAIAP3. / Sørensen, Jakob B.

In: Journal of Cell Biology, Vol. 216, No. 7, 2017, p. 1887-1889.

Research output: Contribution to journal › Comment/debate › Research

Harvard

Sørensen, JB 2017, 'Ride the wave: Retrograde trafficking becomes Ca(2+) dependent with BAIAP3', Journal of Cell Biology, vol. 216, no. 7, pp. 1887-1889. https://doi.org/10.1083/jcb.201706007

APA

Sørensen, J. B. (2017). Ride the wave: Retrograde trafficking becomes Ca(2+) dependent with BAIAP3. Journal of Cell Biology, 216(7), 1887-1889. https://doi.org/10.1083/jcb.201706007

Vancouver

Sørensen JB. Ride the wave: Retrograde trafficking becomes Ca(2+) dependent with BAIAP3. Journal of Cell Biology. 2017;216(7):1887-1889. https://doi.org/10.1083/jcb.201706007

Author

Sørensen, Jakob B. / Ride the wave : Retrograde trafficking becomes Ca(2+) dependent with BAIAP3. In: Journal of Cell Biology. 2017 ; Vol. 216, No. 7. pp. 1887-1889.

Bibtex

@article{59fb723f0d5a46c980dce51af34d6bd6,
title = "Ride the wave: Retrograde trafficking becomes Ca(2+) dependent with BAIAP3",
abstract = "The functions of four of the five proteins in the mammalian uncoordinated-13 (Munc13) family have been identified as priming factors in SNARE-dependent exocytosis. In this issue, Zhang et al. (2017. J. Cell Biol. https://doi.org/10.1083/jcb.201702099) show that the fifth member, BAIAP3 (brain-specific angiogenesis inhibitor I-associated protein 3), acts in retrograde trafficking by returning secretory vesicle material to the trans-Golgi network. In its absence, secretory vesicle formation is impaired, leading to accumulation of immature vesicles, or lysosomal vesicle degradation.",
keywords = "Animals, Exocytosis, Protein Transport, SNARE Proteins, Secretory Vesicles, trans-Golgi Network, Journal Article",
author = "S{\o}rensen, {Jakob B}",
note = "{\textcopyright} 2017 S{\o}rensen.",
year = "2017",
doi = "10.1083/jcb.201706007",
language = "English",
volume = "216",
pages = "1887--1889",
journal = "Journal of Cell Biology",
issn = "0021-9525",
publisher = "Rockefeller University Press",
number = "7",

}

RIS

TY - JOUR

T1 - Ride the wave

T2 - Retrograde trafficking becomes Ca(2+) dependent with BAIAP3

AU - Sørensen, Jakob B

N1 - © 2017 Sørensen.

PY - 2017

Y1 - 2017

N2 - The functions of four of the five proteins in the mammalian uncoordinated-13 (Munc13) family have been identified as priming factors in SNARE-dependent exocytosis. In this issue, Zhang et al. (2017. J. Cell Biol. https://doi.org/10.1083/jcb.201702099) show that the fifth member, BAIAP3 (brain-specific angiogenesis inhibitor I-associated protein 3), acts in retrograde trafficking by returning secretory vesicle material to the trans-Golgi network. In its absence, secretory vesicle formation is impaired, leading to accumulation of immature vesicles, or lysosomal vesicle degradation.

AB - The functions of four of the five proteins in the mammalian uncoordinated-13 (Munc13) family have been identified as priming factors in SNARE-dependent exocytosis. In this issue, Zhang et al. (2017. J. Cell Biol. https://doi.org/10.1083/jcb.201702099) show that the fifth member, BAIAP3 (brain-specific angiogenesis inhibitor I-associated protein 3), acts in retrograde trafficking by returning secretory vesicle material to the trans-Golgi network. In its absence, secretory vesicle formation is impaired, leading to accumulation of immature vesicles, or lysosomal vesicle degradation.

KW - Animals

KW - Exocytosis

KW - Protein Transport

KW - SNARE Proteins

KW - Secretory Vesicles

KW - trans-Golgi Network

KW - Journal Article

U2 - 10.1083/jcb.201706007

DO - 10.1083/jcb.201706007

M3 - Comment/debate

C2 - 28626002

VL - 216

SP - 1887

EP - 1889

JO - Journal of Cell Biology

JF - Journal of Cell Biology

SN - 0021-9525

IS - 7

ER -

ID: 185030281