CALL FOR RESEARCH FELLOWSHIP Fellowship Reference GIMM-BI-37-2026

GIMM; Lisboa; Remote; EUR 12,000 - 15,000; Full time

Job summary

Gulbenkian Institute for Molecular Medicine (GIMM) invites applications for the NOS Alive – GIMM 2026 Research Fellowship to be carried out at the Daniel Fisch Lab. The project focuses on harnessing GBP1 in translational antimicrobial research and includes a 12-month, non-renewable fellowship starting January 2027.

The fellowship offers a monthly stipend of €1,090.98 (Bachelor) or €1,359.64 (Master), with social security and insurance coverage provided.

Qualifications

• Holder of a bachelor’s and/or master’s degree in biology or a related field (mandatory requirement), with the most recent degree completed after January 2022.
• Excellent command of spoken and written English.

Responsibilities

• The research work will be carried out at Daniel Fisch Lab.
• Fellowship stipend details and funding conditions apply as described (monthly stipend with specific amounts for bachelor’s vs master’s degree).
• Predicted start date is January 2027 for a period of 12 months on an exclusive, non-renewable basis.

Education

Biology degree (BSc/MSc)

Job description

Open Call for CALL FOR RESEARCH FELLOWSHIP Fellowship Reference GIMM-BI-37-2026

Gulbenkian Institute for Molecular Medicine (GIMM) opens a call for a Research Fellowship designated\" NOS Alive – GIMM 2026 Research Fellowship\", within the scope of the partnership established between the GIMM Foundation – Gulbenkian Institute for Molecular Medicine (GIMM) and Everything is New, the promoter of the NOS Alive. For this call, the GIMM Foundation is offering one research fellowship associated with the following research project. The research work will be carried out at the Daniel Fisch Laboratory. This fellowship is funded by Everything is New, under the following conditions:

Scientific Area(s):Biology and Life and Health Sciences

About the project at Daniel Fisch Lab

The innate immune system is our first line of defense against infection, providing immediate responses to a wide range of pathogens. It comprises physical barriers, soluble factors, and cellular components, which cooperate to control infections and influence adaptive immune responses. Innate immune cells recognize pathogens through pattern recognition receptors (PRRs) that detect conserved pathogen‑associated molecular patterns (PAMPs) and trigger inflammatory and antimicrobial responses. However, synthetic approaches to harness the therapeutic potential of innate immunity have largely remained unexplored. This is in stark contrast to mechanisms of the adaptive immune system, for example CAR‑T cells, which have already shown great potential in the clinic. This project aims to harness mechanisms of the innate immune system for translational applications. Specifically, we will investigate Guanylate‑Binding Proteins (GBPs); a family of interferon (IFN)–inducible GTPases that play a pivotal role in defense against intracellular pathogens. The GBPs belong to the dynamin superfamily and feature a globular GTPase domain and a flexible C‑terminal helical domain. They target intracellular pathogens and mediate their clearance by forming complexes which destabilize membranes and disintegrate pathogens. Interestingly, GBPs exhibit high specificity in targeting pathogens and lipid membranes thanks to their PRR‑like activity. For example, GBP1 recognizes lipopolysaccharide (LPS) in the outer membrane of Gram‑negative, cytosolic bacteria, disrupts the outer membrane and exposes the underlying bacterial structures to other immune effectors. While GBPs are primarily known for their intracellular functions, they can also be secreted via an unconventional pathway. The extracellular function of GBPs is unexplored but could have significant implications for understanding their role in systemic defense. The overarching goal of this project is to re‑purpose GBP1 as a broad‑ spectrum anti‑microbial drug against bacteria. Specifically, we want to: 1. Test the targeting activity of GBP1 against a large panel of bacteria and its influence on bacterial growth 2. Re‑engineer GBP1 into a vehicle that targets extracellular bacteria for clearance and stimulation of beneficial immune activities. To do so, we will express fluorescently tagged, farnesylated GBP1 (e.g. with hfYFP) in a bacterial (but LPS‑free) system with subsequent affinity purification. Normal protein functions will be tested in quality control experiments. Next, we will assemble a large panel of bacteria encompassing facultative and obligate extracellular/intracellular species. The final panel will include biologically diverse species with various types of LPS, capsulated and non‑capsulated as well as flagellated (i.e. motile) vs. immotile cells. Targeting by GBP1 will be tested in vitro, by mixing fluorescently labelled bacteria and GBP1 in presence or absence of GTP followed by microscopy analysis. The proportion of coated cells will be determined using automated image analysis and classification by AI computer vision models. We will further establish a microplate reader‑based high throughput growth assays for all bacteria and test the effect of GBP1 coating on bacterial growth and fitness. These data will be scrutinized by classical CFU assays. This line of experiments will establish the bacterial targeting spectrum of GBP1 and record its baseline antimicrobial activities. Next, we will turn GBP1 into a precision targeting vehicle for bacteria by engineering chimeric fusion proteins with novel functions. To promote bacterial clearance, GBP1 will be fused to immune effector domains that enhance opsonization, phagocytosis, complement activation, and potentially bacterial neutralization. To dampen harmful inflammation, GBP1 will be fused to a high‑affinity lipid A‑binding domain to mask LPS and limit PRR activation. These fusion proteins will be evaluated for antimicrobial, targeting, and immune‑modulatory activities with the ultimate goal of creating a single construct that promotes clearance of bacteria while preventing excessive inflammation.

Fellowship recipients / Admission requirements:Any National, foreign or stateless candidate that fulfils the necessary conditions to be enrolled in a non‑academic degree course (in area related to the work plan) can apply. Are considered “Non‑academic degree courses” the ones referred in paragraph e) of number 3 of article 4 of Decree‑Law nr 74/2006, from 24 th March, in its current version, as long as they are developed in association and cooperation between a higher education institution and at least one R&D Unit in accordance with the provisions of paragraph e) of Article 3 of FCT Fellowship Regulation.

Applicants must meet the following requirements:

• Holder of a bachelor’s and/or master’s degree in biology or a related field (mandatory requirement), with the most recent degree completed after January 2022;
• Excellent command of spoken and written English.

Predicted start date, duration and renewal conditions: The fellowship contract is predicted to start in January 2027, for a period of 12 (twelve) months on an exclusive basis, non‑renewable.

Workplace and Scientific orientation: The research work will be carried out in Daniel Fisch Lab.

Non‑discrimination and equal access policy: GIMM promotes a non‑discrimination and equal access policy, wherefore no candidate can be privileged, benefited, impaired or deprived of any rights whatsoever, or be exempt of any duties based on their ancestry, age, sex, sexual preference, marital status, family and economic conditions, instruction, origin or social conditions, genetic heritage, reduced work capacity, disability, chronic illness, nationality, ethnic origin or race, origin territory, language, religion, political or ideological convictions and union membership.

International environment and experience: Diversity is a fundamental aspect of the essence of GIMM, where researchers and non‑researchers of different nationalities, backgrounds and areas of study work together, promoting the exchange of experiences and interactions, contributing to the personal and professional development of each person and to the existence of an international, inclusive and stimulating environment.

Research Fellows Support Centre: The Research Fellows Support Centre is open every day from 09:00AM to 11:00AM at People & Culture Unit Office.

Fellowship financial conditions: The fellow will receive a monthly stipend of €1,090.98 (bachelor’s degree) or €1,359.64 (master’s degree), in accordance with the applicable regulations. The amount will be paid by wire transfer at the end of each month. The fellow will also benefit from a personal accident insurance to execute the proposed research activities as well as the right to Social Security through Voluntary Social Insurance regimen, if wanted, under the terms of Código dos Regimes Contributivos do Sistema Previdencial de Segurança Social and the respective contribution costs will be supported by the research project.

• Detailed CV;
• BSc and/or MSc certificate;
• One professional or academic reference;
• Candidate’s declaration of honor indicating previous fellowships, if any, its typology and duration.

The non‑compliance with these requirements determines the immediate rejection of the application.

Jury evaluation