Zhaohan Lin, ¹ Yinglin Li, ¹ Yuqi Hang, ¹ Changhe Wang, ¹ Bing Liu, ¹ Jie Li, ¹ Lili Yin, ¹ Xiaohan Jiang, ¹ Xingyu Du, ¹ Zhongjun Qiao, ¹ Feipeng Zhu, ¹ Zhe Zhang, ¹ Quanfeng Zhang, ¹ and Zhuan Zhou¹

Abstract: Large dense‐core vesicles (LDCVs) are larger in volume than synaptic vesicles, and are filled with multiple neuropeptides, hormones, and neurotransmitters that participate in various physiological processes. However, little is known about the mechanism determining the size of LDCVs. Here, it is reported that secretogranin II (SgII), a vesicle matrix protein, contributes to LDCV size regulation through its liquid–liquid phase separation in neuroendocrine cells. First, SgII undergoes pH‐dependent polymerization and the polymerized SgII forms phase droplets with Ca2+ in vitro and in vivo. Further, the Ca2+‐induced SgII droplets recruit reconstituted bio‐lipids, mimicking the LDCVs biogenesis. In addition, SgII knockdown leads to significant decrease of the quantal neurotransmitter release by affecting LDCV size, which is differently rescued by SgII truncations with different degrees of phase separation. In conclusion, it is shown that SgII is a unique intravesicular matrix protein undergoing liquid–liquid phase separation, and present novel insights into how SgII determines LDCV size and the quantal neurotransmitter release.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9507364/