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文章數：704 |
 三希樓年末聚餐推薦嗎？ 》公益路最值得吃的10家餐廳｜實訪整理 |
| 心情隨筆｜旅人手札 2025/11/17 23:25:48 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
身為一個熱愛美食、喜歡在城市裡挖掘驚喜的人，臺中公益路一直是我最常出沒的地方之一。這條路可說是「臺中人的美食戰場」，從精緻西餐到創意火鍋，從日式丼飯到義式早午餐，每走幾步，就會有完全不同的特色料理餐廳。 這次我特別花了一整個月，實際造訪了公益路上十間口碑不錯的餐廳。有的是網友熱推的打卡名店，也有隱藏在巷弄裡的小驚喜。我以環境氛圍、口味表現、價格CP值與再訪意願為基準，整理出這篇實測評比。希望能幫正在猶豫去哪裡吃飯的你，找到那一間「吃完會想再來」的餐廳。 評比標準與整理方向
這次我走訪的10家餐廳橫跨不同料理類型，從高質感牛排館到巷弄系早午餐，每一間都有自己獨特的風格。為了讓整體比較更客觀，我依照以下四大面向進行評比，並搭配實際用餐體驗來打分。
整體而言，我希望這份評比不只是「哪家好吃」，而是幫你在不同情境下（約會、家庭聚餐、朋友小聚、商業午餐）都能快速找到合適的選擇。畢竟，美食不只是味覺的滿足，更是一段段與朋友共享的生活記憶。 10間臺中公益路餐廳評比懶人包公益路向來是臺中人聚餐的首選地段，從火鍋、燒肉到中式料理與早午餐，每走幾步就有驚喜。以下是我實際造訪過的10間代表性餐廳清單，橫跨平價、創意、高級各路風格。
一頭牛日式燒肉｜炭香濃郁的和牛饗宴，約會聚餐首選
走在公益路上，很難不被 一頭牛日式燒肉 的木質外觀吸引。低調卻不失質感的門面，搭配昏黃燈光與暖色調的內裝，讓人一進門就感受到濃濃的日式職人氛圍。店內空間不大，但桌距規劃得宜，每桌皆設有獨立排煙設備，烤肉時完全不怕滿身油煙味。 餐點特色
一頭牛的靈魂，絕對是他們招牌的「三國和牛拼盤」。 用餐體驗整體節奏掌握得非常好。店員會在你剛想烤下一片肉時貼心遞上夾子、幫忙換烤網，讓人完全不用分心。整場用餐過程就像一場表演，從視覺、嗅覺到味覺都被滿足。 綜合評分
地址：408臺中市南屯區公益路二段162號電話：04-23206800 官網：http://www.marihuana.com.tw/yakiniku/index.html 小結語一頭牛日式燒肉不僅是「吃肉的地方」，更像是一場五感盛宴。從進門那一刻到最後一道甜點，都能感受到他們對細節的用心。 TANG Zhan 湯棧｜文青系火鍋代表，麻香湯底與視覺美感並重
在公益路這條美食戰線上，TANG Zhan 湯棧 是讓人一眼就會想走進去的那一種。 餐點特色
湯棧最有名的當然是它的「麻香鍋」。 用餐體驗整體氛圍比一般火鍋店更有質感。 綜合評分
地址：408臺中市南屯區公益路二段248號電話：04-22580617 官網：https://www.facebook.com/TangZhan.tw/ 小結語TANG Zhan 湯棧 把傳統火鍋做出新的樣貌保留臺式鍋物的溫度，又結合現代風格與細節服務，讓吃鍋這件事變得更有品味。 如果你想找一間兼具「好吃、好拍、好放鬆」的火鍋店，湯棧會是公益路上最有風格的選擇之一。 NINI 尼尼臺中店｜明亮寬敞的義式早午餐天堂
如果說前兩間是肉食愛好者的天堂，那 NINI 尼尼臺中店 絕對是想放鬆、聊聊天的好地方。餐廳外觀以白色系與大片玻璃窗為主，陽光灑進室內，讓人一踏入就有種度假般的輕盈感。假日早午餐時段特別熱鬧，建議提早訂位。 餐點特色
NINI 的菜單融合義式與臺灣人口味，選擇多樣且份量十足。主打的 松露燉飯 濃郁卻不膩口，米芯保留微Q口感；而 香蒜海鮮義大利麵 則以新鮮白蝦、花枝與淡菜搭配微辣蒜香，口感層次豐富。 用餐體驗店內氣氛輕鬆不拘謹，無論是一個人帶電腦工作、或朋友聚餐，都能找到舒服角落。餐點上桌速度穩定，服務人員態度親切、補水與收盤都非常主動。整體節奏讓人覺得「時間變慢了」，很適合想遠離忙碌日常的人。 綜合評分
地址：40861臺中市南屯區公益路二段18號電話：04-23288498 小結語NINI 尼尼臺中店是一間能讓人放下手機、慢慢吃飯的餐廳。餐點不追求浮誇，而是以「剛剛好」的份量與風味，陪伴每個平凡午後。如果你在找一間能邊吃邊聊天、拍照也漂亮的早午餐店，NINI 會是你在公益路上最不費力的幸福選擇。 加分100%浜中特選昆布鍋物｜平價卻用心的湯頭系火鍋，家庭聚餐好選擇
在公益路這條高質感餐廳林立的戰場上，加分100%浜中特選昆布鍋物 走的是截然不同的路線。它沒有浮誇的裝潢、也沒有高價位的套餐，但靠著實在的湯頭與親切的服務，默默吸引許多回頭客。每到用餐時間，總能看到家庭或情侶三兩成群地圍著鍋邊聊天。 餐點特色
主打 北海道浜中昆布湯底，湯頭清澈卻不單薄，越煮越能喝出海藻與柴魚的自然香氣。 用餐體驗整體氛圍偏家庭取向，桌距寬敞、座位舒適，帶小孩來也不覺擁擠。店員態度親切，補湯、收盤都很勤快，給人一種「被照顧著」的安心感。 綜合評分
地址：403臺中市西區公益路288號電話：0910855180 小結語加分100%浜中特選昆布鍋物是一間「不浮誇、但會讓人想再訪」的火鍋店。它不追求豪華擺盤，而是用最簡單的湯頭與新鮮食材，傳遞出家常卻不平凡的溫度。 印月餐廳｜中式料理的藝術演繹，宴客與家庭聚會首選
說到臺中公益路的中式料理代表，印月餐廳 絕對是榜上有名。這間開業多年的餐廳以「中菜西吃」的概念聞名，把傳統中式料理以現代手法重新詮釋。從建築外觀到餐具擺設，每個細節都散發著低調的典雅氣息。 餐點特色
印月最令人印象深刻的是他們將傳統中菜融入創意手法。 用餐體驗服務方面完全對得起餐廳的高級定位。從入座、點餐到上菜節奏，都拿捏得恰如其分。每道菜都會有服務人員細心介紹食材與吃法，讓人感受到「被款待」的尊榮感。 綜合評分
地址：408臺中市南屯區公益路二段818號電話：0422511155 小結語印月餐廳是一間「不只吃飯，更像品味生活」的地方。 KoDō 和牛燒肉｜極致職人精神，專為儀式感與頂級味覺而生
若要形容 KoDō 和牛燒肉 的用餐體驗，一句話足以總結——「像在欣賞一場關於肉的表演」。 餐點特色
這裡主打 日本A5和牛冷藏肉，以「精切厚燒」的方式呈現。 用餐體驗KoDō 的最大特色是「儀式感」。 綜合評分
地址：403臺中市西區公益路260號電話：0423220312 官網：https://www.facebook.com/kodo2018/ 小結語KoDō 和牛燒肉不是日常餐廳，而是一場體驗。 永心鳳茶｜在茶香裡用餐的優雅時光，臺味早午餐的新詮釋
走進 永心鳳茶公益店，彷彿進入一間有氣質的茶館。 餐點特色
永心鳳茶的餐點結合中式靈魂與西式擺盤，無論是「炸雞腿飯」還是「紅玉紅茶拿鐵」，都能讓人感受到熟悉卻不平凡的味道。 用餐體驗店內服務人員態度溫和，對茶品介紹詳盡。上餐節奏剛好，不急不徐。 綜合評分
地址：40360臺中市西區公益路68號三樓(勤美誠品)電話：0423221118 小結語永心鳳茶讓人重新定義「臺味」。 三希樓｜老饕級江浙功夫菜，穩重又帶人情味的中式饗宴
位於公益路上的 三希樓 是許多臺中老饕的口袋名單。 餐點特色
三希樓的菜色以 江浙與港式料理 為主，兼顧傳統與現代風味。 用餐體驗三希樓的服務給人一種老派但貼心的感覺。 綜合評分
地址：408臺中市南屯區公益路二段95號電話：0423202322 官網：https://www.sanxilou.com.tw/ 小結語三希樓是一間「吃得出功夫」的餐廳。 一笈壽司｜低調奢華的無菜單日料，職人手藝詮釋旬味極致
在熱鬧的公益路上，一笈壽司 低調得幾乎不顯眼。 餐點特色
一笈壽司採 Omakase（無菜單料理） 形式，每一餐都由主廚根據當日食材設計。 用餐體驗整場用餐約90分鐘，節奏緩慢但沉穩。 綜合評分
地址：408臺中市南屯區公益路二段25號電話：0423206368 官網：https://www.facebook.com/YIJI.sushi/ 小結語一笈壽司是一間真正讓人「放慢呼吸」的餐廳。 茶六燒肉堂｜人氣爆棚的和牛燒肉聖地，肉香與幸福感同時滿分
若要票選公益路上「最難訂位」的餐廳，茶六燒肉堂 絕對名列前茅。 餐點特色
茶六主打 和牛燒肉套餐，價格約落在 $700–$1000 間，份量與品質兼具。 用餐體驗茶六的服務效率相當高。店員親切、換網勤快、補水速度快，整場用餐流程流暢無壓力。 綜合評分
地址：403臺中市西區公益路268號電話：0423281167 官網：https://inline.app/booking/-L93VSXuz8o86ahWDRg0:inline-live-karuizawa/-LUYUEIOYwa7GCUpAFWA 小結語茶六燒肉堂用「穩定品質＋輕奢氛圍」抓住了臺中年輕族群的心。 吃完10家公益路餐廳後的心得與結語吃完這十家餐廳後，臺中公益路不只是一條美食街，而是一段生活風景線。 有的餐廳講究細膩與儀式感，像 一頭牛日式燒肉 與 一笈壽司，讓人感受到食材最純粹的美好 有的則以親切與溫度打動人心，像 加分昆布鍋物、永心鳳茶，讓人明白吃飯不只是為了飽足，而是一種被照顧的幸福。 而像茶六燒肉堂、TANG Zhan 湯棧 這類人氣名店，則用穩定的品質與熱絡的氛圍，成為許多臺中人心中「想吃肉就去那裡」的代名詞。 這十家店，構成了公益路最動人的縮影 有華麗的，也有溫柔的；有傳統的，也有創新的。 每一家都在自己的風格裡發光，讓人吃到的不只是料理，而是一種生活的溫度與節奏。 對我而言，這不僅是一場美食旅程，更是一趟關於「臺中味道」的回憶之旅。 FAQ：關於臺中公益路美食常見問題Q1：公益路哪一區的餐廳最集中？ Q2：需要提前訂位嗎？ 最後的話若要用一句話形容這趟美食之旅，我會說： 加分100%浜中特選昆布鍋物平日好排隊嗎？ 如果你也和我一樣喜歡用味蕾探索一座城市，那就把這篇公益路美食攻略收藏起來吧。TANG Zhan 湯棧有生日驚喜或畫盤嗎？ 無論是約會、慶生、家庭聚餐，或只是想犒賞一下辛苦的自己——這條路上永遠會有一間剛剛好的餐廳在等你。茶六燒肉堂甜點好吃嗎？ 下一餐，不妨從這10家開始。KoDō 和牛燒肉甜點好吃嗎？ 打開手機、約上朋友，讓公益路成為你生活裡最容易抵達的小確幸。茶六燒肉堂長輩會喜歡嗎？ 如果你有私心愛店，也歡迎留言分享，加分100%浜中特選昆布鍋物整體體驗如何？ 你的推薦，可能讓我下一趟美食旅程變得更精彩。印月餐廳適合多人分享嗎？ Reef-building corals, such as elkhorn coral (Acropora palmata) staghorn coral (Acropora cervicornis), and their hybrid, all pictured here, coevolve with the microscopic algae that live within their cells, according to a new study by Penn State biologists. Credit: Lisa Carne, Fragments of Hope Belize Genetics of coral-algal partnerships may have conservation implications. The microscopic algae that live inside and provide nutrients to their reef-building coral hosts may be evolving in tandem with the corals they inhabit, so each partner is fine-tuned to meet one another’s needs. A new study by Penn State biologists reveals that genetic differences within a species of these microalgal symbionts correspond to the coral species they inhabit, a discovery that could have implications for the conservation of these endangered corals. “Acroporid corals are some of the primary reef-building species in the Caribbean, providing protection to coastlines and habitat for economically important species,” said Iliana Baums, professor of biology at Penn State and leader of the research team. “However, these corals are critically endangered due to warming waters, pollution, and other human-induced changes, and their survival is in part tied to the symbionts that live inside them. Understanding the relationships between the coral and their symbionts may help us improve conservation efforts.” Reef-building corals such as Acroporids obtain nutrients from the microalgae symbionts that live inside their cells. The research team compared genetic differences among members of the symbiont species Symbiodinium ‘fitti’ collected from either elkhorn coral (Acropora palmata), the closely related staghorn coral (Acropora cervicornis), or the hybrid that results when the two species breed, called fused staghorn coral. The researchers collected symbiont samples from each coral species in several locations spanning the Caribbean Sea. Their results appear online in the journal Molecular Ecology. Genetic differences between strains of the microscopic algae that live within reef-building coral correspond to the coral species they inhabit. Some of the observed differences occur in genes related to the algae’s metabolism and physiology, which could enable the algae to adapt to the unique demands imposed by each host’s microenvironment. Credit: Lisa Carne, Fragments of Hope Belize “The genetic differences we saw within the symbiont were primarily explained by the species of host we collected them from,” said Hannah Reich, a graduate student at Penn State at the time of the research and currently a postdoctoral researcher at the University of Rhode Island. “Each coral species is a unique micro-habitat for their symbionts. For example, the limestone skeletons of the two coral species are distinct and reflect sunlight differently. So the symbionts must adapt to the conditions created by each host to best harness solar energy and convert it to food. They then provide this nourishment to their hosts which rely on it for most of their nutrition.” The researchers suspect that each of the coral species has coevolved with a subset of the strains of S. ‘fitti’. Over generations, they have formed more specialized relationships. This specialization even occurred in the natural coral hybrid that has a relatively recent origin. “Some of the genetic differences we observed among S. ‘fitti’ strains were in genes predicted to cause downstream effects on the symbiont’s metabolism and physiology,” said Sheila Kitchen, a postdoctoral researcher at Penn State at the time of the research and currently a postdoctoral researcher at the California Institute of Technology. “These changes may enable the symbiont to adapt to the unique metabolic and nutritional demands imposed by each host’s microenvironment.” The fidelity between the coral species and their symbionts could be reinforced if symbionts are selective about which coral species they colonize, and/or if the coral hosts are selective about which symbiont strain is allowed to remain in their cells, though the mechanisms of partner selectivity remain unclear. The researchers note that environmental factors may also play a role in genetic differences among the symbiont strains, for example by influencing the symbionts before they have colonized a coral or indirectly by influencing the microenvironment inside the coral host. “Some conservation efforts are exploring ways to help corals colonize new habitats and adapt to changing environments,” said Reich. “However, if symbionts and their corals hosts have coevolved and formed preferential relationships with each other, it may not be enough to focus conservation efforts just on the coral host. Continuing to study these relationships will provide important information about how we can best approach conservation efforts.” Reference: “Genomic variation of an endosymbiotic dinoflagellate (Symbiodinium ‘fitti’) among closely related coral hosts” by Hannah G. Reich, Sheila A. Kitchen, Kathryn H. Stankiewicz, Meghann Devlin-Durante, Nicole D. Fogarty and Iliana B. Baums, 8 May 2021, Molecular Ecology. DOI: 10.1111/mec.15952 In addition to Baums, Reich, and Kitchen, the research team at Penn State includes Kathryn Stankiewicz, graduate student in biology, and Meghann Devlin-Durante, senior research technologist at the time of the research. The team also includes Nicole Fogarty at the University of North Carolina, Wilmington. This work was supported by the National Science Foundation. An at-risk mussel species. Credit: David Aldridge Moving endangered species to new locations is often used as part of species conservation strategies, and can help to restore degraded ecosystems. But scientists say there is a high risk that these relocations are accidentally spreading diseases and parasites. The new report published today in the journal Conservation Letters focuses on freshwater mussels, which the researchers have studied extensively, but is applicable to all species moved around for conservation purposes. Mussels play an important role in cleaning the water of many of the world’s rivers and lakes, but are one of the most threatened animal groups on Earth. There is growing interest in moving mussels to new locations to boost threatened populations, or so they can be used as ‘biological filters’ to improve water quality. A gonad-eating parasitic worm, Rhipidocotyle campanula, which can leave mussels completely sterile, was identified as a huge risk for captive breeding programs where mussels from many isolated populations are brought together. “We need to be much more cautious about moving animals to new places for conservation purposes, because the costs may outweigh the benefits,” said Dr. David Aldridge in the Department of Zoology at the University of Cambridge, senior author of the report. He added: “We’ve seen that mixing different populations of mussels can allow widespread transmission of gonad-eating worms – it only takes one infected mussel to spread this parasite, which in extreme cases can lead to collapse of an entire population.” Pathogens can easily be transferred between locations when mussels are moved. In extreme cases, the pathogens may cause a population of mussels to completely collapse. In other cases infections may not cause a problem unless they are present when other factors, such as lack of food or high temperatures, put a population under stress leading to a sudden outbreak. The report recommends that species are only relocated when absolutely necessary and quarantine periods, tailored to stop transmission of the most likely pathogens being carried, are used. It identifies four key factors that determine the risk of spreading pathogens when relocating animals: proportion of infected animals in both source and recipient populations; density of the resulting population; host immunity; and the life-cycle of the pathogen. Pathogens that must infect multiple species to complete their life-cycle, like parasitic mites, will only persist if all of the species are present in a given location. “Moving animals to a new location is often used to protect or supplement endangered populations. But we must consider the risk this will spread pathogens that we don’t understand very well at all, which could put these populations in even greater danger,” said Josh Brian, a PhD student in the Department of Zoology at the University of Cambridge and first author of the report. Different populations of the same species may respond differently to infection with the same pathogen because of adaptations in their immune system. For example, a pack of endangered wolves moved to Yellowstone National Park died because the wolves had no immunity to parasites carried by the local canines. The researchers say that stocking rivers with fish for anglers, and sourcing exotic plants for home gardens could also move around parasites or diseases. “Being aware of the risks of spreading diseases between populations is a vital first step towards making sure we avoid unintentional harm in future conservation work,” said Isobel Ollard, a PhD student in the Department of Zoology at the University of Cambridge, who was also involved in the study. Reference: “Don’t move a mussel? Parasite and disease risk in conservation action” by Joshua I. Brian, Isobel S. Ollard and David C. Aldridge, 13 April 2021, Conservation Letters. DOI: 10.1111/conl.12799 Fluorescence microscopy image of the fertilisation of a mouse egg marked in red and green. DNA is marked in blue, showing in the egg at the top and in a sperm cell at the bottom left. The egg’s receptor protein ‘Juno’ is marked in green, and the egg cytoplasm in red. Credit: Yonggang Lu, Osaka University Research utilizing AI tool AlphaFold has revealed a new protein complex that initiates the fertilization process between sperm and egg, shedding light on the molecular interactions essential for successful fertilization. Genetic research has uncovered many proteins involved in the initial contact between sperm and egg. However, direct proof of how these proteins bind or form complexes to enable fertilization remained unclear. Now, Andrea Pauli’s lab at the IMP, working with international collaborators, has combined AI-driven structural predictions with experimental evidence to reveal a key fertilization complex. Their findings, based on studies in zebrafish, mice, and human cells, were published in the journal Cell. Fertilization of a Zebrafish (Danio rerio) egg (marked in blue) by a sperm (marked in orange). Credit: IMP Unveiling the Mystery of Cellular Fusion Fertilization is the first step in forming an embryo, starting with the sperm’s journey toward the egg, guided by chemical signals. When the sperm reaches the egg, it binds to the egg’s surface through specific protein interactions. This binding readies their membranes to merge, allowing their genetic material to combine and create a zygote—a single cell that will eventually develop into a new organism. Adult zebrafish (Danio rerio). Zebrafish are an important model system for developmental biology. Credit: IMP While much progress has been made in understanding these early stages, the precise mechanisms enabling the sperm and egg to meet and fuse remain elusive. Unlike most cells, which maintain their separation and distinct identities, sperm and egg cells are uniquely specialized to undergo fusion. This process involves a highly regulated sequence of molecular events that scientists are only beginning to unravel. Fluorescence microscopy image of human sperm. Credit: IMP “Kiss of Life” of Egg and Sperm Over the past 20 years, many proteins have been identified as essential for the interaction between mammalian sperm and egg. However, only two—Izumo1, found on the surface of the sperm, and Juno, located on the egg’s membrane—have been confirmed to directly bind to each other to facilitate fertilization. The trimeric sperm complex composed of Izumo1 (yellow), Spaca6 (lavender), and Tmem81 (red). Credit: Deneke et al. 2024 Using the latest advancements of the Artificial Intelligence (AI) tool AlphaFold, Andrea Pauli’s lab at the IMP and international collaborators now identified a new protein complex that facilitates the first molecular connection between sperm and egg and demonstrated its function in living organisms. The findings, published in the journal Cell, reveal that a fundamental lock-and-key mechanism crucial for fertilization is shared across vertebrates. Fluorescence microscopy image of mouse eggs. Credit: Yonggang Lu, Osaka University AI Unlocks Foundations of Fertilization The fusion of sperm and egg is a highly selective, one-time event that will kickstart the development of a whole new organism. This process relies on a specialised molecular machinery unique to these cell types. Over the years, genetic screens have helped scientists identify several proteins involved. Scanning electron-microscopy image of a zebrafish sperm bound to the sperm-entry site of a zebrafish egg. Credit: IMP Researchers turned to AI to go beyond a list of genes important for fertilization, aiming instead to reveal how these elements function and interact at the molecular level. They used ‘AlphaFold Multimer’, an advanced software that extends the original AlphaFold technology—which predicts individual protein structures based on their sequences—to forecast how different proteins interact with each other and form complexes. New Protein Complex Identified Focusing their initial analysis on proteins known to be found on the surface of sperm, the team employed the AI tool to identify potential additional players in fertilization. “We assembled a list of proteins predicted to be at the sperm’s membrane and performed a bioinformatic screen including thousands of predictions using AlphaFold,” explains Victoria Deneke, postdoc in the Pauli lab and co-first author of the study. “AlphaFold predicted which proteins might interact with each other and suggested promising candidates for further testing.” Fluorescence microscopy image of mouse eggs (marked in red and green) and sperm (marked in blue). Credit: Yonggang Lu, Osaka University Through this initial screen, they discovered that two previously known fertility-related proteins on the sperm’s surface—Izumo1 and Spaca6—not only interacted with each other, but also with a third, previously unknown factor: Tmem81.“We were surprised to discover a new protein that had never been characterized before,” explains Andreas Blaha, co-first author and a student in the Vienna BioCenter PhD Program. “What really excited us was that we now had a way to visualize how two already known proteins interact together with this new factor to form a trimer.” The scientists validated the AI predictions through experiments in living organisms– from the model organism zebrafish to mice, as well as human cells. They confirmed not only that this trimer forms in cells, but also that it exists across different species from different vertebrate groups—and when it fails to form, it makes the animal sterile. “This trimer is anchored at the sperm’s cell membrane, and two of the three proteins form the binding site for the egg protein in zebrafish,” continues Blaha. Graphical abstract showing the evolutionarily conserved trimeric sperm complex composed of Izumo1 (yellow), Spaca6 (lavender), and Tmem81 (red), bound to the egg gatekeeper, that is the protein Bouncer in fish (left, marked in light blue), and Juno in mammals (right, marked in purple). Credit: Deneke et al. 2024 Evolutionary Perspectives on Fertilization The complex on the sperm’s membrane was found to interact with the zebrafish egg’s gatekeeper Bouncer, located on the egg’s surface. Bouncer serves as a lock that only grants access to the egg with the right key, just like its mammalian counterpart Juno. The sperm trimeric complex is evolutionarily conserved across vertebrates, while the interacting egg proteins have changed in different species to mediate the binding of sperm and egg. Andrea Pauli, Andreas Blaha, and Victoria Deneke drove the project that led to the discovery of this fundamental fertilization mechanism. Credit: IMP Conclusion: Significance of the Discovery “The identification of this complex of three proteins is a major step forward,” says Andrea Pauli. “The fact that it was maintained over millions of years of evolution shows just how important this lock-and-key process is. But what is really surprising is that the conserved sperm trimer uses evolutionarily unrelated egg proteins to dock onto the surface of the egg—evolutionary diversity resulting in a universal mechanism, right at the beginning of life!” Reference: “A conserved fertilization complex bridges sperm and egg in vertebrates” by Victoria E. Deneke, Andreas Blaha, Yonggang Lu, Johannes P. Suwita, Jonne M. Draper, Clara S. Phan, Karin Panser, Alexander Schleiffer, Laurine Jacob, Theresa Humer, Karel Stejskal, Gabriela Krssakova, Elisabeth Roitinger, Dominik Handler, Maki Kamoshita, Tyler D.R. Vance, Xinyin Wang, Joachim M. Surm, Yehu Moran, Jeffrey E. Lee, Masahito Ikawa and Andrea Pauli, 17 October 2024, Cell. DOI: 10.1016/j.cell.2024.09.035 RRG455KLJIEVEWWF 茶六燒肉堂整體值得推薦嗎？ 》台中公益路餐廳大賞｜10家特色名店推薦一頭牛日式燒肉必點有哪些？ 》公益路10家人氣餐廳｜台中美食一網打盡一笈壽司節慶時段會不會太難訂位？ 》台中公益路美食攻略｜精選10間超人氣餐廳，一次帶你吃遍熱門口袋名單 |
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