Metagenomi Presents Compact SMART Editing Platform at AIChE 7th International Conference on CRISPR Technologies
Metagenomi Presents Compact SMART Editing Platform at AIChE 7th International Conference on CRISPR Technologies
Poster presentation highlights SMART adenine base editors (ABEs)
small enough to be packaged into a single adeno-associated virus (AAV)
海報展示突出了SMARt腺嘌呤鹼基編輯器(ABEs)
足夠小,可以打包成單一腺相關病毒(AAV)
Data demonstrate compact SMART system optimizations allowing for
therapeutically-relevant genome editing
數據表明,緊湊的SMARt系統優化可以實現
與治療相關的基因編輯
EMERYVILLE, Calif., Oct. 14, 2024 (GLOBE NEWSWIRE) -- Metagenomi, Inc. (Nasdaq: MGX), a precision genetic medicines company committed to developing curative therapeutics for patients using its proprietary gene editing toolbox, today presented a poster titled "Engineering of compact and efficient adenine base editors from metagenomic derived systems" at the American Institute of Chemical Engineers (AIChE) 7th International Conference on CRISPR Technologies in San Diego, CA.
加利福尼亞州埃默裏維爾,2024年10月14日(環球新聞社) —Metagenomi,Inc.(納斯達克:MGX),一家致力於利用其專有基因編輯工具箱爲患者開發治癒性治療方案的精準遺傳藥品公司,今天在美國化學工程師學會(AIChE)第七屆CRISPR技術國際會議上,以「從基因組學派生系統工程緊湊高效腺嘌呤鹼基編輯器」爲題展示了一份海報,該會議在加利福尼亞聖地亞哥舉行。
"We are thrilled to share the progress we've made with our compact SMART systems," said Chris Brown, PhD and Head of Discovery at Metagenomi. "Our update highlights the improved efficiency of our SMART platform across multiple targets and cell types. We demonstrated that our SMART nucleases can be engineered into functional base editors within the packaging limits of standard AAV. We believe the improved editing efficiency of these SMART systems will enable pursuit of neuromuscular targets, either on our own or in partnerships."
「我們很高興分享我們在Compact SMARt系統方面取得的進展,」 Metagenomi的發現主任Chris Brown博士表示。「我們的更新突出了我們的SMARt平台在多個靶標和細胞類型上的改進效率。我們證明了我們的SMARt核酸酶可以被工程化爲標準AAV的包裝限制範圍內的功能性鹼基編輯器。我們相信這些SMARt系統的改進編輯效率將使我們能夠追求神經肌肉靶標,無論是自主開展還是與合作伙伴合作。」
Metagenomi's SMART platform potentially addresses a key challenge of in vivo gene editing: efficient delivery of gene editing components to tissues beyond the liver. Currently, AAV is an established approach for delivery to extrahepatic tissues, which is necessary for treating neuromuscular diseases such as Duchenne muscular dystrophy (DMD), familial amyotrophic lateral sclerosis (ALS), and Charcot-Marie-Tooth disease type 1A (CMT1A). Traditional gene editing tools such as SpCas9 exceed the cargo capacity of standard AAV vectors, potentially necessitating the need for dual AAV systems, which may reduce overall editing efficiency, increase required dosages, and complicate the manufacturing process. Metagenomi's SMART genome editing systems are small enough to be packaged into standard AAV vectors, even when additional effector domains are included for base editing, potentially enabling a differentiated therapeutic approach.
Metagenomi的SMARt平台可能解決體內基因編輯的一個關鍵挑戰:將基因編輯元件高效輸送至肝臟以外的組織。目前,AAV是輸送至肝臟以外組織的一種成熟方法,這對治療神經肌肉疾病如杜興氏肌萎縮症(DMD)、家族性肌萎縮側索硬化(ALS)和查爾科特-馬裏-托特病1A型(CMT1A)至關重要。傳統的基因編輯工具如SpCas9超出了標準AAV載體的載荷容量,可能需要雙AAV系統,這可能降低整體編輯效率,增加所需劑量,並複雜化製造過程。Metagenomi的SMARt基因組編輯系統足夠小,可以被打包進標準AAV載體,即使在進行鹼基編輯時包括額外的效應器結構域,可能實現不同iated的治療方法。
Metagenomi has taken a multi-pronged approach to optimizing the SMART platform since its initial discovery (Aliaga Goltsman, Daniela S., et al. "Compact..." Nature Communications, vol. 13, no. 1), including structure-guided engineering enabled through collaboration with Professor David Taylor and his lab at UT Austin (Ocampo, Rodrigo Fregoso, et al. "DNA..." bioRxiv). In addition, Metagenomi has applied advanced artificial intelligence (AI) tools trained on natural SMART enzymes, which was presented at the Cold Spring Harbor Laboratory (CSHL) CRISPR Frontiers conference earlier this year. The AI-driven approach underscores the importance of leveraging multiple cutting-edge techniques to advance next-generation gene editing systems.
自首次發現以來,Metagenomi採取了多管齊下的方法來優化SMARt平台(Aliaga Goltsman,Daniela S.等人。“《...》自然通訊,第13卷,第1號),其中包括通過與Ut Austin的David Taylor教授及其實驗室合作實現的結構引導工程(Ocampo,Rodrigo Fregoso等人。“緊湊型…《自然通訊》第13卷,第1號),包括結構引導工程,通過與Ut Austin的David Taylor教授及其實驗室合作實現DNA..." bioRxiv)。此外,Metagenomi已經應用了在今年早些時候在Cold Spring Harbor 實驗室(CSHL) 的CRISPR前沿會議上展示過的基於自然SMARt酶訓練的先進人工智能(AI)工具。這種基於AI驅動的方法強調了利用多種尖端技術推進下一代基因編輯系統的重要性。
About Metagenomi
Metagenomi is a precision genetic medicines company committed to developing curative therapeutics for patients using its proprietary, comprehensive metagenomics-derived toolbox. Metagenomi is harnessing the power of metagenomics, the study of genetic material recovered from the natural environment, to unlock four billion years of microbial evolution to discover and develop a suite of novel editing tools capable of correcting any type of genetic mutation found anywhere in the genome. Its comprehensive genome editing toolbox includes programmable nucleases, base editors, and RNA and DNA-mediated integration systems (including prime editing systems and clustered regularly interspaced short palindromic repeat associated transposases). Metagenomi believes its diverse and modular toolbox positions the company to access the entire genome and select the optimal tool to unlock the full potential of genome editing for patients. For more information, please visit https://metagenomi.co.
關於Metagenomi公司:Metagenomi公司是一家精準基因醫藥公司,致力於研發治癒患者的治療藥物,採用其專有的綜合代謝組基因組學。 Metagenomi利用代謝組學的力量(即從自然環境中恢復的基因材料的研究)來解鎖40億年的微生物進化,發現和開發一套新穎的編輯工具,能夠糾正基因組中發現的任何類型的基因突變。其全面的基因組編輯工具箱包括可編程核酸酶、鹼基編輯器和RNA和DNA介導的整合系統(包括主編輯系統和成簇規律間隔短迴文重複相關轉座酶)。Metagenomi認爲,其多樣化且模塊化的工具箱讓公司能夠接觸到整個基因組,並選擇最佳工具來解鎖基因組編輯的全部潛力,爲患者帶來更多療法。請訪問 https://metagenomi.co 獲取更多信息。
Metagenomi是一家致力於利用其獨有的全面母體基因組學工具箱爲患者開發治癒療法的精準遺傳醫學公司。Metagenomi正在利用母體基因組學的力量,即從自然環境中恢復的遺傳物質的研究,解鎖40億年的微生物進化,以發現和開發一系列能夠糾正基因組中任何類型的基因突變的新型編輯工具。其全面的基因編輯工具箱包括可編程核酸酶、鹼基編輯酶、RNA和DNA介導的整合系統(包括主編輯系統和聚簇規律間隔短迴文重複相關的轉座酶)。Metagenomi相信其多樣化和模塊化的工具箱使其具備訪問整個基因組並選擇最佳工具以釋放基因組編輯對患者的全部潛力的能力。欲了解更多信息,請訪問網址https://metagenomi.co。
Cautionary Note Regarding Forward‐Looking Statements
This press release contains "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, each as amended. Such statements, which are often indicated by terms such as "anticipate," "believe," "could," "estimate," "expect," "goal," "intend," "look forward to," "may," "plan," "potential," "predict," "project," "should," "will," "would" and similar expressions, include, but are not limited to, any statements relating to our growth strategy and product development programs, including the timing of and our ability to conduct IND-enabling studies, make regulatory filings such as INDs, statements concerning the potential of therapies and product candidates, statements concerning the timing of data presentations and publications, and any other statements that are not historical facts. Forward looking statements are based on management's current expectations and are subject to risks and uncertainties that could negatively affect our business, operating results, financial condition, and stock value. Factors that could cause actual results to differ materially from those currently anticipated include: risks relating to our growth strategy; our ability to obtain, perform under, and maintain financing and strategic agreements and relationships; risks relating to the results of research and development activities; risks relating to the timing of starting and completing clinical trials; uncertainties relating to preclinical and clinical testing; our dependence on third party suppliers; our ability to attract, integrate and retain key personnel; the early stage of products under development; our need for substantial additional funds; government regulation; patent and intellectual property matters; competition; as well as other risks described in "Risk Factors," in our most recent Form 10-K and our most recent 10-Qs on file with the Securities and Exchange Commission. We expressly disclaim any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in our expectations or any changes in events, conditions or circumstances on which any such statement is based, except as required by law, and we claim the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995.
關於前瞻性聲明的注意事項:本新聞稿包含「前瞻性聲明」,其意義爲《1933年證券法》第27A條和《1934年證券交易法》第21E條,各自經過修訂。這些在管理層看到的聲明通常會用「主張」、「信仰」、「可以」、「估計」、「期待」、「目標」、「打算」、「期待」、「可以」、「計劃」、「潛在」、「預測」、「項目」、「應該」、「意願」等類似表達,包括但不限於我們的增長策略和產品開發計劃以及任何陳述都不屬於歷史事實。前瞻性聲明基於管理層當前的期望並面臨可能對我們的業務、營運業績、財務狀況和股票價值產生負面影響的風險和不確定性。可能導致實際結果與目前預期存在明顯差異的因素包括:與我們的增長策略有關的風險;我們獲取、執行和維持融資和戰略協議及關係的能力和風險;與研發活動成果有關的風險;與啓動和完成臨床試驗的時間有關的風險;與臨床前和臨床測試不確定性有關的風險;我們對第三方供應商的依賴;我們吸引、整合和留住關鍵人員的能力;研發階段的產品早期和巨額需要資金;政府監管;專利和知識產權問題;競爭;以及其他在我們最新的10-K表和我們最新的10-Q表中「風險因素」描述的風險,以及我們與證券交易委員會(SEC)進行的後續提交。我們明確否認任何義務或承諾,公開發布任何更新或修訂此處包含的任何前瞻性聲明,以反映我們期望的任何變化或任何基於任何此類聲明所基於的事件、條件或環境的變化,除非法律另有規定,並聲明受1995年私人證券訴訟改革法案包含的保護措施的保護。
本新聞稿包含根據《證券法》第27A條和《證券交易法》第21E條進行修正的「前瞻性陳述」。此類陳述通常以「預計」,「相信」,「可能」,「估計」,「期望」,「目標」,「打算」,「期待」,「可能」,「計劃」,「潛力」,「預測」,「項目」,「應該」,「將」和類似表達方式表示,包括但不限於與我們的增長策略和產品開發計劃相關的任何陳述,包括進行IND啓動研究的時間和能力,進行例如IND的監管申報的時間,與療法和產品候選者潛力相關的陳述,有關數據展示和發表時間的陳述,以及其他不屬於歷史事實的陳述。前瞻性陳述是基於管理層的當前期望,並受到可能對我們的業務,運營結果,財務狀況和股票價值產生負面影響的風險和不確定性的制約。目前預計可能導致實際結果與目前預期不符的因素包括:與增長策略有關的風險; 我們獲得,執行和維持融資和戰略協議和關係的能力風險; 與研究和開發活動的結果有關的風險; 與啓動和完成臨床試驗的時間有關的不確定性; 與臨床前和臨床測試有關的不確定性; 我們對第三方供應商的依賴性; 我們吸引,整合和留住關鍵人員的能力; 產品開發處於早期階段; 我們需要大量額外資金; 政府監管; 專利和知識產權事項; 競爭; 以及其他在提交給美國證券交易委員會的最新10-K和最新10-Q文件中描述的風險。我們明確聲明不承擔或承擔任何義務,以向公衆發佈此處所包含的任何前瞻性陳述的任何更新或修訂,以反映我們的期望變化或任何事件,條件或原因的變化,除非法律規定,我們在1995年刑事訴訟改革法中聲明對前瞻性陳述的安全港進行保護。
Investor Contact:
Simon Harnest - CIO, SVP Investor Relations
simon@metagenomi.co
投資者聯繫人:
Simon Harnest - 首席投資官,高級副總裁投資者關係
simon@metagenomi.co
simon@metagenomi.co
Media Contact:
Ashlye Hodge - Communications Manager
ashlye@metagenomi.co
媒體聯繫人:
Ashlye Hodge - 通信-半導體經理
ashlye@metagenomi.co
譯文內容由第三人軟體翻譯。