עבודה זו מומנה על ידי תוכנית מדע האדם Frontier מענק RGP0024.

1. תבנית ה-DNA הכנה בתעתיק חוץ גופית <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> הגן של הריבית לשכפל בכל T7 ו / או למשל SP6 האמרגן מבוסס פלסמיד. כדי להשיג RNCs של עניין, C-הסופית של יעד פוליפפטיד הוארך על ידי הוספת התרמה מעצר רצף של SecM FXXXXWIXXXXGIRAGP 7. על מנת להבטיח כי שבר פוליפפטיד מעניין יהיה extrude מתוך המנהרה ריבוזומלי, החלק C-טרמינל של חלבון המטרה צריכה להיות מורחבת על ידי לפחות 30 חומצות אמינו 12-14. מקשר גליצין, סרין גמישה עשיר יכול להיות מוצג בין חלבון לבין רצף מעצר SecM כדי למנוע אילוצים קונפורמציה אפשריים. </li><li style=";text-align:right;direction:rtl"> עבור בתעתיק חוץ גופית, תבנית ה-DNA יש לינארית עם אנזים הגבלה חותך במורד הזרם של ORF. יש צורך לאמת את לינאריזציה מלאה של DNA פלסמיד על ידי הפעלת המוצר העיכול מגבלה על ג&#39;ל אלקטרופורזה agarose. </li><li style=";text-align:right;direction:rtl"> בפלסמה לינאריתid משמש נוספת בתגובה שעתוק במבחנה. ריכוז שונה של DNA התבנית ניתן לבדוק לזהות ריכוז ה-DNA האופטימלי הנדרש ב שעתוק במבחנה. בדרך כלל עם ערכת MEGAscript של Ambion תמלול, תפוקה גבוהה (Ambion / Life Technologies, גרנד איילנד, ניו יורק), ה-DNA 1 מיקרוגרם לינארית מניבה mRNA 40-60 מיקרוגרם. בתעתיק חוץ גופית נעשית בעקבות הוראה של היצרן (Ambion / Life Technologies, גרנד איילנד, ניו יורק) . </li><li style=";text-align:right;direction:rtl"> בעקבות בתעתיק חוץ גופית, mRNA מטוהרים על ידי משקעים ליתיום כלוריד על פי הוראה של היצרן (MEGAscript תמלול העליון Ambion ערכת התשואה Ambion / Life Technologies, גרנד איילנד, ניו יורק). </li><li style=";text-align:right;direction:rtl"> שלמות mRNA מאומת עוד יותר על ידי אלקטרופורזה באמצעות acrylamide או ג&#39;ל agarose. </li></ol> 2. במבחנה תרגום עבור בתרגום חוץ גופית באמצעות 100 RTS א coli ח.י. Kit (5 הממשלה, גאיתרsburg, MD) בצע את הפעולות הבאות: <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> הכן 100 μl ההוראה בתגובה במבחנה תרגום יצרן הבאה. בקצרה, במים nuclease חינם להוסיף 24 חומצות אמינו μl תערובת מינוס מתיונין (1 מ&quot;מ), 10 יחידות של מעכבי Ribonuclease (Invitrogen / Life טכנולוגיות, גרנד איילנד, ניו יורק), 20 μCi של רדיואקטיבי-מתיונין (S [35] Biomedicals מגה פיקסל, סולון, OH), 20 תערובת התגובה μl, 24 חיץ הכינון מחדש μl ו 24 μl של א &#39; lysate coli. </li><li style=";text-align:right;direction:rtl"> דגירה התגובה על 30 מעלות צלזיוס למשך 5 דקות מראש תגובה חמה תרגום. להוסיף 1-2 מיקרוגרם של ה-mRNA לתגובה תרגום דגירה על 30 מעלות צלזיוס במשך 10-15 דקות. </li><li style=";text-align:right;direction:rtl"> לעצור את התגובה על ידי הנחת התגובה התרגום על הקרח. </li></ol> 3. הבידוד של פוליפפטיד ינוקא מ בתגובה תרגום חוץ גופית <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> לבודד RNCs, התגובה התרגום שכבות על גבי שיפוע של 4.5 מ&quot;ל 5-30% סוכרוז ב-pH 20 מ&quot;מ HEPES-KOH 70.5, 15 מ&quot;מ MgCl 2, 100 אצטט mM אשלגן, 1 mM DTT וכן באמצעות centrifuged Beckman Coulter SW55-Ti הרוטור ב 41000 סל&quot;ד, 4 מעלות צלזיוס למשך 2 שעות. </li><li style=";text-align:right;direction:rtl"> לאחר צנטריפוגה, שיפוע סוכרוז הוא מופרדים לבודד אוכלוסיות ריבוזומלי שונים ורשתות המתהווה הכרוכים בכך. ההפרדה מנוטר באמצעות צבע לתכנות ISCO מערכת צפיפות עם הקלטה רציפה ב 254 ננומטר באמצעות גלאי ISCO UA-6 ספיגת. </li><li style=";text-align:right;direction:rtl"> חלק קטן (S) המכילה ריבוזומים ה -70 הם לאסוף ולנתח נוספת בהתאם המטרה של הניסוי. </li></ol> 4. תצפית של חלבון כך נגזר, ריבוזום עם טריס-tricine SDS PAGE כדי לבדוק זאת, אם חלבון ממושכת SecM נשארת מחוברת ה -70 הריבוזום, שברים הדרגתיים נאספו וטופלו באופן הבא: <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> חלבון בשבריר כל אחד זירז ידי הוספת חומצה Trichloroacetic (TCA) לריכוז סופי של 10% ו מודגרות ב 4 ° C overnight. </li><li style=";text-align:right;direction:rtl"> לאחר הדגירה לילה, דגימות היו centrifuged על 14,000 X גרם במשך 15 דקות כדי גלולה חלבון. Supernatant צנטריפוגה הבאה הוסר גלולה נשטף פעמיים עם אצטון תמיסה המכילה: 1 mM Tris-HCl pH 7.6 (04:01). גלולה היה באוויר עוד יותר יבשים מומסים חיץ SDS-PAGE הטעינה. </li><li style=";text-align:right;direction:rtl"> המדגם התייחס נפתרה ונותחו על ידי טריס-tricine SDS-PAGE. </li><li style=";text-align:right;direction:rtl"> לאחר אלקטרופורזה, ג&#39;לים תוקנו, מיובשים באמצעות ואקום ג&#39;ל דייר ו נתון autoradiography. הפצה של פוליפפטידים המתהווה נצפו באמצעות phosphoimaging. </li></ol> 5. נציג תוצאות כאן אנו מציגים ניסוי המתאר את בידודו של באורך מלא שור Gamma-B Crystallin קשור ביציבות אל שנות ה -70 הריבוזום. איור 1 מתאר את השלבים הכרוכים בבידוד של RNCs שור Gamma-B Crystallin. C-הסופית של Crystallin Gamma-B הוארך הכוללת של חומצות אמינו לא 32הו להבטיח באורך מלא מוציא חלבון מתוך המנהרה ריבוזומלי, זה כולל גם את רצף SecM השתהות שהוצב מאוד C-הסופית של היתוך פוליפפטיד. בעקבות בתרגום חוץ גופית, ריבוזומים ה -70 בודדו על ידי צנטריפוגה סוכרוז שיפוע (איור 2.1). על מנת להבטיח כי החלבון נשאר חייב ביציבות אל הריבוזום, בשנות ה -70 המכילים שברים היו נקווה, מאגר desalted, החליפו וכפופים לסיבוב נוסף של צנטריפוגה גרדיאנט סוכרוז (איור 2.2). התוצאה מוצגת באיור 2 עולה בבירור כי SecM ביעילות לגרום למעצר translational של RNCs את Gamma-B Crystallin. <img alt="איור 1" src="/files/ftp_upload/4027/4027fig1.jpg" /> באיור 1. הסבר סכמטי של המעורבים בידוד RNCs. C-הסופית של Crystallin שור Gamma-B הוארך רצף 32 חומצות אמינו. זה המורחבתבטרמינל C-אזורים כולל גם רצף מעצר SecM. Gamma-B Crystallin עם רצף SecM שוכפלה ב pIVEX 2.3 (מבוסס T7) הפלסמיד. שכן שעתוק במבחנה DNA התבנית לינארית על ידי XbaI. תבנית לינארית שימש נוספת של שעתוק במבחנה. T7 בתבנית ה-DNA הוא מוכר על ידי RNA פולימראז T7 כי מעתיק את Gamma-B Crystallin גנים הממוקמים במורד של האמרגן T7. mRNA היה מטוהרים באמצעות ליתיום כלוריד שיטת משקעים. MRNA מטוהרים היה אז בשימוש עבור בתרגום חוץ גופית. הדגירה הבאה, התגובה התרגום שכבות על גבי שיפוע 5-30% סוכרוז centrifuged ב Beckman Coulter SW55-Ti הרוטור ב 41000 סל&quot;ד, 4 מעלות צלזיוס למשך 2 שעות. <spבכיתה = &quot;pdflinebreak&quot;&gt; <img alt="איור 2" src="/files/ftp_upload/4027/4027fig2.jpg" /> איור 2. הבידוד של Crystallin שור Gamma-B RNCs קשור ביציבות אל הריבוזום ה -70. 1 mRNA מיקרוגרם היה מעורב ב 100 התגובה ה μl coli מערכת S30 תמצית כאמור בסעיף 20 לפרוטוקול עם μCi [35 S]-מתיונין מודגרות על 30 מעלות צלזיוס במשך 15 דקות. הדגירה הבאה, התגובה התרגום שכבות על גבי שיפוע 5-30% סוכרוז ב 20 HEPES-KOH mM pH 7.5, 15 מ&quot;מ MgCl 2, אצטט אשלגן 100 מ&quot;מ, 1 mM DTT ו centrifuged ב Beckman Coulter SW55-Ti הרוטור ב 41000 סל&quot;ד, 4 מעלות צלזיוס למשך 2 שעות. לאחר שקיעה מהירות, שיפוע נפרק את הריבוזום Pro Le הושג. הנתונים נרשמו על ידי תוכנית PeakTrak (צפיפות ISCO שיפוע שיפוע מערכת חלוקה). נאספו שברים, החלבון היה TCA זירז והחליט על T 16.5%, 6% C טריס-Tricine PAGE ג&#39;ל 15. ג&#39;ל היה יבש וחשוף עבור autoradiography. החשיפה הבאה ג&#39;ל נסרק באמצעות טייפון 9410 סורק הדמיה. איור 2.1 מראה באורך מלא, Gamma-B Crystallin קיים בשנות ה -70 שברים הריבוזום. לפיכך, רצף SecM השתהות מאפשר בידוד של האורווה Gamma-B RNCs שור Crystallin. הנתונים איור 2.2 עולה בבירור כי את RNCs בודדים הם יציבים מאוד. בניסוי הנוכחי ה -70 שברים לאחר הסיבוב הראשון של צנטריפוגה גרדיאנט סוכרוז היו נקווה ואת סוכרוז הוסר באמצעות Amicon Ultra-4 יחידת מסנן צנטריפוגלי (Millipore), ואחריו מאגר החליפין תמיסה המכילה 20 מ&quot;מ HEPES KOH-pH 7.5, 15 מ&quot;מ MgCl 2, אשלגן 100 mM אצטט, DTT 1 מ&quot;מ. מדגם זה היה נתון עוד יותר לסיבוב נוסף של צנטריפוגה דרך שיפוע 5-30% סוכרוז ו מופרדים. חלק זה טופל וניתח כמו באיור 2.1.

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אין ניגוד עניינים הצהיר.

לקבלת תוצאות לשחזור, איכות ריכוז המרכיבים המשמשים ב שעתוק במבחנה התרגום הן קריטיות. השתמשנו זמינים מסחרית שעתוק במבחנה תמציות תרגום והם נותנים תוצאות יעיל לשחזור, אם מטופל בזהירות. האיכות של ה-mRNA יכול להשפיע על התרגום, ולכן הוא בעל חשיבות עליונה ל?...

<table border="1" style=";text-align:right;direction:rtl"><tbody><tr><td> שם מגיב / Kit </td><td> חברה </td><td> מספר קטלוגי </td></tr><tr><td> MEGAscript T7 ערכת גבוהה תמלול תשואה </td><td> Ambion </td><td> AM1333 </td></tr><tr><td> RTS 100 E.coli ח.י. Kit </td><td> 5 ראש </td><td> 2401100 </td></tr><tr><td> Ribonuclease אינהיביטור </td><td> Invitrogen </td><td> 15518012 </td></tr><tr><td> חוצה [35 S]-Label </td><td> מגה פיקסל Biomedicals </td><td> 0151006 </td></tr><tr><td> Amicon Ultra-4 יחידת מסנן צנטריפוגלי </td><td> Millipore </td><td> UFC801008 </td></tr><tr><td> אחסון זרחן autoradiography </td><td> GE Healthcare </td><td> טייפון 9410 במצב משתנה imager </td></tr><tr><td> שיפוע צפיפות חלוקה מערכות </td><td> Teledyne Isco, Inc </td><td> ISCO צפיפות לתכנות Gradient מערכת </td></tr><tr><td> סוכרוז צבע CENtrifugation </td><td> Beckman Coulter </td><td> אופטימה L-90 K ultracentrifuge preparative </td></tr></tbody></table>

using secm arrest sequence as a tool to isolate ribosome bound polypeptides

מחקר מקיף סיפקה ראיות בשפע טוען כי קיפול חלבונים בתא הוא תהליך שיתוף translational 1-5. עם זאת, המסלול המדויק שרשרת פוליפפטיד כדלקמן במהלך קיפול שיתוף translational להשיג טופס הפונקציונלי הוא עדיין חידה. על מנת להבין את התהליך הזה כדי לקבוע את הקונפורמציה המדויק של שיתוף ביניים של תרגום מתקפלים, חשוב לפתח שיטות המאפשרות בידוד של RNCs שנשאו רשתות המתהווה בגדלים קבועים מראש על מנת לאפשר ניתוח מבנית נוספת שלהם. SecM (צג הפרשת) הוא 170 חומצות אמינו א &#39; coli חלבון המווסת את ביטוי של ATPase במורד הזרם (נהיגה הפרשת) SecA ב operon secM-secA 6. Nakatogawa ו איטו במקור נמצא כי רצף 17 חומצות אמינו ארוכה (150-FSTPVWISQA QGIRA G P-166) באזור C-terminal של החלבון SecM מספיק וצריךכי השתהות של התארכות SecM ב Gly165, ובכך לייצר peptidyl-glycyl-tRNA קשורה ביציבות אל ריבוזומלי P-האתר 7-9. יתרה מכך, נמצא כי 17 זה רצף חומצות האמינו זמן רב ניתן קיבע את הסופית-C של חלבון כמעט בכל באורך מלא ו / או מקוצר ובכך מאפשר ייצור של RNCs שנשאו רשתות המתהווה בגדלים קבועים מראש 7. לכן, כאשר התמזגו או מוכנס לתוך היעד החלבון, רצף SecM מייצר השתהות מעצרו של התארכות שרשרת פוליפפטיד ומייצר RNCs יציבים הן in vivo של א &#39; קולי תאים במבחנה במערכת התא ללא. שיפוע צנטריפוגה סוכרוז הוא מנוצל יותר לבודד RNCs. RNCs את בודדים ניתן לנתח מאפיינים מבניים ותפקודיים של שיתוף ביניים של תרגום מתקפלים. לאחרונה, טכניקה זו שימשה בהצלחה להבנה טובה של המבנה של הריבוזום שרשראות כמה המתהווה קשורות 10,11. כאן אנו מתארים את הבידוד של Crystallin שור Gamma-B RNCs התמזגו כדי SecM ו שנוצר במערכת בתרגום חוץ גופית.

Watch this Scientific Journal Video about Using SecM Arrest Sequence as a Tool to Isolate Ribosome Bound Polypeptides at JoVE.com

Using SecM Arrest Sequence as a Tool to Isolate Ribosome Bound Polypeptides

המתואר כאן טכניקה כיום בשימוש שגרתי לבודד קשורות ביציבות הריבוזום מתחמי הרשת המתהווה (RNCs). שיטה זו מנצלת את הגילוי כי 17 חומצות אמינו ארוכה SecM &quot;מעצר רצף&quot; יכול לעצור את התארכות תרגום פרוקריוטים (<em&gt; א &#39; coli</em&gt;) המערכת, כאשר מוכנס לתוך (או התמזגו למסוף-C) של חלבון כמעט בכל.

באמצעות רצף מעצר SecM ככלי לבודד פוליפפטידים כרוכים הריבוזום

Extensive research has provided ample evidences suggesting that protein folding in the cell is a co-translational process1-5. However, the exact pathway ...

using-secm-arrest-sequence-as-tool-to-isolate-ribosome-bound

Research

JoVE Journal

Biology

12.3K Views.  Cleveland State University. המתואר כאן טכניקה כיום בשימוש שגרתי לבודד קשורות ביציבות הריבוזום מתחמי הרשת המתהווה (RNCs). שיטה זו מנצלת את הגילוי כי 17 חומצות אמינו ארוכה SecM "מעצר רצף" יכול לעצור את התארכות תרגום פרוקריוטים ( א ' coli) המערכת, כאשר מוכנס לתוך (או התמזגו למסוף-C) של חלב?...

Video: Using SecM Arrest Sequence as a Tool to Isolate Ribosome Bound Polypeptides

Microfabricated Post-Array-Detectors (mPADs): an Approach to Isolate Mechanical Forces

In this video, we will present our approach to measure cellular traction forces using a microfabricated array of posts.  Traction forces are generated through myosin-actin interactions and play an important role in our physiology.  During development, they enable cells to move from one location to the next in order to form the early structures of tissue.  Traction forces help in the healing processes.  They are necessary for the proper closure of wounds or the migration and crawling of leukocytes through our body.  These same forces can be detrimental to our health in the case of cancer metastasis or vascular growth towards a tumor.  The most common method by which to study cells in vitro has been to use a glass or polystyrene dish.  However, the rigidity of the substrates makes it impossible to physically measure cell traction forces, and there are relatively few methods to study traction forces.  Our lab has developed a technique to overcome these limitations.  The method is based on a vertical array of flexible cantilevers, the stiffness and size scale of which are such that individual cells spread across many cantilevers and deflect them in the process.  The pillars we use are 3 &mu;m in diameter, 10 &mu;m tall, and are configured in a regular array with 9 &mu;m center-to-center spacing.  But these physical dimensions can be readily varied to accommodate a variety of studies.  We start with a silicon master, but the final posts are made out of silicone rubber called poly (dimethyl siloxane), or PDMS.  We can measure the deflections under a microscope and calculate the magnitude and direction of traction forces required to produce the observed deflections.  We call these substrates microfabricated post-array-detectors, or mPADs.  Here, we will show you how we fabricate and use the mPADs to assess modulations of cellular contractility.

Microfabricated Post-Array-Detectors mPADs: an Approach to Isolate Mechanical Forces

In this video, we demonstrate how to fabricate and utilize microfabricated post array detectors (mPADs) to assess modulations of cellular contractility.

Microfabricated פוסט מערך גלאים (mPADs): גישה לבודד כוחות מכניים

In this video, we will present our approach to measure cellular traction forces using a microfabricated array of posts.  Traction forces are generated ...

Correlative Light and Electron Microscopy (CLEM) as a Tool to Visualize Microinjected Molecules and their Eukaryotic Sub-cellular Targets

The eukaryotic cell relies on complex, highly regulated, and functionally distinct membrane bound compartments that preserve a biochemical polarity necessary for proper cellular function. Understanding how the enzymes, proteins, and cytoskeletal components govern and maintain this biochemical segregation is therefore of paramount importance. The use of fluorescently tagged molecules to localize to and/or perturb subcellular compartments has yielded a wealth of knowledge and advanced our understanding of cellular regulation. Imaging techniques such as fluorescent and confocal microscopy make ascertaining the position of a fluorescently tagged small molecule relatively straightforward, however the resolution of very small structures is limited 1.
On the other hand, electron microscopy has revealed details of subcellular morphology at very high resolution, but its static nature makes it difficult to measure highly dynamic processes with precision 2,3. Thus, the combination of light microscopy with electron microscopy of the same sample, termed Correlative Light and Electron Microscopy (CLEM) 4,5, affords the dual advantages of ultrafast fluorescent imaging with the high-resolution of electron microscopy 6. This powerful technique has been implemented to study many aspects of cell biology 5,7. Since its inception, this procedure has increased our ability to distinguish subcellular architectures and morphologies at high resolution. 
Here, we present a streamlined method for performing rapid microinjection followed by CLEM (Fig. 1). The microinjection CLEM procedure can be used to introduce specific quantities of small molecules and/or proteins directly into the eukaryotic cell cytoplasm and study the effects from millimeter to multi-nanometer resolution (Fig. 2). The technique is based on microinjecting cells grown on laser etched glass gridded coverslips affixed to the bottom of live cell dishes and imaging with both confocal fluorescent and electron microscopy. Localization of the cell(s) of interest is facilitated by the grid pattern, which is easily transferred, along with the cells of interest, to the Epon resin used for immobilization of samples and sectioning prior to electron microscopy analysis (Fig. 3). Overlay of fluorescent and EM images allows the user to determine the subcellular localization as well as any morphological and/or ultrastructural changes induced by the microinjected molecule of interest (Fig. 4). This technique is amenable to time points ranging from &le;5 s up to several hours, depending on the nature of the microinjected sample.

Correlative Light and Electron Microscopy CLEM as a Tool to Visualize Microinjected Molecules and their Eukaryotic Sub-cellular Targets

The CLEM technique has been adapted to analyze ultrastructural morphology of membranes, organelles, and subcellular structures affected by microinjected molecules. This method combines the powerful techniques of micromanipulation/microinjection, confocal fluorescent microscopy, and electron microscopy to allow millimeter to multi-nanometer resolution. This technique is amenable to a wide variety of applications.

אור גומל ומיקרוסקופי אלקטרונים (קלם) ככלי למדמיינים מולקולות Microinjected והיעדים האיקריוטים תת סלולריים


The eukaryotic cell relies on complex, highly regulated, and functionally distinct membrane bound compartments that preserve a biochemical polarity ...

Electroantennographic Bioassay as a Screening Tool for Host Plant Volatiles

Plant volatiles play an important role in plant-insect interactions. Herbivorous insects use plant volatiles, known as kairomones, to locate their host plant.1,2 When a host plant is an important agronomic commodity feeding damage by insect pests can inflict serious economic losses to growers. Accordingly, kairomones can be used as attractants to lure or confuse these insects and, thus, offer an environmentally friendly alternative to pesticides for insect control.3 Unfortunately, plants can emit a vast number volatiles with varying compositions and ratios of emissions dependent upon the phenology of the commodity or the time of day. This makes identification of biologically active components or blends of volatile components an arduous process. To help identify the bioactive components of host plant volatile emissions we employ the laboratory-based screening bioassay electroantennography (EAG). EAG is an effective tool to evaluate and record electrophysiologically the olfactory responses of an insect via their antennal receptors. The EAG screening process can help reduce the number of volatiles tested to identify promising bioactive components. However, EAG bioassays only provide information about activation of receptors. It does not provide information about the type of insect behavior the compound elicits; which could be as an attractant, repellent or other type of behavioral response. Volatiles eliciting a significant response by EAG, relative to an appropriate positive control, are typically taken on to further testing of behavioral responses of the insect pest. The experimental design presented will detail the methodology employed to screen almond-based host plant volatiles4,5 by measurement of the electrophysiological antennal responses of an adult insect pest navel orangeworm (Amyelois transitella) to single components and simple blends of components via EAG bioassay. The method utilizes two excised antennae placed across a "fork" electrode holder. The protocol demonstrated here presents a rapid, high-throughput standardized method for screening volatiles. Each volatile is at a set, constant amount as to standardize the stimulus level and thus allow antennal responses to be indicative of the relative chemoreceptivity. The negative control helps eliminate the electrophysiological response to both residual solvent and mechanical force of the puff. The positive control (in this instance acetophenone) is a single compound that has elicited a consistent response from male and female navel orangeworm (NOW) moth. An additional semiochemical standard that provides consistent response and is used for bioassay studies with the male NOW moth is (Z,Z)-11,13-hexdecadienal, an aldehyde component from the female-produced sex pheromone.6-8

A method to rapidly screen host plant volatiles by measurement of the electrophysiological response of adult navel orangeworm (Amyelois transitella) antennae to single components and blends via electroantennographic analysis is demonstrated.

המבדק Electroantennographic ככלי מיון עבור נדיפים צמחים מארח

Plant volatiles play an important role in plant-insect interactions. Herbivorous insects use plant volatiles, known as kairomones, to locate their host ...

Isolation of Ribosome Bound Nascent Polypeptides in vitro to Identify Translational Pause Sites Along mRNA

The rate of translational elongation is non-uniform. mRNA secondary structure, codon usage and mRNA associated proteins may alter ribosome movement on the messagefor review see 1. However, it's now widely accepted that synonymous codon usage is the primary cause of non-uniform translational elongation rates1. Synonymous codons are not used with identical frequency. A bias exists in the use of synonymous codons with some codons used more frequently than others2. Codon bias is organism as well as tissue specific2,3. Moreover, frequency of codon usage is directly proportional to the concentrations of cognate tRNAs4. Thus, a frequently used codon will have higher multitude of corresponding tRNAs, which further implies that a frequent codon will be translated faster than an infrequent one. Thus, regions on mRNA enriched in rare codons (potential pause sites) will as a rule slow down ribosome movement on the message and cause accumulation of nascent peptides of the respective sizes5-8. These pause sites can have functional impact on the protein expression, mRNA stability and protein foldingfor review see 9. Indeed, it was shown that alleviation of such pause sites can alter ribosome movement on mRNA and subsequently may affect the efficiency of co-translational (in vivo) protein folding1,7,10,11. To understand the process of protein folding in vivo, in the cell, that is ultimately coupled to the process of protein synthesis it is essential to gain comprehensive insights into the impact of codon usage/tRNA content on the movement of ribosomes along mRNA during translational elongation.
Here we describe a simple technique that can be used to locate major translation pause sites for a given mRNA translated in various cell-free systems6-8. This procedure is based on isolation of nascent polypeptides accumulating on ribosomes during in vitro translation of a target mRNA. The rationale is that at low-frequency codons, the increase in the residence time of the ribosomes results in increased amounts of nascent peptides of the corresponding sizes. In vitro transcribed mRNA is used for in vitro translational reactions in the presence of radioactively labeled amino acids to allow the detection of the nascent chains. In order to isolate ribosome bound nascent polypeptide complexes the translation reaction is layered on top of 30% glycerol solution followed by centrifugation. Nascent polypeptides in polysomal pellet are further treated with ribonuclease A and resolved by SDS PAGE. This technique can be potentially used for any protein and allows analysis of ribosome movement along mRNA and the detection of the major pause sites. Additionally, this protocol can be adapted to study factors and conditions that can alter ribosome movement and thus potentially can also alter the function/conformation of the protein.

Isolation of Ribosome Bound Nascent Polypeptides in vitro to Identify Translational Pause Sites Along mRNA

A technique to identify translational pause sites on mRNA is described. This procedure is based on isolation of nascent polypeptides accumulating on ribosomes during in vitro translation of a target mRNA, followed by the size analysis of the nascent chains using a denaturing gel electrophoresis.

הבידוד של הריבוזום פוליפפטידים המתהווה כרוכים<em&gt; במבחנה</em&gt; כדי לזהות אתרים השהה של תרגום לאורך ה-mRNA

The rate of translational elongation is non-uniform. mRNA secondary structure, codon usage and mRNA associated proteins may alter ribosome movement on the ...

Using Caenorhabditis elegans as a Model System to Study Protein Homeostasis in a Multicellular Organism

The folding and assembly of proteins is essential for protein function, the long-term health of the cell, and longevity of the organism. Historically, the function and regulation of protein folding was studied in vitro, in isolated tissue culture cells and in unicellular organisms. Recent studies have uncovered links between protein homeostasis (proteostasis), metabolism, development, aging, and temperature-sensing. These findings have led to the development of new tools for monitoring protein folding in the model metazoan organism Caenorhabditis elegans. In our laboratory, we combine behavioral assays, imaging and biochemical approaches using temperature-sensitive or naturally occurring metastable proteins as sensors of the folding environment to monitor protein misfolding. Behavioral assays that are associated with the misfolding of a specific protein provide a simple and powerful readout for protein folding, allowing for the fast screening of genes and conditions that modulate folding. Likewise, such misfolding can be associated with protein mislocalization in the cell. Monitoring protein localization can, therefore, highlight changes in cellular folding capacity occurring in different tissues, at various stages of development and in the face of changing conditions. Finally, using biochemical tools ex vivo, we can directly monitor protein stability and conformation. Thus, by combining behavioral assays, imaging and biochemical techniques, we are able to monitor protein misfolding at the resolution of the organism, the cell, and the protein, respectively.

Using Caenorhabditis elegans as a Model System to Study Protein Homeostasis in a Multicellular Organism

To study the relationship between protein homeostasis, stress and aging, we monitored changes in protein folding by following protein dysfunction, protein localization in the cell and protein stability at the organismal, cellular and protein levels, using the genetically tractable metazoan Caenorhabditis elegans as a model system.

The folding and assembly of proteins is essential for protein function, the long-term health of the cell, and longevity of the organism. Historically, the ...

Xenopus laevis as a Model to Identify Translation Impairment

Protein synthesis is a fundamental process to gene expression impacting diverse biological processes notably adaptation to environmental conditions. The initiation step, which involves the assembly of the ribosomal subunits at the mRNA initiation codon, involved initiation factor including eIF4G1. Defects in this rate limiting step of translation are linked to diverse disorders. To study the potential consequences of such deregulations, Xenopus laevis oocytes constitute an attractive model with high degrees of conservation of essential cellular and molecular mechanisms with human. In addition, during meiotic maturation, oocytes are transcriptionally repressed and all necessary proteins are translated from preexisting, maternally derived mRNAs. This inexpensive model enables exogenous mRNA to become perfectly integrated with an effective translation. Here is described a protocol for assessing translation with a factor of interest (here eIF4G1) using stored maternal mRNA that are the first to be polyadenylated and translated during oocyte maturation as a physiological readout. At first, mRNA synthetized by in vitro transcription of plasmids of interest (here eIF4G1) are injected in oocytes and kinetics of oocyte maturation by Germinal Vesicle Breakdown detection is determined. The studied maternal mRNA target is the serine/threonine-protein-kinase mos. Its polyadenylation and its subsequent translation are investigated together with the expression and phosphorylation of proteins of the mos signaling cascade involved in oocyte maturation. Variations of the current protocol to put forward translational defects are also proposed to emphasize its general applicability. In light of emerging evidence that aberrant protein synthesis may be involved in the pathogenesis of neurological disorders, such a model provides the opportunity to easily assess this impairment and identify new targets.

Xenopus laevis as a Model to Identify Translation Impairment

Protein synthesis control occurs mainly at the translation initiation step, deficiencies in which are linked to diverse disorders. To better understand their etiology, we described here a protocol using Xenopus laevis oocytes assessing the translation of mos transcript in the presence of a mutant of translation initiation factor eIF4G1.

Xenopus laevis כמודל לזיהוי תרגום ירידת ערך

Protein synthesis is a fundamental process to gene expression impacting diverse biological processes notably adaptation to environmental conditions. The ...

Examination of Proteins Bound to Nascent DNA in Mammalian Cells Using  BrdU-ChIP-Slot-Western Technique

Histone deacetylases 1 and 2 (HDAC1,2) localize to the sites of DNA replication. In the previous study, using a selective inhibitor and a genetic knockdown system, we showed novel functions for HDAC1,2 in replication fork progression and nascent chromatin maintenance in mammalian cells. Additionally, we used a BrdU-ChIP-Slot-Western technique that combines chromatin immunoprecipitation (ChIP) of bromo-deoxyuridine (BrdU)-labeled DNA with slot blot and Western analyses to quantitatively measure proteins or histone modification associated with nascent DNA.
Actively dividing cells were treated with HDAC1,2 selective inhibitor or transfected with siRNAs against Hdac1 and Hdac2 and then newly synthesized DNA was labeled with the thymidine analog bromodeoxyuridine (BrdU). The BrdU labeling was done at a time point when there was no significant cell cycle arrest or apoptosis due to the loss of HDAC1,2 functions. Following labeling of cells with BrdU, chromatin immunoprecipitation (ChIP) of histone acetylation marks or the chromatin-remodeler was performed with specific antibodies. BrdU-labeled input DNA and the immunoprecipitated (or ChIPed) DNA was then spotted onto a membrane using the slot blot technique and immobilized using UV. The amount of nascent DNA in each slot was then quantitatively assessed using Western analysis with an anti-BrdU antibody. The effect of loss of HDAC1,2 functions on the levels of newly synthesized DNA-associated histone acetylation marks and chromatin remodeler was then determined by normalizing the BrdU-ChIP signal obtained from the treated samples to the control samples.

In this protocol, we describe a novel BrdU-ChIP-Slot-Western technique to examine proteins and histone modifications associated with newly synthesized or nascent DNA.

בדיקה של החלבונים Bound לינוקא DNA בתאי יונקים באמצעות טכניקת BrdU-שבב חריץ-מערבי

Histone deacetylases 1 and 2 (HDAC1,2) localize to the sites of DNA replication. In the previous study, using a selective inhibitor and a genetic ...

Laser-assisted Microdissection (LAM) as a Tool for Transcriptional Profiling of Individual Cell Types

The understanding of developmental processes at the molecular level requires insights into transcriptional regulation, and thus the transcriptome, at the level of individual cell types. While the methods described here are generally applicable to a wide range of species and cell types, our research focuses on plant reproduction. Plant cultivation and seed production is of crucial importance for human and animal nutrition. A detailed understanding of the regulatory networks that govern the formation of the reproductive lineage (germline) and ultimately of seeds is a precondition for the targeted manipulation of plant reproduction. In particular, the engineering of apomixis (asexual reproduction through seeds) into crop plants promises great improvements, as it leads to the formation of clonal seeds that are genetically identical to the mother plant. Consequently, the cell types of the female germline are of major importance for the understanding and engineering of apomixis. However, as the corresponding cells are deeply embedded within the floral tissues, they are very difficult to access for experimental analyses, including cell-type specific transcriptomics. To overcome this limitation, sections of individual cells can be isolated by laser-assisted microdissection (LAM). While LAM in combination with transcriptional profiling allows the identification of genes and pathways active in any cell type with high specificity, establishing a suitable protocol can be challenging. Specifically, the quality of RNA obtained after LAM can be compromised, especially when small, single cells are targeted. To circumvent this problem, we have established a workflow for LAM that reproducibly results in high RNA quality that is well suitable for transcriptomics, as exemplified here by the isolation of cells of the female germline in apomictic Boechera. In this protocol, procedures are described for tissue preparation and LAM, also with regard to RNA extraction and quality control.

Laser-assisted Microdissection LAM as a Tool for Transcriptional Profiling of Individual Cell Types

Here we present a protocol for laser-assisted microdissection of specific plant cell types for transcriptional profiling. While the protocol is suitable for different species and cell types, the focus is on highly inaccessible cells of the female germline important for sexual and apomictic reproduction in the crucifer genus Boechera.

Microdissection לייזר בסיוע (LAM) ככלי פרופיל תעתיק של סוגי תאים בודדים

The understanding of developmental processes at the molecular level requires insights into transcriptional regulation, and thus the transcriptome, at the ...

Magnetic-Activated Cell Sorting Strategies to Isolate and Purify Synovial Fluid-Derived Mesenchymal Stem Cells from a Rabbit Model

Mesenchymal stem cells (MSCs) are the main cell source for cell-based therapy. MSCs from articular cavity synovial fluid could potentially be used for cartilage tissue engineering. MSCs from synovial fluid (SF-MSCs) have been considered promising candidates for articular regeneration, and their potential therapeutic benefit has made them an important research topic of late. SF-MSCs from the knee cavity of the New Zealand white rabbit can be employed as an optimized translational model to assess human regenerative medicine. By means of CD90-based magnetic activated cell sorting (MACS) technologies, this protocol successfully obtains rabbit SF-MSCs (rbSF-MSCs) from this rabbit model and further fully demonstrates the MSC phenotype of these cells by inducing them to differentiate to osteoblasts, adipocytes, and chondrocytes. Therefore, this approach can be applied in cell biology research and tissue engineering using simple equipment and procedures.

This article presents a simple and economic protocol for the straightforward isolation and purification of mesenchymal stem cells from New Zealand white rabbit synovial fluid.

מגנטי תא לפעיל על-מיון אסטרטגיות כדי לבודד ולטהר Synovial נגזר הנוזלים בתאי גזע Mesenchymal ממודל ארנב

Mesenchymal stem cells (MSCs) are the main cell source for cell-based therapy. MSCs from articular cavity synovial fluid could potentially be used for ...

A High Output Method to Isolate Cerebral Pericytes from Mouse

In recent years, cerebral pericytes have become the focus of extensive research in vascular biology and pathology. The importance of pericytes in blood brain barrier formation and physiology is now demonstrated but its molecular basis remains largely unknown. As the pathophysiological role of cerebral pericytes in neurological disorders is intriguing and of great importance, the in vitro models are not only sufficiently appropriate but also able to incorporate different techniques for these studies. Several methods have been proposed as in vitro models for the extraction of cerebral pericytes, although an antibiotic-free protocol with high output is desirable. Most importantly, a method that has increased output per extraction reduces the usage of more animals.
Here, we propose a simple and efficient method for extracting cerebral pericytes with sufficiently high output. The mouse brain tissue homogenate is mixed with a BSA-dextran solution for the separation of the tissue debris and microvascular pellet. We propose a three-step separation followed by filtration to obtain a microvessel rich filtrate. With this method, the quantity of microvascular fragments obtained from 10 mice is sufficient to seed 9 wells (9.6 cm2 each) of a 6-well plate. Most interestingly with this protocol, the user can obtain 27 pericyte rich wells (9.6 cm2 each) in passage 2. The purity of the pericyte cultures are confirmed with the expression of classical pericyte markers: NG2, PDGFR-&#946; and CD146. This method demonstrates an efficient and feasible in vitro tool for physiological and pathophysiological studies on pericytes.

We present a protocol for the extraction of murine cerebral pericytes. Based on an antibiotic-free enrichment oriented pericyte extraction, this protocol is a valuable tool for in vitro studies providing high purity and high yield, thus decreasing the number of experimental animals used.

שיטת פלט גבוהה כדי לבודד קרום הלב של מוחין מהעכבר

In recent years, cerebral pericytes have become the focus of extensive research in vascular biology and pathology. The importance of pericytes in blood ...