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<h1 class="text title" doc-editable="text" data-component-id="doc-1ef7l320d0">The TAC universe grows beyond PROTACs</h1><h2 class="title-bottom webtitle" doc-editable="title" data-component-id="doc-1ef7l34r60">Inducing autophagy is becoming a popular strategy as targeting chimeras extend beyond protein degradation</h2><div class="byline ng-tns-c17-4 ng-star-inserted" data-component-id="doc-1ef7l3fol0">
    <span class="ng-tns-c17-4" doc-editable="text">By Danielle Golovin, Staff Writer</span>
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Arvinas Inc.

Kymera Therapeutics Inc.

Vividion Therapeutics Inc.

Bayer AG

PAQ Therapeutics Inc.

Autotac Bio. Inc.

Frontier Medicines Corp.

Casma Therapeutics Inc.

Pin Pharmaceuticals Inc.

Lycia Therapeutics Inc.

University of California Berkeley

Genentech Inc.

Broad Institute of MIT and Harvard

Palleon Pharmaceuticals Inc.

Scripps Research

Expansion Therapeutics Inc.

Amgen Inc.

Dunad Therapeutics Ltd.

ATC-102

Cereblon (CRBN)

Microtubule-associated protein 1 light chain 3 beta (MAP1LC3B) (LC3B)

Sequestosome 1 (SQSTM1) (p62)

Huntingtin (HTT)

Macrophage migration inhibitory factor (MIF)

The TAC universe grows beyond PROTACs

Inducing autophagy is becoming a popular strategy as targeting chimeras extend beyond protein degradation.

Inducing autophagy is becoming a popular strategy as targeting chimeras extend beyond protein degradation

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