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 發報日期 : 2023/12/11 發行期數:324 
 
 
 

最新消息

 
 
 
 
新書展示
 
展期:2023-12-11 ~ 2023-12-18
 
 
 
 
 
 
 
中研院重要研究成果展:湯森林博士
 
題目:揭開珊瑚菌聚體的生態特徵、多源基因體和其潛在功能
展期:12/11/2023-12/24/2023
 
 
 
 
 
 

影音服務

 
 
 
 
新增課程之影音及講義,歡迎線上瀏覽
 
H1 Connect 資料庫介紹(原名Faculty Opinions)
 
 
 
 
 
 

Blog

 
 
 
 
QIAGEN IPA 2023秋季更新
 
二十年來,Reactome組織(reactome.org)一直在建立一個開源、開放查詢、人工校對並經過同儕審視的路徑資料庫,涵蓋了許多物種和主題領域。該組織已經導入與QIAGEN IPA相容的格式,並釋出他們的人類路徑資料庫。在此版本中,IPA已經完全整合了這502條路徑,提供更完整的資料查詢與分析服務。
 
 
 
 
 
 
 

專題報導

 
 
 
 
IUPAC 2023年化學領域10大新興技術-低醣廣效疫苗
 
「藉由設計不同流感病毒HA共同的胺基酸序列(consensus sequence),加上將蛋白表面的醣分子修剪,讓不易突變的部位完全暴露出來,讓免疫系統容易辨識,並保留重要的核心結構,是成功發展可對付多種流感病毒分子疫苗的關鍵。」
 
 
 
 
 
 
 

生命組演講公告

 
 
 
 
12/13 分生所演講
 
講題:Runaway Transcription and Its Genome-Wide Impact
主講者:Dr. Gene-Wei Li (Associate Professor Department of Biology Massachusetts Institute of Technology Cambridge, MA)
時間:2023-12-13 11:00 - 12:00
地點:中央研究院分子生物研究所B1演講廳
 
 
 
 
 
 
 
12/14 生化所演講
 
講題:From Method Development to Total Synthesis of Natural Metabolites for Structure-Activity Relationship Study
主講者:蒙國光教授 (國立陽明交通大學)
時間:2023-12-14 11:00 - 12:00
地點:生化所209室
 
 
 
 
 
 
 
12/14 細生所演講
 
講題:Conserved Cell Fating Mechanisms in Brain Development
主講者:Tzumin Lee, MD, PhD (Peter D. Meister Professor, Life Sciences Institute, Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Howard Hughes Medical Institute)
時間:2023-12-14 11:00 - 12:30
地點:細生所1樓演講廳
 
 
 
 
 
 
 
12/15 生化所演講
 
講題:Deciphering Microbial Influence on Host Behavior and Physiology in Drosophila
主講者:Adam C.N. Wong教授 (美國佛羅里達大學)
時間:2023-12-15 11:00 - 12:00
地點:生化所209室
 
 
 
 
 
 
 
12/18 生化所演講
 
講題:Protein-based fluorescent biosensors for investigating neural metabolism
主講者:Yusuke Nasu教授 (日本東京大學)
時間:2023-12-18 11:00 - 12:00
地點:生化所209室
 
 
 
 
 
 
 
12/18 農生中心演講
 
講題:US Venture Capital 101: Learn about how US VCs pick their winner and how to craft a storyline
主講者:Dr. Hsin-Fang Momo Wu (Chef Business Development Officer, Botrista Technology Inc, USA)
時間:2023-12-18 11:00 - 13:00
地點:本院農業科技大樓1樓A134演講廳
 
 
 
 
 
 
 
12/21 生醫所演講
 
講題:Why microglia belong to the neurovascular unit, and radial glia are NOT the cortical neural progenitors
主講者:Kuan, Chia-Yi (Alex)教授 (Dept. of Neuroscience Univ. of Virginia School of Med., USA)
時間:2023-12-21 11:00 - 12:00
地點:跨領域大樓一樓演講廳
 
 
 
 
 
 
 
12/21 生化所演講
 
講題:Programming bacteria for multiplexed DNA detection
主講者:Yu-Yu Cheng博士 (美國威斯康辛大學麥迪遜分校)
時間:2023-12-21 11:00 - 12:00
地點:生化所209室
 
 
 
 
 
 
 
12/21 生醫所演講
 
講題:Electric Cell-Substrate Impedance Sensing: A Morphological Biosensor for Cell Research
主講者:羅俊民博士 (陽明交通大學)
時間:2023-12-21 16:00 - 17:00
地點:生醫所地下室B1B演講廳
 
 
 
 
 
 

生命組研究成果重要發現

 
 
 
 
高維生素B1的稻米
 
謝明勳老師實驗室最近研發出了高維生素B1的稻米。該研究團隊把一個來自大腸桿菌,與維生素B1合成有關的基因轉殖到水稻與阿拉伯芥中,結果發現轉殖植物內的維生素B1含量提高了。謝老師的研究團隊進一步以具有胚乳專一性的啟動子來驅動該大腸桿菌的基因,結果發現轉殖水稻的糙米與白米增加了約25-30% 的維生素B1。
 
 
 
 
 
 
 
 
治療遺傳性軟骨發育不全矮小症狀新契機
 
曾經想過希望自己可以多長個幾公分嗎?那侏儒症患者呢?本院細胞與個體生物學研究所李宜靜研究團隊,建立一細胞篩選系統,從植物萃取物中分離出有效成分,希望可以幫助侏儒症患者長高。 骨骼生長受到精確調控,纖維細胞生長因子受體 3 (FGFR3) 扮演重要角色。FGFR3 在胎兒發育晚期,骨骼生長板的軟骨細胞中大量表現,抑制胎兒骨骼的生長。
 
 
 
 
 
 
 
 
RAD51 paralogs synergize with RAD51 to protect reversed forks from cellular nucleases
 
Fork reversal is a conserved mechanism to prevent stalled replication forks from collapsing. Formation and protection of reversed forks are two crucial steps in ensuring fork integrity and stability. Five RAD51 paralogs, namely, RAD51B, RAD51C, RAD51D, XRCC2 and XRCC3, which share sequence and structural similarity to the recombinase RAD51, play poorly defined mechanistic roles in these processes.
 
 
 
 
 
 
 
 
Complexation and evolution of cis-prenyltransferase homologues in Cinnamomum kanehirae deduced from kinetic and functional characterizations
 
Eukaryotic dehydrodolichyl diphosphate synthases (DHDDSs), cis-prenyltransferases (cis-PTs) synthesizing precursors of dolichols to mediate glycoprotein biosynthesis require partners, e.g. Nus1 in yeast and NgBR in animals, which are cis-PTs homologues without activity but to boost the DHDDSs activity.
 
 
 
 
 
 
 
 
PHRF1 Promotes Cell Invasion by Modulating SOX4 Expression in Colorectal Cancer HCT116-p53-/- Cells
 
This study sheds light on the role of PHRF1 in the invasion of colorectal cancer HCT116-p53-/- cells, which harbor the oncogenic KrasG13D mutation and lack p53. These findings provide novel insights regarding the role of PHRF1 in invasion by modulating SOX4 expression in colorectal cancer HCT116-p53-/- cells.
 
 
 
 
 
 
 
 
Visualizing the DNA repair process by a photolyase at atomic resolution
 
Photolyases, a ubiquitous class of flavoproteins, use blue light to repair DNA photolesions. In this work, we determined the structural mechanism of the photolyase-catalyzed repair of a cyclobutane pyrimidine dimer (CPD) lesion using time-resolved serial femtosecond crystallography (TR-SFX).
 
 
 
 
 
 
 
 
A structure of the relict phycobilisome from a thylakoid-free cyanobacterium
 
Phycobilisomes (PBS) are antenna megacomplexes that transfer energy to photosystems II and I in thylakoids. PBS likely evolved from a basic, inefficient form into the predominant hemidiscoidal shape with radiating peripheral rods.
 
 
 
 
 
 
 
 
揭開罪魁禍首:小膠質細胞半乳糖凝集素 3 加劇 Tau 蛋白疾病
 
阿茲海默症的關鍵因素包括β澱粉樣蛋白斑塊、過度磷酸化tau (pTau) 和小膠質細胞活化。Galectin-3是一種 β-半乳糖苷結合蛋白,它在tau病理(tauopathy)中的作用仍不清楚。我們的研究顯示Galectin-3在tauopathy的病人和小鼠的小膠質細胞中表達上調。
 
 
 
 
 
 
 
 
發現強勢型釋放氣候冷化氣體的新珊瑚內生桿菌
 
DMSP(dimethylsulfoniopropionate) 是重要全球硫循環分子,主要由海洋植物性浮游生物和微生物產生。珊瑚礁是高DMSP生產棲地,其中不僅浮游生物和微生物製造該分子,珊瑚本身也參與製造DMSP,DMSP代謝被視為珊瑚對抗熱逆境一個重要的機制和手段,其中DMSP分解後的DMS (dimethylsulfide) 是知名的氣候冷化氣體,具有極優的抗氧化能力,可以幫忙珊瑚清除熱逆境引起的大量自由基。
 
 
 
 
 
 
 
 
Structure, dynamics and stability of the smallest and most complex 71 protein knot
 
Proteins can spontaneously tie a variety of intricate topological knots through twisting and threading of the polypeptide chains. Recently developed artificial intelligence algorithms have predicted several new classes of topological knotted proteins, but the predictions remain to be authenticated experimentally.
 
 
 
 
 
 
 
 
An integrative approach unveils a distal encounter site for rPTPε and phospho-Src complex formation
 
The structure determination of protein tyrosine phosphatase (PTP): phospho-protein complexes, which is essential to understand how specificity is achieved at the amino acid level, remains a significant challenge for protein crystallography and cryoEM due to the transient nature of binding interactions.
 
 
 
 
 
 
 
 
 
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