Protein

— High Quality Drug Target Proteins

Membrane protein

Membrane proteins pose significant challenges in the field of structural biology, requiring substantial investments in terms of time and financial resources. However, the ability to quickly determine the most suitable expression system and purification conditions using minimal material can greatly reduce the initial research time and financial burden, thereby accelerating the early stages of a project.

At Biortus, we developed our small-scale workflows designed to facilitate membrane protein expression and purification screening. Here, we offer support in rapidly cloning and screening constructs simultaneously on a small scale (3-5ml of cell culture per condition) using various expression systems such as E.coli, yeast, insect or mammalian cell cultures. To expedite the process, we employ commonly used purification tags (e.g., His, FLAG, Twin-Strep, GST) and reporter proteins (e.g., eGFP, RFP, YFP, mStayGold) to quickly identify the most suitable expression and purification conditions. This includes optimizing factors such as incubation time and temperature, solvent composition, detergents, pH, salts, and other additives.

We assess the success of the screening process by utilizing techniques such as fluorescence size exclusion chromatography (FSEC), SDS-PAGE gels, Western Blot. To address the challenge of extremely low expression levels of membrane proteins, we have the capability to utilize anti-eGFP nanobody resin, which offers high specificity in capturing eGFP-tagged membrane proteins (with a dissociation constant, kd, of ~6 pM). We have successfully purified over 300 unique membrane proteins such as GPCR, ion channel, transporters by using this approach. We have a variety of membrane proteins available for purchase online. For more information, please contact us.

Construct design

Gene/GFP

Homolog screening;

Protein engineering;

Affnity tags & vectors;

N/C terminal truncation;

Loop deletion;

Mutagenesis;

Fusion partners (T4L,BRIL...);

Expression system

Insent cell/Mammalian

Insect cell expression: System: Bac to Bac
Cell: sf9, Sf21 & Hi5

Mammalian cell expression:
System: Transient Transfection; BacMam
Cell: Expi293F, Expi293F GnTI-

Small scale expression test

  • Fluorescence microscope

    Rapid expression screening

    Sub-cellular localization in host cell

  • Fluorescence size exclusion chromatography (FSEC)

    High-throughput screening monodisperisty for constructs and solubilization conditions

    Estimation of MPs overexpression level

    No need for purification

    Less than 5 ml expression media

  • Western Blot

    Confirm the expression of intact MPs

Large scale expression and purification

  • Anti-eGFP nanobody-based affinity purification

    Catch the eGFP-tagged protein with high specificity

    Higher purity than the TALON/Streptactin resin

    Need to cleave the eGFP tag

  • Purified membrane protein

    Downstream application:
    Nanodisc reconstitution
    SPR assay;
    TRIC assay;
    Activity determination;
    Thermal shift assay
    Structure determination;

  • GPCRs

  • lon channels

  • SLCs

  • ABC transporters

  • Other MPs

Our membrane protein production platform enables initial purification on a small scale, and also provide clients with the opportunity to screen a broader range of conditions. This includes, but is not limited to, detergents, amphipols, membrane scaffold proteins (MSPs), SMALPS, lipids, pH, and salts.
  • A2AR-nanodisc

  • ABC transporter X-SMALPs

  • ABCB10-Salipro

  • GlyRα3-amphipol

Quality control pipeline

  • Negative staining EM

  • LC-MS

  • Mass Photometry

Maintaining the functional integrity of purified membrane proteins is crucial for downstream applications. At Biortus, we offer a range of biochemical assays, such as ATPase assays for ABC transporters, as well as biophysical assays including thermal shift assays, surface plasmon resonance (SPR), and TRIC (temperature related intensity change) assays for the purified membrane proteins. These assays help assess the functionality and stability of the proteins, ensuring their suitability for further studies and applications.

ATPase assay for ABC transporters

ADP-Glo™assay

Phosphate detection assay

ATPase assay using 1mM ATP and purified ABC transporter in detergents

Biophysical assay-thermal shift assay

nanoDSF assay

CPM-based assay

Thermal shift assav usina purified ABC transporter in deteraents

Biophysical assay-SPR

SPR assay for A2AR

SPR assay for APJR

Biophysical assay-TRIC

TRlC( T emperature R elated I ntensity C hange)assay

Dianthus NT.23 Pico Duo

Compared to Traditional MST, TRIC:

Uses less protein

Allows more conditions (384wells)

Higher throughput

Done is as little as 30 min

Less background

At Biortus, we also specialize in Cryo-Electron Microscopy (Cryo-EM) studies of membrane proteins. Our expertise extends to the determination of various types of membrane proteins, including inactive state G-protein coupled receptors (GPCRs), active state GPCRs, ion channels, solute carrier proteins (SLCs), and ATP-binding cassette (ABC) transporters. By combining our expertise in Cryo-EM with other biochemical and biophysical assays, we can provide comprehensive insights into the structure and function of membrane proteins. This information is crucial for understanding their roles in cellular processes and for the development of targeted therapeutics.

If you have any specific questions or would like to discuss further, please let me know!
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