morange-nano recruitment to disilid functionalized giant unilamellar vesicles (guvs) for generating protein patterns

דפוס חלבון הפיך מבוקר אור על קרומי שומנים

The formation of protein patterns on cell membranes within subcellular regions gives rise to numerous biological processes, including migration, division, and localized cell-to-cell communication1,2. These protein patterns are regulated in space and time, and are highly dynamic. Replicating such protein patterns in synthetic cells is essential for mimicking cellular processes that arise from them and for gaining a better understanding of how such regulation works at a molecular level. Analogous to what is observed for membranes in living cells, methods for generating protein patterns on artificial membranes must capture their dynamics and provide precise spatiotemporal control.
Among various stimuli, light stands out for providing the highest spatiotemporal control and several additional advantages3. Through regulation with light, it is straightforward to illuminate a desired area at any desired time with unmatched precision. In addition, light provides high tunability as both the light intensity and the pulse durations can be adjusted. Furthermore, visible light is harmless to biomolecules, including proteins, and it is possible to even address multiple functionalities with different wavelengths. Hence, light-responsive approaches based on visible light emerge as promising avenues for the controlled and biorthogonal regulation of protein patterns in space and time4,5,6. Utilizing photoswitchable protein pairs from optogenetics, acting as light-inducible dimerizers, provides a straightforward method for recruiting&#160;specific proteins to membranes. In particular, protein patterns have successfully been formed on artificial membranes using the blue light-triggered interaction between iLID (improved light-inducible dimer, based on the photoswitchable LOV2 domain from&#160;Avena sativa) and Nano (wild-type SspB)7,8, the blue light-inducible SpyTag system (BLISS)9, the green light-responsive&#160;protein tetramer CarH10 and the red light-inducible interaction between PhyB and PIF611.
It has been demonstrated that the photoswitchable interaction between iLID&#160;and Nano5 can be used to photo-pattern proteins on model membranes using blue light7. The iLID/Nano interaction is reversible in the dark, highly specific, and operates under physiological conditions. Anchoring iLID onto lipid membrane models, such as giant unilamellar vesicles (GUVs) or supported lipid bilayers (SLBs), enables light-regulated recruitment of Nano to these membranes, which is reversible in the dark. Notably, we observed that introducing a disordered domain to the N-terminus of iLID (resulting in a protein named disiLID) as a tether to a model lipid membrane enhances Nano recruitment efficiency and reversion dynamics8.
By employing the disiLID/Nano interaction, we have developed a method for generating high contrast patterns of Nano-fused proteins of interest (POI) on SLBs and the external membranes of GUVs. This method allows for the creation of protein patterns with remarkable spatial and temporal resolution and high reversibility within minutes. The detailed protocol outlines the process for locally recruiting proteins onto artificial membranes. Specifically, this is achieved by immobilizing a biotinylated version of disiLID on SLBs and GUVs through the biotin-streptavidin (SAv) interaction. Subsequently, fluorescently labeled Nano (mOrange-Nano) is recruited to these disiLID functionalized membranes under blue light illumination. Our experimental protocol offers a straightforward and adaptable approach for achieving localized protein recruitment to membranes. Importantly, this methodology is not confined to the reported SLB and GUV interfaces or mOrange-Nano; it can be extended to other disiLID-functionalized materials and proteins fused to Nano.

מחבר זרקור: צילום גיוס חלבונים הניתנים להחלפה לדפוסים הפיכים במערכות תאיות מלאכותיות

תבניות דינמיות של חלבונים המושרים על ידי אור בממברנות המודל

In our work, we aim to reproduce cellular processes in artificial cell-like models that require the precise localization of proteins in a given spot at a certain time. Here, as an example, we demonstrate the formation of dynamic protein patterns on model lipid membranes with high precision and high spatial temporal control using photoswitchable proteins and visible light. One of the current experimental challenge consists of reproducing dynamic protein patterns on model lipid membranes.Here, we need to manipulate these protein patterns fast and reversably with high precision in a biocompatible and non-invasive way. We use photoswitchable proteins to recruit and pattern proteins of interest on supported lipid bilayers and giant unilamellar vesicles. We achieve rapid and localized protein recruitment, and the protein patterning is fully reversible in the dark and can be repeated multiple times.In our protocol, we employ visible light to form protein patterns. Light is an attractive triggers to control interactions with high spatiotemporal resolution and tunability. Light is also not invasive and doesn't damage biomolecules.

mOrange-Nano גיוס ל-disiLID Functional Giant Unilamellar Vesicles (GUVs) ליצירת תבניות חלבונים 

כדי להתחיל, קח את הצינור של GUV שזה עתה נקטף. מוסיפים תמיסת סטרפטווידין, ומניחים לה לשבת במשך 30 דקות בטמפרטורת החדר. לאחר מכן הוסף מיקרומולר אחד של b-disiLID לתמיסת ה- GUV.כסו את הדגימה ברדיד אלומיניום ושמרו אותה בחושך. טפל בתא תחתון מזכוכית 18 באר מיקרו מגלשה עם 150 מיקרוליטר של תמיסת BSA למשך 10 דקות. לאחר מכן להסיר את הפתרון BSA ולשטוף את הבארות שלוש פעמים עם 150 מיקרוליטר מים.לאחר מכן, להוסיף 145 מיקרוליטר של 200 mOrange-nano ננו בחיץ לבאר. הוסף חמישה מיקרוליטרים של GUV מעוטר b-disiLID לתמיסה. מכסים את הדגימה ברדיד אלומיניום וממתינים כ-15 דקות עד שהבועיות מתיישבות.לאחר מכן, הניחו את מגלשת המיקרו מתחת למיקרוסקופ הקונפוקלי. הלהיבו את הדגימה במהירות של 552 ננומטר לצורך הדמיה של mOrange. וב-638 ננומטר עבור DID בקרומי הגוב.ה-GUV mOrange-nano לא הצליחו להציג פלואורסצנטיות בחושך. עוצמת mOrange שכומתה בקרום ה-GUV הראתה גיוס חלבון מהיר ויעיל עם הפיכות מלאה.

morange-nano-recruitment-to-disilid-functionalized-giant-unilamellar

Research

JoVE Journal

Bioengineering

mOrange-Nano Recruitment to disiLID Functionalized Giant Unilamellar Vesicles (GUVs) for Generating Protein Patterns

181 Views.  University of Münster. כדי להתחיל, קח את הצינור של GUV שזה עתה נקטף. מוסיפים תמיסת סטרפטווידין, ומניחים לה לשבת במשך 30 דקות בטמפרטורת החדר. לאחר מכן הוסף מיקרומולר אחד של b-disiLID לתמיסת ה- GUV.כסו את הדגימה ברדיד אלומיניום ושמרו אותה בחושך. טפל בתא תחתון מזכוכית 18 באר מיקרו מגלשה עם 150 מיקרוליטר של תמ?...

Video: mOrange-Nano גיוס ל-disiLID Functional Giant Unilamellar Vesicles (GUVs) ליצירת תבניות חלבונים 

Dynamic Light-Induced Protein Patterns at Model Membranes

The precise localization and activation of proteins at the cell membrane at a certain time gives rise to many cellular processes, including cell polarization, migration, and division. Thus, methods to recruit proteins to model membranes with subcellular resolution and high temporal control are essential when reproducing and controlling such processes in synthetic cells. Here, a method is described for fabricating light-regulated reversible protein patterns at lipid membranes with high spatiotemporal precision. For this purpose, we immobilize the photoswitchable protein iLID (improved light-inducible dimer) on supported lipid bilayers (SLBs) and on the outer membrane of giant unilamellar vesicles (GUVs). Upon local blue light illumination, iLID binds to its partner Nano (wild-type SspB) and allows the recruitment of any protein of interest (POI) fused to Nano from the solution to the illuminated area on the membrane. This binding is reversible in the dark, which provides dynamic binding and release of the POI. Overall, this is a flexible and versatile method for regulating the localization of proteins with high precision in space and time using blue light.

Here, a protocol is described for generating light-regulated and reversible protein patterns with high spatiotemporal precision at artificial lipid membranes. The method consists of the localized photoactivation of the protein iLID (improved light-inducible dimer) immobilized on model membranes that, under blue light, binds to its partner protein Nano (wild-type SspB).